key: cord-1015109-gkj8c1f7
authors: de Gurtubay, Iñaki Garcia; Bermejo, Pedro; Lopez, Miguel; Larraya, Iñaki; Librero, Julian
title: Evaluation of different vagus nerve stimulation anatomical targets in the ear by vagus evoked potential responses
date: 2021-09-22
journal: Brain Behav
DOI: 10.1002/brb3.2343
sha: dbfb388e414b194b410b7104e0e8fe4a27f39ead
doc_id: 1015109
cord_uid: gkj8c1f7

BACKGROUND: Electrical auricular vagus nerve stimulation (taVNS) is an emerging therapy. Stimuli are transported to brainstem nuclei, whereby its multiple projections reach to many subcortical and cortical areas, thus allowing the neuromodulation of several systemic physiological processes. We aim to define the best auricular target for taVNS through vagus somatosensory evoked potential (VSEP) elicited stimulating different auricular areas with different electrode sizes. METHODS: Twenty‐six subjects were enrolled. Three stimulation areas were studied: simultaneous cymba and cavum (CC), cymba (C) and earlobe (L); and two electrode sizes: extra‐large (X) and small (S). We studied the effect of five combinations (CCX, CCS, CS, LX and LS) on VSEP´s latency and amplitude, and sensory and pain threshold (Pt) using a lineal mixed model regression analysis. We used CS combination, used in a commercial device, as reference model. RESULTS: Valid VSEP were obtained for CCX, CCS and CS but not in LX and LS. Both CCS and CCX tests showed significant amplitude increases. The same effect was observed in CCX using CCS as reference. Significant increases in Pt were found for CCX and LX. The same effect was observed in CCX using LX as reference. CONCLUSION: The results suggest that CC and C areas are active targets for taVNS but not for earlobe, as anatomical data support. Considering that amplitude reflects the synchronized electrical activity generated, we conclude the most effective topography is the simultaneous stimulation of cymba and concha. The use of X‐sized electrodes increases the amplitudes and makes the stimulation more comfortable.

The vagus nerve (VN) is the longest cranial nerve and is involved in the regulation of multiple systems (H. Yuan & Silberstein, 2016) . Therefore, due to this influence on multiple systems and its important role in maintaining homeostasis, stimulating this nerve to modulate the function of related organs has long drawn the attention of investigators (T.-F. .

As a slow-acting therapy, cervical vagus nerve stimulation (VNS) has been approved by the US Food and Drug Administration for managing treatment refractory epilepsy in 1997 and for chronic treatmentresistant depression in 2005 (H. Yuan & Silberstein, 2016) . However, surgical risks, technical challenges and potential side effects have limited the application of VNS (Fitzgerald, 2013; Ventureyra, 2000) .

To overcome such barriers of applying invasive VNS (iVNS), some noninvasive transcutaneous vagus nerve stimulation (tVNS) methods have been developed, superficially stimulating the VN at the neck or at the outer ear.

The rationale of tVNS on the ear is based on anatomical studies demonstrating that certain parts of the ear area have afferent VN distribution (Henry, 2002; Peuker & Filler, 2002; Trevizol et al., 2015) , and electrical stimulation of these areas may produce activity changes in the VN pathway in the brain stem and central structures (Shiozawa et al., 2014) , producing a modulation effect similar to iVNS (Carreno & Frazer, 2016; Hein et al., 2013 ; P.-J. Rong et al., 2012) . The auricular branch of the vagus nerve (ABVN) spans from the main bundle of the VN and innervates the external ear (Berthoud & Neuhuber, 2000; Dabiri et al., 2020) , although its afferent projections are still not well understood. It is known that the cymba conchae of the external ear is innervated exclusively by this branch, but other regions of the external ear receive important afferent innervation by ABVN solely (Peuker & Filler, 2002) or shared with other nerves such as the tragus, the posterior and inferior walls of the ear canal (Fay, 1927; Tekdemir et al., 1998) and the cavity of the conchae (Berthoud & Neuhuber, 2000) . So, using ABVN as target of noninvasive brain stimulation is known as transcutaneous auricular vagus nerve stimulation (taVNS).

taVNS has been used to treat disorders, such as epilepsy (P. Rong et al., 2014; Stefan et al., 2012) , prediabetes , depression (H. Yuan & Silberstein, 2016) , chronic tinnitus (Shim et al., 2015) , migraine , rehabilitation after ischemic stroke (Baig et al., 2019) , ventricular arrhythmias (Nasi-Er et al., 2019), respiratory symptoms associated to COVID-19 (Staats et al., 2020) as well as to boost associative memory (Jacobs et al., 2015) what has been proposed to help patients with Alzheimer's disease and other dementia types (Cai et al., 2019; Kaczmarczyk et al., 2017) .

Those clinical effects depend on various parameters of the taVNS such as the electrode position, stimulus duration, interstimulus interval and the stimulus intensity (Hagen et al., 2014) . However, currently different stimulation targets and parameters are used, which make it difficult to evaluate and compare the potential therapeutic applications.

Investigators have recently focused the discussion on which anatomical target is most biologically active. The vagally innervated region of the ear is usually selected to stimulate according to sparse and limited human auricle dissection anatomical studies (Bermejo et al., 2017; Oken, 1997) (Ay et al., 2015; Suk et al., 2018) , the tragus (Badran et al., 2018) , the external auditory channel or some of its specific parts (Skraus et al., 2013) . . This nuclear region of the vagus nerve has multiple projections to many subcortical and cortical brain regions, which explain the long-distance physiological modulation of vagus stimulation. The postsynaptic brainstem activity from the VN nuclei can be recorded at the scalp as far field potential (Fallgatter et al., 2003; Polak et al., 2009; Usami et al., 2013) called vagus somatosensory evoked potential (VSEP) and is only elicited when stimulating within the innervation area of the ABVN, while no evoked potential will be recorded stimulating at other sites. The characteristics of this VSEP have been described in normal population (Fallgatter et al., 2003; Lewine et al., 2019; Polak et al., 2009 ) as well as pathological conditions (Polak et al., 2017 (Polak et al., , 2013 (Polak et al., , 2011 (Polak et al., , 2007 (Polak et al., , 2014 . On the other hand, VSEP obtained by taVNS are like those seen with invasive VNS (Nonis et al., 2017) .

The amplitude of an evoked potential mainly reflects the amount of electric potentials generated along the stimulated neural pathway as a representation of the amount of stimulated neural fibers. So, the aim of our study was to define the best auricular target for taVNS comparing the characteristics of VSEP elicited when stimulating over three different auricular sites with two electrode sizes and to define the optimal combination that evokes higher amplitude VSEP. As secondary objective, we wanted to find optimal stimulation intensity ranges, sufficient and acceptable to generate VSEP but not reaching to be painful, that could be used for prolonged in time taVNS clinical studies.

A total of 26 healthy volunteers participated in the present study, approved by the ethics committee of our centre. Written informed consent was obtained from all participants. The exclusion criteria were

(1) intake of any medication, (2) history of neurosurgical treatment,

(3) ear lesions or infections, (4) allergy to Ag/AgCl, (5) pregnancy or breastfeeding, (6) history of neuropathy (including autonomic or diabetic neuropathy) and (7) history of traumatic brain injury. Ag/AgCL electrode that we call extra-large electrode (X). To obtain the small electrode (S), we cut and reduced the surface of X electrode to 2.3 × 2.3 mm (5.3 mm 2 ). The size of S electrode was chosen to be similar to the stimulation surface used by the NEMOS-Cerbomed device, one of the most widely used commercial taVNS systems (Burger et al., 2018; Frangos et al., 2015) .

We selected three different stimulation topographies, all of them in the left ear: cymba and cavum (CC) with cathode in cymba and anode in cavum conchae, cymba (C) with cathode and anode with 3 mm interelectrode distance; and lobe (L) with both electrodes over the ear lobe.

We cleaned the ear with alcohol, dried it and used Collodion SLE-UK medical adhesive to attach stimulating electrodes over these areas. So, from the combination of three topographies and two electrode sizes, we conducted five different experimental paradigms called tests to our volunteers in a single afternoon session: CCX, CCS, CS, LX and LS. CX test was not done because there was not enough space to attach X size electrode over the cymba (Figure 1 ). Electrical brain activity was recorded and data were processed with a commercial EMG and evoked potential system (Synergy Viasys HealthCare) and software V.15.0).

We used the same electrical stimulation parameters for the five tests, with electrical 500 μs square impulses of alternating polarity and 1 Hz frequency. At the beginning of each test, the sensory threshold (St) was measured with a progressive increase of stimulation intensity from 0 mA to that at which the subject began to perceive the stimuli. Then, we also measured the pain threshold (Pt), the lowest intensity at which stimuli were perceived as painful. To avoid stimulation of other nerve fibers or artefact responses, we never stimulated over 5 mA.

For each subject, the first test was always CS, and the remaining tests were randomly assigned. After measuring St and Pt in CS condition, we calculated the stimulus intensity value that we used to elicit the VSEP increasing by 2.5 the St value. We fixed this intensity also for the remaining test regardless their specific St value. Then, we asked volunteers to relax themselves and to close their eyes and we began the test.

VSEP were recorded over the F3-C3 bipolar derivation (Hagen et al., 2014) . To avoid contaminated responses and consider a VSEP as valid, at least 50 consecutive artifact free signals must be averaged with the automatic artifact rejection system at ±30 μV. When we obtained at least two stable and consistent valid VSEP, we continued to the next test. The parameters of the VSEP manually measured for every condition were latency to the VSEP onset, onset to peak amplitude and duration. The experimenters evaluating the study outcomes were blinded to the order of the stimulation parameters.

We proceeded to investigate the effect of different topography and size combination on latency, amplitude, sensory threshold and pain threshold, using a lineal mixed model regression analysis with topography and size as fixed effects and individuals as random intercept. The intercept is the mean for the reference group (CS combination). We choose a sample size that allows to process it as normally distributed (Oken, 1997) . All data were preprocessed and statistically analyzed using the R software package Ime4.

The timing of the procedure for any test was as follow: 5 min to prepare skin, reduce and measure impedances, fix stimulating 

No statistical differences were found between the latencies of our reference test (CS) and CCS (p = .303) or CCX (p = .094) tests (Table 1a) .

When analyzing the amplitudes of the VSEP and using CS combination as reference values for them, we found significant (p < .001) increases To avoid the influence of topography, we reanalyzed and using CCS data as reference we compared CCX test amplitudes (Table 1b) . We found significant increases (p < .001) in the amplitudes 1.18 (CI 95% 1.05-1.31) for this last test (Table 1b) .

Compared to the CS combination, the sensory threshold for CCS did not produce any significant differences (p = .567). The slightly higher mean threshold values obtained for remaining tests were significant for LS (p = .045), CCX (p < .001) and LX (p < .001) as shown in Table 1a .

Compared to the CS combination, the pain threshold for the tests using S size electrodes were not significant (p = .597 for CCS and p = .068

for LS). However, the increases of Pt registered for CCX 0.86 (CI 95% 0.70-1.03) and for LX 0.54 (CI 95% 0.37-0.70) resulted both significantly higher (p < .001) as shown in Table 1a .

Comparing with LX test, we found that the Pt increases in CCX test 0.33 (CI 95% 0.16-0.49) were significant (p < .001) as shown in Table 1c .

To the best of our knowledge, this is the first study comparing the classical cymba conchae stimulation and the cavum and cymba conchae simultaneous stimulation. Our findings reveal that stimulation over C and CC topographies in healthy adults produces clear and reproducible evoked potential with latency and morphology close to those described previously as VSEP (Fallgatter et al., 2003) which reflects far field potentials of postsynaptic brainstem activity from the VN nuclei that can be elicited on electrical stimulation of the ABVN (Fallgatter et al., 2003; Polak et al., 2009) . In contrast, these evoked potentials are not registered when we stimulate over the earlobe. This suggests that stimulating over C and CC topographies activates vagus pathway but it is not activated when stimulating over the earlobe.

Assuming that the amplitude of an EP reflects the amount of synchronized electrical activity generated as a consequence of the stimulation, as we systematically obtained significant higher responses on CC topography, being independent of which electrode size has been used to stimulate, we could conclude that the stimulation of the ABVN is also higher. This suggests that cavum is a likely biologically active target, able to stimulate the ABVN and to enhance the classically used cymba conchae stimulation. On the other hand, our finding points that the earlobe is not an active target, at least with respect to ABVN stimulation.

Anatomical data support the use of these two locations, cymba and cavum conchae, for taVNS. Cymba conchae has clearly a large number of VN fiber endings with 100% of ABVN nerve supply (Peuker & Filler, 2002) , and its stimulation has demonstrated to produce significant activation of the classical central vagal nerve projections, for example, widespread activity in the ipsilateral NTS, bilateral spinal trigeminal nucleus, dorsal raphe, locus coeruleus, contralateral parabrachial area, amygdala and nucleus accumbens (Badran et al., 2017; Frangos et al., 2015; Yakunina et al., 2017) . Some medical devices (e.g., NEMOS, Cerbomed GmbH) have been commercialized to stimulate this area and treat different neurological and psychiatric disorders. On the other hand, an important VN innervation of cavum conchae and external auditory channel has been recently described by our group (Bermejo et al., 2017) with a variable percentage of myelinated nerve fibers, therefore able to be activated by transcutaneous stimulation.

These results are supported by other previous anatomical data (Ellrich, 2019; Safi et al., 2016 ) that demonstrate the existence and quantity of thick-myelinated afferent nerve fibers of the left auricular branch of the VN that carries a variable percentage of thick-myelinated afferent nerve fibers counted in the left thoracic VN in humans. So, that is why cavum has already been considered as a potential target to be used in taVNS therapies. Suk et al. (2018) suggested that isolated stimulation of cavum was more effective than cymba stimulation for the treatment of tinnitus. Ay et al. (2015) proposed the stimulation of this structure as a target for the protection of ischemic stroke in rats.

Most of these cavum and cymba conchae stimuli are driven by ABVN (He et al., 2013) , forming the so-called auriculo-vagal pathway (Ginsberg & Eicher, 2000) , but other nerves involved in the afferent innervation of the auricular area drive afferent signals of different nature to NTS. In fact, with regard to the anatomical perspective, the cavum is innervated by both the ABVN and the greater auricular nerve (GAN)

with 45% and 55% nerve supply, respectively (Peuker & Filler, 2002) . (Ginsberg & Eicher, 2000) . As registered evoked potential reflects the postsynaptic brainstem activity originated in NTS, we cannot discard some influence of the stimulated GAN fiber of cavum on the VSEP results, but we believe that is unlikely. Such an indirect long neural pathway would arrive later than direct afferents to NTS, producing a temporal dispersion of the VSEP and consequently a reduction in its amplitude. On the other hand, the ear lobule, which has been frequently used as a sham stimulation site in many taVNS studies, is innervated by GAN alone and does not generate VSEP at all. So, the anatomical distribution supports our results of obtaining an objective and measurable VSEP response when stimulating over C or CC areas, as a result of well synchronized postsynaptic potentials from jugular ganglion and NTS, but not over the earlobe. Usami et al., 2013; Yakunina et al., 2017) or even extra-auricular (Deuchars et al., 2018) nerves in addition to the VN.

With respect to stimulating electrode size and for a given stimulation strength of St x2.5 mA, our experiment showed greater VSEP amplitudes when using X size electrodes compared to smaller ones, being independent of which topography has been stimulated, suggesting a better recruitment of ABVN fibers close to the stimulation area.

Moreover, the tests that used X size electrodes systematically showed higher Pt over the same topographic targets, allowing the distribution of the electrical charge over a greater surface, and decreasing the intensity of the charge. Using greater electrodes over confirmed topographic targets allows to improve the stimulation efficiency to reach adequate therapeutic effects with lower intensities, specially avoiding the over-stimulation, and at the same time being more com- To sum up, we can conclude that from the tested combinations, we have identified two easily optimizable parameters for taVNS devices that elicit higher VSEP. On the one hand, performing a simultaneous stimulation over cymba and cavum regions of the ear would produce better response than cymba conchae stimulation alone. On the other hand, the use of X-sized electrodes improves vagus pathway activation and makes more comfortable the perception of the electrical stimuli. Both hypothetically could be related with a more intense clinical response and should be addressed in clinical trials.

All data generated or analyzed during this study are included in this published article.

The peer review history for this article is available at https://publons. 

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