key: cord-0977763-k7kpbc7r
authors: nan
title: Abstracts from the Fourth Bioelectronic Medicine Summit: Technology Targeting Molecular Mechanisms: BEM, Virtual, 23-24 September 2020
date: 2020-12-23
journal: Bioelectron Med
DOI: 10.1186/s42234-020-00060-6
sha: b823ed19a7cbda50703865c382962e4f2c3955b2
doc_id: 977763
cord_uid: k7kpbc7r

nan

Transmural endoscopy for the purposes of performing per oral endoscopic myotomy (POEM) is a well-established and routine procedure for treating achalasia. During this procedure, an endoscopic tunnel is formed between the esophageal mucosa to the outer muscle layers, thereby gaining access to thoracic and abdominal cavities. Previously, we have shown that it is possible to identify and localize peripheral branches of the vagus nerve using commercially available endoscopes with digital/optical magnification and narrow band imaging. In this study, we explore the feasibility of recording nerve activity from the esophageal and gastric vagus branches within the abdominal and thoracic cavity in a swine model, by using transmural endoscopy. We will use custom-built nerve cuff and spiral electrodes that can be placed endoscopically to monitor for nerve activity and stimulate at different sites along the peripheral vagal branches. Additionally, we will also record the evoked compound action potentials (CAPs) in response to cervical and auricular vagus nerve stimulation applied directly on the nerve. Transmural endoscopy opens up the possibility of localizing and recording from the vagal nerve branches via a minimally invasive surgical procedure. Further studies are needed to explore its potential for delivering bioelectronic medicine.

Spinal cord injury (SCI) affects approximately 18,000 individuals every year in the United States, with over half of the cases resulting in upper limb impairment. Restoring hand movement and dexterity is one of the key, albeit largely unmet, priorities of SCI survivors. Recently, transcutaneous spinal cord stimulation (tSCS) in conjunction with activity-based training has shown considerable promise in improving motor performance of incomplete SCI patients. However, conventional tSCS training requires intensive physical therapy for long periods, typically 80 sessions. This is because conventional tSCS uses an all-or-none stimulation pattern that simultaneously activates multiple motor pools and hence, it requires a needlessly laborious effort to isolate multiple hand movements, which is not clinically viable. In this study we explore the effect of stimulation pattern and electrode area on targeting specific spinal nerves via tSCS for hand restoration. We have developed a custom transcutaneous neurostimulator with fatigue-resistant waveforms and high-density electrodes (FocalStim) that allow highly focalized activations of nerve fibers. Using FocalStim, we can generate individual or burst mode stimulation patterns, as well as, vary the electrode area from 100mm 2 to 1000mm 2 . Further, by recording hand movements and muscle activity through electromyogram recordings of both able-bodied and SCI participants during tSCS, we can potentially identify the optimal stimulation parameters and electrode sizes for targeting specific hand movements using tSCS. Future studies will explore automatic optimization of tSCS combined with intent-driven (through an implantable brain interface and noninvasive wearable sensing technologies) targeting of specific spinal nerves and its benefits on hand restoration.

Highly focal somatosensory percepts at fingertips evoked reliably by SEEG electrodes: an approach for sensory BCI Santosh Chandrasekaran 1 , Stephan Bickel 2,3,4 , Jose Herrero 2 , Noah Markowitz 2 , Elizabeth Espinal 2 , Kim Joo-won 5 Artificial somatosensory feedback is an important component for a sensorimotor brain-computer interface system that is intuitive to use and reduces dependence on visual feedback. For people with tetraplegia, targeted electrical stimulation of the somatosensory cortex has been used to provide somatotopically relevant sensory feedback. Currently, microelectrode arrays and electrocorticography (ECoG) grids are the most widely used modes of delivering such feedback through intracortical stimulation. These two kinds of electrode arrays are complementary in their advantages and deficiencies. While microelectrode arrays evoke highly focal percepts, they provide access to a very limited area of the cortex whereas ECoG grids provide a wider coverage of the cortex but evoke more diffuse percepts. In addition, neither approach can access the sulcal areas of the somatosensory cortex where the receptive fields pertaining to the fingertips are located in humans. Here, we reliably target the hand regions of the primary somatosensory cortex stereotactic electroencephalography (SEEG) depth electrodes guided by high-resolution fMRI and myelin maps. The SEEG electrodes allow us to access even the sulcal regions S1. We elicited highly focal sensory percepts in the fingers, including fingertips, and the hand. Using within-patient comparisons, we also show that percepts evoked by SEEG electrodes are more focal and can be localized to fingertips more often than those evoked by high density ECoG grid electrodes. Multi-conductor electrical leads are a critical and underappreciated aspect of implanted medical devices, and they represent one of the largest failure mechanisms for marketed devices such as DBS and VNS implants. We are developing a new helical lead with gold wires as part of a large NIH-funded program to develop and translate a new hearing prosthesis that uses a penetrating Utah array in combination with a marketed cochlear stimulator. The helical leads for this project are tested to confirm compliance with requirements for cochlear implants (e.g. AAMI/ ANSI CI86:2017), while safe and effective for use in the small clinical investigations. The mechanical tests are to evaluate lead performance for surgical use, minimize tethering forces, enable anchoring, and have sufficient fatigue resistance for our study. The helical leads joining the Auditory Nerve Utah Slanted electrode (AN-USEA) and the MED-EL Synchrony 2 stimulator pass the testing standards with expected biomechanical loads, in which are demonstrated with vigorous benchtop tests following a 10-day saline pre-soak and sterilization including: continuity, leakage current (<0.1 μA), bend testing (>100,000 bend cycles at ±15°and 2 Hz frequency), tensile testing to at least 10% elongation, and insulation test between channels in the wire bundle to have impedance values of >100 kΩ. The helical leads are exposed to representative stresses and have not shown signs of failure visually, electrically, nor mechanically which illustrates the robustness and flexibility of the leads. Consistent with standards for cochlear implants, the helical leads show to be a resilient and reliable component of cochlear devices.

A method to quantify autonomic nervous system function in healthy, able-bodied individuals Shubham Debnath, PhD 1 , Todd J. Levy, MS 1 , Theodoros P. Zanos, PhD The autonomic nervous system (ANS) regulates many physiological processes, since organs receive reciprocal input from the parasympathetic and sympathetic branches of ANS to maintain homeostasis. Dysregulation of the ANS can occur due to disorders or injury, including diabetes, sepsis, spinal cord injury, and other conditions. Development of quantitative biomarkers of ANS function can yield novel insights to such dysregulation and provide a useful tool to diagnose and assess the severity of these disorders. Such a metric was extracted here from physiological signals obtained by clinically standard techniques during controlled autonomic testing. Nineteen healthy, able-bodied individuals attended four sessions, each consisting of five autonomic tests; noninvasive sensors were used to capture continuous physiological data, including electrocardiography (ECG), blood pressure (BP), respiration, galvanic skin response, and pupil diameter. Raw ECG and BP signals were used to calculate heart rate, mean arterial pressure, and a heart rate variability measure, root mean square of successive differences (RMSSD) between heartbeats. Calculated signals were averaged by test and recording modality, and a template matching method was developed to characterize individual responses by determining features that represented duration and amplitude scales compared to the average response. As measured by the derived index, sympathetic amplitude responses significantly increased with higher body mass index among participants. Longer and larger sympathetic and longer parasympathetic responses were observed in afternoon testing, but larger parasympathetic responses were measured in morning testing sessions. Quantifying ANS function can provide crucial information about disease presence or intensity and treatment efficacy. TTFields are frequency-specific, alternating electrical fields developed for the treatment of cancer. They are delivered non-invasively to the tumor region using a home-use medical device. TTFields' mechanism of action is based on exertion of directional forces on polarizable microtubules, interfering with the assembly of the normal mitotic spindle. Such interference results in mitotic arrest, ultimately leading to cell death. To date, FDA has approved TTFields for recurrent and newly-diagnosed glioblastoma, and for mesothelioma. The only frequently-reported adverse event related to TTFields is skin irritation underneath the transducer arrays applied to the skin. Since their mechanism of action suggests anti-mitotic activity in many other solid tumors, TTFields have been successfully investigated in preclinical and pilot studies in additional cancers. They are currently investigated in phase 3 trials in pancreatic, lung and ovarian cancers, and in brain metastasis. Pilot trials are ongoing in gastric and liver cancers. The establishment of TTFields as a new treatment modality in oncology involved extensive multi-disciplinary research and development activities. The tight collaboration between physicians, biologists, physicists and engineers enabled the concept of targeting cancer cells with electric fields to become a therapy available at the clinic. This same collaboration continues to move the technology forward, with novel hardware and software advancements being implemented these days. They include more sophisticated design and materials, as well as treatment planning software for further improvements in treatment efficacy. These advancements make TTFields a more personalized modality, tuned to target the disease of an individual patient in the most effective way.

Targeted peripheral focused ultrasound stimulation attenuates obesity induced metabolic and inflammatory dysfunctions Tomás S. Huerta 1, 2 Obesity is associated with increased mortality and significant comorbidities, including insulin resistance, metabolic syndrome, and cardiovascular disease. Chronic low-grade inflammation is a hallmark of the pathophysiology of obesity. Recent studies have utilized noninvasive peripheral focused ultrasound stimulation (pFUS) to the liver to improve glucose metabolism in endotoxemia. Here we reasoned that pFUS of the liver may alleviate diet-induced obesity related inflammation and other comorbidities. After 16 weeks, obese mice that received daily hepatic pFUS, from weeks 9 to 16, had significantly decreased body weights compared to sham-stimulated mice on the same diet (P < 0.01, 2-way RM ANOVA). pFUS also significantly reduced adipokine levels (P = 0.05, 2-way ANOVA) and circulating lipids (P < 0.05, 2-way ANOVA) in obese mice. Hepatic pFUS significantly reduced liver inflammation observed with reduced cytokine levels (P < 0.001, 1-way ANOVA) and leukocyte infiltration (P < 0.0001, Kruskal-Wallis H test). Our findings demonstrate the efficacy of end-organ targeted focused ultrasound to the porta hepatis for alleviating diet-induced obesity and improving several aspects of metabolic health in mice. Our results highlight the possibility that hepatic focused ultrasound might be used as a novel noninvasive treatment for obesity. * These authors contributed equally Bioelectronic medicine depends on a detailed understanding of how signals within and between neurons, glia, and immune cells interact, along with their impact on organ health. A toolset that enables the simultaneous imaging of many signals in real-time would allow such signaling maps to be obtained, but classical imaging is limited by the number of fluorescent colors that do not overlap. We have invented a way to map potentially arbitrary numbers of signals within a single living cell by fusing a fluorescent reporter to a pair of self-assembling peptides. The reporters stably clustered within cells at random points, distant enough to be resolved by a microscope but close enough to spatially sample the relevant biology. The clusters, which we call signaling reporter islands (SiRIs), can be modularly designed to permit existing fluorescent reporters to be efficiently adapted for simultaneous measurement of many nodes in a signal transduction network within single living cells. We created SiRIs for indicators of second messengers and kinases and used them to image up to 5 signals at once in a single living neuron. Applied to hippocampal neurons in both culture and brain slice, we discovered relationships between the speed of calcium signaling and the amplitude of PKA cellular signaling, upon receiving a cAMP-driving cellular input. Thus, SiRIs will enable understanding the relationships between the components of molecular decision-making in immune cells, neurons, and other cell types. Being fully genetically encoded, SiRIs will hopefully become an easy-to-use component of the bioelectronic medicine development toolbox. **Co-senior authors with equal contribution Chinese studies reported predictors of severe disease and mortality associated with coronavirus disease 2019 (COVID-19). A generalizable and simple survival calculator based on objective data from US patients hospitalized with COVID-19 has not yet been introduced. Our goal was to develop and validate a clinical tool to predict 7-day survival in patients hospitalized with COVID-19. We used electronic health record data of 13027 adult patients hospitalized with a confirmed diagnosis of COVID-19 from thirteen acute care hospitals in the New York City area, 12 of which were part of Northwell Health. Demographic, laboratory, clinical, and outcome data were extracted from the electronic health records. Optimal predictors and performance were identified using least absolute shrinkage and selection operator (LASSO) regression with receiver operating characteristic curves and measurements of area under the curve (AUC). Serum blood urea nitrogen, age, oxygen saturation, serum sodium, red cell distribution width, and absolute neutrophil count were identified as the 6 optimal of 41 possible predictors of survival. These factors constitute the NOCOS (Northwell COVID-19 Survival) Calculator. Performance in the prospective validation and external validation were marked by AUCs of 0.80 ([0.75, 0.84] 95% CI), and 0.78 ([0.75, 0.80] 95% CI), respectively. Collectively, the NOCOS Calculator uses 6 factors routinely available at hospital admission to predict 7-day survival for patients hospitalized with COVID-19, and outperforms existing calculators like SOFA (p < 0.05 internal prospective validation) that are not specifically designed for COVID-19. The calculator is publicly available at https://feinstein.northwell.edu/NOCOS.

Trigeminal nerve stimulation induced hemodynamic oscillation confers neuroprotection for combined traumatic brain injury and hemorrhagic shock 

Combined traumatic brain injury (TBI) and hemorrhagic shock (HS) (TBI+HS), is associated with high levels of morbidity and mortality. The current resuscitative approach to TBI+HS involves intravascular volume expansion, vasopressors, and oxygen supplementation which requires access to medical care and yet inadequately address the severe hypoperfusion that distinguishes this condition. For decades, large spontaneous oscillations in blood pressure (BP) and cerebral blood flow (CBF) have been observed in individuals with high tolerance to hypovolemia. These hemodynamic waves represent an endogenous physiologic mechanism that improves cerebral perfusion and confers protection to cerebral tissue. In the present study, we explored the ability of electrical trigeminal nerve stimulation (TNS) to mimic the hemodynamic oscillations shown in individuals with high hypovolemia tolerance, and investigated its beneficial effects in a rat model of TBI+HS.

TBI+HS was induced by controlled cortical impact, and subsequent pressure-controlled HS (27±2 mmHg) for 35 minutes in male Sprague-Dawley rats. TNS induced large, synchronized oscillations in BP and CBF. These bio-mimicked hemodynamic oscillations attenuated the severity of brain injury, improved the survival rates, and facilitated functional recovery after TBI+HS. Secondary oscillations of P br O 2 reduced hypoxic stress as confirmed by HIF-1a expression in the hippocampus. Furthermore, non-specific TNS did not induce hemodynamic oscillations and did not show any the beneficial effects in this animal model of TBI+HS. Conclusions Bio-mimicked synchronized fluctuations of BP and CBF, and secondary oscillations of P br O 2 can be induced by specifically calibrated TNS to provide rapid pre-hospital treatment and improve survival outcomes following TBI+HS. * These authors contributed equally to this work Vagus nerve stimulation (VNS) is an emerging bioelectronic therapy with the potential to treat a wide range of conditions in which inflammation is implicated. Anti-inflammatory actions of VNS require norepinephrine (NE) release into the spleen by postganglionic neurons in abdominal ganglia. Real-time detection of NE could provide a marker to calibrate and optimize VNS antiinflammatory effects in individual subjects. Here, we describe a method to study in vivo VNS-elicited NE release in the spleen, using fast scan cyclic voltammetry (FSCV). Initially, NE oxidation potential was determined in vitro to be approximately 0.6 V, using standard cycling parameters. In experiments in anesthetized mice instrumented with ECG, a carbon fiber voltammetry electrode was inserted into the exposed spleen. VNS was delivered using a bipolar cuff electrode placed on the left cervical VN. Short trains of VNS (2-10 s duration, 100 μs pulse width) induced a peak oxidation current at 0.6 V indicating NE release at pulsing frequencies >5Hz (N=8 animals). NE currents were detected <10 s after VNS onset, peaked at 20-30 s, and returned to baseline within 1 to 10 min (N=5). Peak NE oxidation current was proportional to VNS intensity and to the concomitant VNS-elicited reduction in heart rate (N=3). These preliminary findings indicate that FSCV may be a reliable method for the real-time measurement of NE release in the spleen, thereby providing an in vivo marker of anti-inflammatory effects of VNS.

The effect of focused ultrasound neuromodulation of the liver on glucose metabolism in healthy mini-pigs Qanud K 1 , Tomaio J 1 , Song W 1 , Hagve M 2 , Gjessing P 2 , Al-Abed Y 1 Recently, focused ultrasound (FUS) neuromodulation was shown to have organ-specific effects in rodents undergoing acute inflammation, including a decrease in blood glucose levels when targeting the liver (Cotero V et al, Nature Comm 10: 952, 2019). It is unclear whether FUS has similar metabolic effects in large animals with similar anatomy and physiology to humans, in the absence of inflammation. In healthy mini-pigs, we validated whether FUS targeting the porta hepatis (PH) of the liver could lead to changes in glucose metabolism. First, in a series of hyperinsulinemic-euglycemic clamp experiments, we used different insulin infusion rates (IIRs) and determined the glucose infusion rate that achieved an euglycemic equilibrium (eGIR), a measure of insulin sensitivity independent of blood glucose levels. We found that measures of insulin sensitivity were larger at low IIRs ("unsaturated") than at high IIRs ("saturated"). Then, in a second series of experiments, eGIR was determined during low and high IIRs, before and after 4-min-long FUS of the PH. Sensory vagus nerve fibers transmit information in the form of action potentials to the central nervous system to maintain immunological homeostasis. Pro-inflammatory molecules including LPS, TNF, and IL-1β induce cytokine specific electrophysiological changes in vagus nerve signaling. In addition, these pro-inflammatory molecules directly activate nodose ganglion neurons, the location of sensory vagus nerve cell bodies. Previous studies have shown cytokines have a direct impact on cation channels TRPV1 and TRPA1, which are expressed on sensory fibers of the vagus nerve. Reasoning that these cation channels may play a role in vagus nerve mediated cytokine signaling we explored TRPA1's role in IL-1β induced vagus nerve activity. Extra neural electrical activity was recorded from the cervical vagus nerve in response to i.p. administration of IL-1β. IL-1β induces a significant increase in vagus nerve activity in wild type mice, however this response was ablated in whole body TRPA1 KO mice as well as neuronal specific TRPA1 KO mice (SynCre-TRPA1flox). Using calcium imaging and whole cell patch clamp recordings, we observed nodose ganglion neurons deficient in TRPA1 do not respond to IL-1β application. In addition, IL-1β induced calcium influx was inhibited by administration of the TRPA1 antagonist AM0902. These results elucidate a novel role for the TRPA1 cation channel as a necessary component for IL-1β induced vagus nerve signaling. Micro-fabricated polyimide (PI)-based neural electrodes have been actively pursued with innovations including electrode materials, architectures, microfabrication processes, and seamless integration with nervous tissues. Mouse vagus nerve (~100 μm) is a key therapeutic and research target in the field of bioelectronic medicine. However, the technology to interface delicate nerves for chronic endpoints has been a challenge. In this study, a PI flexible neural Flex electrodes with Ir/IrO x electrode sites was fabricated via a microelectromechanical system (MEMS) process, and an integration strategy was developed for the chronic interface with the mouse vagus nerve, including an epoxy reinforcement for the joints between electrode bonding pads and platinum wire leads, and a thermoforming process to shape the Flex electrodes for intimiate contact with the nerve. The electrochemical properties of the flex electrode, such as impedance and charge storage capacity (CSC), were characterized using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV), respectively. The impedance of the Flex electrode at 1 kHz was as low as 617.15 ± 13.17 Ω. The impedance spectra were fitted with an equivalent circuit model to clarify the electrode-electrolyte interface. Compared to the state-of-the-art with respect to the neural electrode with IrO x stimulation sites, the Flex electrode developed in this study has the CSC of 17.02 ± 3.04 mC/cm 2 . This study represents one of dedicated efforts to develop the chronic mouse vagus nerve interface, using microfabricated electrodes. Quantitative descriptions of the morphology and structure of peripheral nerves is important for bioelectronic and brain-machine interface devices. While histological procedures and microscopy techniques yield high-resolution detailed images of individual axons, automated methods to extract relevant information at the single-axon level are not widely available. We implemented a computer vision segmentation algorithm that allows for subsequent feature extraction in immunohistochemistry (IHC) images of peripheral nerves at the single fiber scale. These features include short and long cross-sectional diameter, area, and perimeter, thickness of surrounding myelin and polar coordinates of single axons within a nerve or nerve fascicle. To improve the performance of our computer vision algorithm, we generated a dataset of segmented immunohistochemical images and trained a deep convolutional neural network (Mask R-CNN) on instance segmentation. The dataset of segmented examples was produced by the original algorithm and subsequently refined by human annotators, yielding a significant 4-fold decrease in human labor compared to the process of manual annotation from scratch. A combined solution of the original algorithm and the deep convolutional neural network achieved a single-axon detection accuracy of 98%, as opposed to 82% using the traditional computer vision algorithm alone, on a held-out nerve section of 36 fascicles of the swine cervical vagus. Electrical stimulation of the vagus nerve inhibits expression of proinflammatory cytokines, such as tumor necrosis factor (TNF), through a neural circuit termed the inflammatory reflex. To determine whether vagus fiber populations could be selectively activated to control inflammatory and physiological function, we created ChAT-ChR2-eYFP, TRPV1-ChR2-eYFP, and VGlut2-ChR2-eYFP mice expressing lightsensitive channelrhodopsin-2 (ChR2) in specific neuronal and fiber populations. Utilizing in situ cervical vagus nerve preparations, we optogenetically stimulated vagal fibers (opto-VNS) with the following parameters: 470 nm, 1000 mA, 10 Hz, 50 ms, 5 min. After stimulation mice were then injected i.p. with lipopolysaccharide (0.3 mg/kg) to induce acute endotoxemia, then killed 90 mins later. Serum TNF was measured by ELISA. We observed that in a subset of ChAT-ChR2 mice, opto-VNS significantly decreased levels of TNF compared to sham-matched controls (t-test, P<0.02). Opto-VNS did not change TNF levels in TRPV1-ChR2 or VGlut2-ChR2 mice compared to shamstimulated controls. We also found that opto-VNS induced varying degrees of transient bradycardia in all three strains: ChAT-ChR2 ( The nervous system and the immune system are the two major organs of memory and host defense. Sensory neurons have been implicated in enhancing neurological memory, but whether neurons participate during immunity to novel antigens is unknown. Here, we show that TRPV1 expressing neurons are required to develop an antigen specific immune response and that direct activation of TRPV1+ signals by selective optogenetic stimulation enhances this response to novel antigen. We generated TRPV1-Cre/Lox-stop-lox diphtheria toxin A (TRPV1-DTA) mice to specifically ablate TRPV1 expressing neurons. TRPV1-DTA mice were subjected to immunization with keyhole limpet hemocyanin (KLH) and antigen-specific antibody responses were measured over 28 days. KLH-specific antibody responses were significantly blunted in TRPV1-DTA mice as compared to wild-type controls for 28-days post immunization. Next, we optogenetically activated TRPV1 neurons during immunization. TRPV1-Cre/Rosa-ChannelRhodopsin2 (TRPV1-ChR2) mice received optical stimulation on the dorsum of the paw with blue light immediately prior to a local immunization of KLH. Direct optogenetic stimulation of TRPV1+ neurons significantly increased KLH-specific antibody responses as compared to wild-type mice. Collectively these findings reveal that TRPV1-expressing sensory neurons modulate antigen-specific immune responses. This is the first genetic and selective functional evidence that nociceptors are required during immunization to produce antigen-specific antibodies. The goal of this work is to (1) create pipelines for entity data extraction using multiple medical NLP tools, (2) extract the signs and symptoms from an EHR (Electronic Health Records) corpus via this pipeline, and (3) compare results from the pipeline with manual annotations by clinicians. The NLP tools chosen for comparison in this particular study are CTAKES and CLAMP. Software pipelines based on Java and Python were built to process health records via these tools. Signs and symptoms that were extracted via these tools as XMI files were then standardized using Python-based data extraction techniques. The resulting signs and symptoms were further classified as positive (present), and negative (absent) by the tools. Clinicians also created a manually annotated ground truth to enable quantitative analysis of accuracy of each tool. The Jaccard (dice coefficient) was used to determine the degree of overlap between the 2 NLP tools and 3 annotators, resulting in a 2-by-3 matrix of values. For each tool-annotator comparison, the Jaccard coefficient was computed on a per-record basis and then averaged. For a single record, the overlap across each sign/symptom entity was averaged to get a recordlevel score. As a result, the NLP tools were evaluated against a manual ground truth and baseline performance metrics were extracted. In the future, this work could enable analysis and accuracy comparison of various NLP tools for the purpose of a variety of entity recognition purposes from health records, as was done with signs and symptoms in the case above. The development of modern bioelectronic therapeutics frequently relies upon in vivo studies of the physiological effects of neurostimulation. Numerous disease models available in small rodents provide ideal research settings; however, developing implants for small animals with cm-sized anatomies poses a technological challenge. Size constraints derive from limits on the energy capacity of ultraminiature batteries, integration of electrical circuits, and the need for resilient biocompatible packaging. While commercial medical devices offer multi-year lifetimes, devices for animal research typically target shorter lifetimes of weeks to months in order to reduce their volume, mass, and cost. Previously, our lab has demonstrated a novel constant-current neurostimulator providing basic control of stimulation parameters. We present an updated, fully-wireless design that utilizes near-field communication for dynamic control, enabling precise control of stimulation and more sophisticated experiments, as well as improved output characteristics. The device offers 0-3 mA amplitude, as short as 100 μs pulses, and frequency from DC to 10 kHz. Data from acute and chronic experiments validate the core functionality in the mouse model. Preliminary results suggest a usable lifetime longer than one month. Vertebrates control homeostasis during infection or injury by balancing the activity of pro-and anti-inflammatory responses. Reflex neural circuits inhibiting inflammation are well established, but the role of neurons stimulating inflammation is not clear. High mobility group box 1 (HMGB1), an established mediator in both infectious disease and sterile injury, is abundantly expressed in neurons. To elucidate the role of neuron-derived HMGB1 in neurogenic inflammation and nociceptive response, we generated neuronal-specific conditional HMGB1 knockout mice. Selective silencing of HMGB1 in neuronal tissues attenuates neurogenic inflammation in animal model of sciatic nerve chronic constriction injury (CCI). Genetic silencing of neuronal HMGB1 attenuated local HMGB1 expression, as well as CXCL1, IL-18 and TNF levels in the inflamed paws as compared to HMGB1 flox or wild type control mice. Sciatic nerve CCI-induced hyperalgesia (assessed by mechanical hypersensitivity via the von Frey test) was inhibited in the neuronal-HMGB1 deficient mice. Administration of anti-HMGB1 monoclonal antibodies conferred significant protection against sciatic nerve CCI-induced mechanical and thermal hyperalgesia. Furthermore, in collagen antibody-induced arthritis (CAIA), genetic silencing of neuronal HMGB1 significantly inhibited CAIA-induced joint edema formation, hyperalgesia and inflammatory cell infiltration as compared to CAIA in HMGB1 flox and wild type controls. Collectively, these findings reveal a previously unrecognized critical role for neuronal HMGB1 in initiating inflammation and nociceptive responses in the sciatic nerve CCI and CAIA models.

Optoelectronic medicinenongenetic means of nerve cell regulation with light Eric Daniel Głowacki, PhD 1,2 1 Laboratory of Organic Electronics, ITN Campus Norrköping, Linköping University, SE-60174, Norrköping, SE; 2 Central European Institute of Technology, Brno University of Technology, Purkynova 123, 61200 Brno, CZ Bioelectronic Medicine 2020, 6(Suppl 1):S1.

A great demand exists for minimally-invasive neuromodulation technologies to enable next-generation bioelectronic medicine. We report on our developments of ultrathin (opto)electronic devices for neurostimulation. All of these devices rely on far red/near infrared irradiation in the tissue transparency window to actuate nanoscale organic semiconductor components. Our flagship technology is the organic electrolytic photocapacitor (OEPC)a device that mimics biphasic current-pulse neurostimulation and thus transduces an optical signal into directly-evoked action potentials in neurons. These devices are not only wireless, but also 100-1000 times thinner than existing technologies. We will discuss chronic implants capable of stimulating peripheral nerves (sciatic and vagus) when actuated from outside of the body using diode lasers. Light power can be safely and effectively transmitted to implants up to 15 mm below the skin surface. We have observed stable operation in rodent models for at least 100 days. We believe that the combination of deep red light and ultrathin photovoltaic devices can account for a new paradigm in wireless bioelectronic medicine. Reliable recording and modulation of excitable tissue using implantable electronic devices have implications in diagnosing and treating many types of diseases. The advent of flexible electronics has enabled new concepts in interfacing devices with soft tissues. However, to date, most flexible electronics achieve mechanical compliance by using substrates composed of thin curable resins or elastomers. These materials are suboptimal for tissue interfacing because they: (1) exhibit Young's moduli that are orders of magnitude larger than many excitable tissues, such as peripheral nerves; (2) are difficult to integrate with hydrated tissue in vivo. Here I will present recent advances in materials and fabrication from our lab to address current limitations in flexible electronics. Specifically, the synthesis and formulation of adhesive hydrogels and transfer printing to create ultracompliant peripheral nerve interfaces will be described. Details regarding the in vitro and in vivo performance of ultracompliant electronics will be presented. Future prospective applications for this concept will also be highlighted, too.

Communicating with the nervous system for the cure of diseases Martin Schuettler CorTec GmbH, Freiburg, DE Bioelectronic Medicine 2020, 6(Suppl 1):S3.

CorTec develops a chronically implantable brain-computer interface called "Brain Interchange" for bi-directional communication with the brain. The system consists of various components: cortical grid electrodes, implantable electronics protected by ceramic hermetic package and body-external transceiver that communicates wirelessly with the implant and also wirelessly supplies the implant with energy via an inductive link. The system streams neural data from 32 electrode contacts to a computer where the data is processed and stored. Based on the incoming neural data, algorithms on the computer can take decisions on therapeutic actions, e.g. sending a stimulation command wirelessly to the implant which then delivery electrical pulses via the implanted electrodes to the brain, modulating brain activity. This closed-loop system can be used for patient-individual and situation-specific brain therapy, treating a variety of central nervous system related disorders. The system can also be used as bidirectional communication tool between brain and computer. Besides the development of Brain Interchange as a platform for central nervous system related therapy discovery and brain-machine interface studies, CorTec provides the innovative technology that permitted building the individual components of Brain Interchange to others. Especially the technology for producing lasermicromachined neural electrodes that permit high production precision while using only traditional implant materials such as medical grade silicone rubber and PtIr noble metal foil is applied to wide range of applications, also in the field of spinal cord stimulation and peripheral nerve interfacing, in preclinical as well as in clinical studies. Another technology made available to others is a ceramic hermetic package for electronic implant circuits that permits a very high number of electrical feedthroughs (100s) while providing excellent hermeticity. With these and other technologies, CorTec is dedicated to improving the field of neurotechnology and neural therapy discovery.

Targeting populations of fibers in clinically-relevant vagus nerve stimulation Stavros Zanos, MD, PhD

Atherosclerosis is a chronic nonresolving inflammatory disease of medium-and large-sized arteries causing heart attacks and strokes. As atherosclerotic plaques in the inner intimal layer and aortic media of these arteries lack nerve fibers, the impact of innervation on atherosclerosis remains unknown. However, nerves use the adventitia as their primary conduit to reach target tissues. We and others characterized artery tertiary lymphoid organs (ATLOs) in the aorta adventitia of apolipoprotein E knock-out mice and also found such aggregates in human diseased coronary arteries and other arterial tree segments. In view of these observations, we postulated that the peripheral nervous system may interact with diseased arteries via adventitial immune cells. We found in aged hyperlipidemic mice and in human atherosclerotic tissues that widespread neuro-immunecardiovascular-interfaces (NICIs) establish atherosclerosis-brain circuits (ABCs) capable of sensing and affecting atherosclerosis: (i) ATLOs interact with the peripheral nervous system (PNS) by stimulating axon growth; (ii) the adventitia is innervated by the sensory and sympathetic NS but not by the parasympathetic NS system; (iii) the adventitia is wired directly to the brain stem through lower thoracic dorsal-root-ganglia and sympathetic perivascular ganglia; (iv) advanced atherosclerosis is associated with increased nerve activities in splenic and celiac vagus nerves; and (v) elimination of the sympathetic NS disrupts ATLOs, attenuates atherosclerosis progression, and reduces plaque vulnerability. Our data demonstrate the pathophysiological relevance of NICIs in atherosclerosis and that the PNS employs NICIs to assemble ABCs. We hypothesize that intervention into neural circuits creates multiple unexpected opportunities to treat atherosclerosis.

Neural control of immunity in hypertension Daniela Carnevale, PhD University di Roma, Rome, IT Bioelectronic Medicine 2020, 6(Suppl 1):S6.

The nervous system and the immune system share the common ability to exert gatekeeper roles at the interfaces between internal and external environment. Although interaction between these two evolutionarily highly conserved systems is long recognized, the investigation into pathophysiological mechanisms regulating their reciprocal cross-talk has been the object of pathbreaking immunology and neuroscience research only in recent decades. In the last years, our group elucidated how the autonomic nervous system controls the splenic immunity recruited by hypertensive challenges. In this lecture, I will focus on the molecular mechanisms that regulate the neuro-immune crosstalk in hypertension. I will elaborate on the mechanistic insights into this brain-spleen axis led us uncover a new molecular pathway mediating the neuroimmune interaction established by noradrenergic-mediated release in the spleen of placental growth factor (PlGF), an angiogenic growth factor potentially targetable with pharmacological approaches.

Personalized bioelectroceutical modulation of carotid sinus nerve: a novel approach to treat type 2 diabetes Silvia V. Conde, PhD CEDOC, NOVA Medical School, Faculdade Cinecias Médicas, Universidade NOVA de Lisboa, Lisboa, PT Bioelectronic Medicine 2020, 6(Suppl 1):S7.

It is consensual that increased carotid body (CB) activity contributes to the sympathetic overactivation that characterizes essential hypertension, hypertension associated with obstructive sleep apnea and chronic heart failure (1). Additionally, we described that CB dysfunction is in the genesis of metabolic diseases via sympathetic nervous system overactivation (2, 3) . The CBs are arterial chemoreceptors that sense changes in blood O2, CO2, and pH levels. Apart from ventilatory control, the CBs have been reported to act as metabolic sensors being implicated in the control of energy homeostasis. We have recently described that CB activity is increased in animal models of metabolic disease (2, 4) and in prediabetes patients (5) . Also, we showed that abolishment of CB activity via bilateral resection of CB-sensitive nerve, the carotid sinus nerve (CSN), or via CB ablation in animals prevents and reverses dietinduced insulin resistance and glucose intolerance as well as sympathoadrenal overactivity, meaning that the beneficial effects of decreasing CB activity on glucose homeostasis are modulated by target-related efferent sympathetic nerves, through a reflex initiated in the CBs (2, 3, 6) . In agreement with our pre-clinical data, we described that hyperbaric oxygen therapy, that dramatically reduces CB activity, improves glucose homeostasis in type 2 diabetes (T2D) patients (7). Unilateral and/or bilateral CB surgical ablation has been also proposed as therapeutic option for sympathetic-mediated diseases. However, despite the promising results, neither hyperbaric oxygen therapy nor surgical CSN resection are optimal therapeutic approaches for CB-mediated diseases, as these procedures entail several side effects. My team recently showed that electrical modulation of the CSN restores glucose homeostasis in T2D animals implying that bioelectronic medicines might be suitable and selective therapeutic strategy for metabolic diseases. The present talk will provide a state-of-the-art update on the mechanisms of sensory transduction, neural circuitry, and reflex regulation of CBs chemoreceptor in metabolic diseases and will discuss the recent findings showing the efficacy of continuous kilohertz frequency alternative current device implanted on the CSN to reverse clinical features of T2D in rats (6) as well as the use of CSN neural recordings to detect metabolic information (8) that could be used for closed-loop control of CSN neuromodulation.

Artificial intelligence and machine learning are methods by which a computer system can generate complex, non-linear algorithms from data inputs that have the potential to be more accurate and deployed in real-time. In bioelectronics medicine, there are multiple pieces of complex electrophysiologic data that are acquired. While traditional diagnostic and therapeutic responses from these data are, by necessity, based on relatively simple models, the use of artificial intelligence may allow for the creation of more dynamic and complex responses that better mirror how normal human physiology responds to these electrical impulses. In the field of cardiac electrophysiology, for example, it has been demonstrated that, using a standard 12-lead electrocardiogram, it is possible to detect several diseases that are not apparent according to traditional interpretation methods, such as the risk of having a low ejection fraction, atrial fibrillation, or hypertrophic cardiomyopathy. In turn, dynamic, closed loop feedback systems that integrate several pieces of electrophysiologic data and determine appropriate responses that mirror physiologic needs may be feasible. Future research will focus on how bioelectronics data may be aggregated, used to build predictive algorithms, and how these algorithms may be integrated into diagnostic and therapeutic systems to advance bioelectronic devices.

Organic bioelectronics operating at the speed and resolution of neuronal signalling Magnus Berggren, PhD Department of Science & Technology, Laboratory of Organic Electronics, Linköping University, SE Bioelectronic Medicine 2020, 6(Suppl 1):S9.

Organic electronic materials are unique as the signal translator across the biology-technology gap. These biocompatible materials are also easily complexed with polyanions, polycations and functional biomaterials and can be included in various device architectures to form flexible, stretchable and even gelled device systems. Such organic bioelectronics can then process electronic, ionic and charged biomolecules in combination. These combined features make organic electronic materials unique in many aspects as the recorder and actuator of various functions and physiology of biological systems. A brief review of some of the recent achievements from the Laboratory of Organic Electronics is here given. In the BioComLab technology platform various organic bioelectronic sensors and actuators are combined with communication technology to form a body area network for future healthcare applications. Various sensors are included within electronic skin patches, then connected to electronic drug delivery components via capacitive body-coupled communication. This system provides sensoractuator feedback and improves its decision-making performance using deep-learning protocols provided from cloud connectivity. With the Bio-ComLab platform we target an array of neuronal disorders and diseases, such as epilepsy, Parkinson's disease and chronical pain. A sphincter is a ring like muscle that normally maintains constriction of a body passage or orifice and that relaxes as required by normal physiological functioning. Sphincters are control mechanisms in the gastrointestinal tract. They control forward passage and prevent or allow the backwards passage of solids, liquids and gases. Direct electrical stimulation of the sphincter can lead to contraction while stimulation of the Vagus Nerve can lead to contraction or relaxation of the sphincter, depending on the parameters of stimulation. Currently most vagal nerve stimulation is performed at the level of the Cervical Vagus Nerve. This stimulation leads to specific targeted physiologic effects at the expense of other untargeted physiologic effects. We propose stimulating peripheral branches of the vagus nerve near the target organ to more precisely target desired specific physiologic effects without the unwanted physiologic effects. We have developed tunneling techniques in a porcine model in which a Z tract is created within the submucosal space of the esophagus, stomach, small intestine or colon. These techniques can be used to access peripheral branches of the Vagus Nerve in order to place electrodes and more precisely target beneficial effects of nerve stimulation while eliminating unwanted effects. Through the esophagus one can reach vagal branches to lungs, heart, esophagus, and stomach. Through the stomach one can reach vagal branches to stomach, liver, pancreas, kidneys, small intestine, spleen and colon. We have also developed the use of endoscopic ultrasound, in a porcine model, to direct needle electrodes to target, access and stimulate nerves and ganglion within the Celiac, Superior Mesenteric and inferior Mesenteric Plexus. Using FLIP technology to evaluate the contraction and relaxation of the pyloric sphincter and the lower esophageal sphincter we have demonstrated both contraction and relaxation of these sphincters using direct electrical stimulation of muscle and indirect electrical stimulation of the vagus nerve. We believe that these techniques may be used in the future to access and stimulate peripheral branches of the Vagus Nerve to treat many diseases including, chronic hypertension, diabetes, gastroesophageal reflux disease (GERD), gastroparesis, end stage congestive heart failure (CHF), end stage pulmonary disease such as pulmonary hypertension, asthma, diabetes, renal failure, IBD, other inflammatory diseases and obesity, as well as diseases related to dysfunction of gastrointestinal sphincters.

Portuguese Foundation for Science and Technology

Oreal/FCT/Unesco Medals S8. AI and bioelectronic medicine: A vision for future research and collaboration Suraj Kapa

Visual cortical prosthetics: The next generation Daniel Yoshor, MD University of Pennsylvania, Philadelphia, PA, US Bioelectronic Medicine 2020, 6(Suppl 1):S11.This abstract from this presentation is adapted from the following publication: Beauchamp MS, Oswalt D, Sun P, Foster BL, Magnotti JF, Niketeghad S, Pouratian N, Bosking WH, Yoshor D. Dynamic Stimulation of Visual Cortex Produces Form Vision in Sighted and Blind Humans. Cell. 2020;181(4):774-83 e5. Epub 2020/05/16. doi: 10.1016/ j.cell.2020.04.033. PubMed PMID: 32413298; PMCID: PMC7331799. A visual cortical prosthesis (VCP) has long been proposed as a strategy for restoring useful vision to the blind, under the assumption that visual percepts of small spots of light produced with electrical stimulation of visual cortex (phosphenes) will combine into coherent percepts of visual forms, like pixels on a video screen. In prior decades, a number of research teams tested early prototypes of a VCP, but these efforts were limited by the technology of the day. The remarkable advances in computer science and engineering have spurred a renewed interest in developing VCPs that is now well underway. In this presentation I review past and ongoing work in developing VCPs. In addition, I highlight the challenges involved in using phosphenes as combinatorial elements, and describe an alternative strategy in which shapes are traced on the surface of visual cortex by stimulating electrodes in dynamic sequence. In our experience testing both sighted and blind participants, dynamic stimulation enabled accurate recognition of letter shapes predicted by the brain's spatial map of the visual world. Forms were presented and recognized rapidly by blind participants, up to 86 forms per minute. These findings demonstrate that a brain prosthetic can produce coherent percepts of visual forms. The α7 nicotinic acetylcholine receptor (α7nAChR) is central to the anti-inflammatory function of the vagus nerve in a physiological mechanism termed the inflammatory reflex. Studies on the inflammatory reflex have been instrumental for the current development of the field of bioelectronic medicine. An independent investigation of the biological role of αB-crystallin (HspB5), the most abundant gene transcript present in active multiple sclerosis lesions in human brains, also led to α7nAChR. Induction of experimental autoimmune encephalomyelitis (EAE) in HspB5−/− mice results in greater paralytic signs, increased levels of proinflammatory cytokines, and T-lymphocyte activation relative to wild-type animals. Administration of HspB5 was therapeutic in animal models of multiple sclerosis, retinal and cardiac ischemia, and stroke. Structure-activity studies established that residues 73-92 were as potent as the parent protein, but only when it formed amyloid fibrils. Amyloid fibrils and small heat shock proteins (sHsps) selectively bound α7nAChR on peritoneal macrophages (MΦs) and B lymphocytes, converting the MΦs to an immune suppressive phenotype and mobilizing the migration of both cell types from the peritoneum to secondary lymph organs. Finally, our approach in translation to the clinic is for the development of small molecules that are orally active to modulate the α7nAChR.Other speaker talks Bioelectronic Medicine 2020, 6(Suppl 1):S12. S13. SPARC, Data and tools from the NIH SPARC program to catalyze the development of next-generation therapeutics Gene Civillico, PhD National Institutes of Health Bioelectronic Medicine 2020, 6(Suppl 1):S13.

Designing new materials for Bioelectronics applications Molly M. Stevens, PhD Imperial College London Bioelectronic Medicine 2020, 6(Suppl 1):S14.

Non-invasive neuromodulation using ultrasound: A work in translation Chris Puleo, PhD General Electric Bioelectronic Medicine 2020, 6(Suppl 1):S15.

Technologies and therapies to enable persons with neurological injuries to reach their full potential Robert Rennaker, PhD University of Texas at Dallas Bioelectronic Medicine 2020, 6(Suppl 1):S16.

Neuroimmune cardiovascular interfaces form atherosclerosis brain circuits Saroj Mohanta, PhD Institute for Cardiovascular Prevention, Ludwig-Maximilians-University Bioelectronic Medicine 2020, 6(Suppl 1):S17.

Vagus nerve stimulation in Crohn's disease: A 12-month pilot study outcomes Bruno Bonaz, MD-PhD CHU and Grenoble Institute of Neurosciences (GIN)-INSERM Bioelectronic Medicine 2020, 6(Suppl 1):S18.

Electrical activation of neural reflexes for the treatment of autoimmune diseases David Chernoff, MD SetPoint Medical Bioelectronic Medicine 2020, 6(Suppl 1):S19.

The jump from animals to humans: How to make the jump easier Kip Ludwig, PhD University of Wisconsin Bioelectronic Medicine 2020, 6(Suppl 1):S20.

Bioelectronic medicines that look good ON you Doug Weber, PhD University of Pittsburgh Bioelectronic Medicine 2020, 6(Suppl 1):S21.Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.