key: cord-0746511-m0ct29rp
authors: Clark, Nicole F.; Taylor-Robinson, Andrew W.
title: COVID-19 Therapy: Could a Chlorophyll Derivative Promote Cellular Accumulation of Zn(2+) Ions to Inhibit SARS-CoV-2 RNA Synthesis?
date: 2020-08-14
journal: Front Plant Sci
DOI: 10.3389/fpls.2020.01270
sha: b1018cb523136a2681d88bf653c094736c69dc6b
doc_id: 746511
cord_uid: m0ct29rp

nan

cell lines, the most commonly used in vitro model to represent the alveoli of the lungs, a broad array of cell types has been shown to respond to ZnPh (Jakubowska et al., 2013; Ocakoglu et al., 2015) . Zn 2+ ions attached to this tetrapyrrole derivative can pass through cell membranes as it is water-soluble. Aggregation and accumulation by different organelles of pheophorbide a and other chlorophyll breakdown products, both with and without Zn 2+ , are demonstrated in many studies (Tao et al., 1990; Szczygieł et al., 2008; Yoon et al., 2011; Ahn et al., 2012; Tamiaki et al., 2012; Xodo et al., 2012; Jakubowska et al., 2013; Ocakoglu et al., 2015; Ahn et al., 2017; Kang et al., 2018; Mokwena et al., 2018; Singh et al., 2019; Zhou et al., 2019; Tamiaki et al., 2020) . Interestingly, no localization of ZnPh to mitochondria has been observed (Jakubowska et al., 2013; Ocakoglu et al., 2015) . Therefore, ZnPh is unlikely to impair the function of mitochondria in healthy cells, highlighting a number of potential benefits to this treatment. Moreover, since the charge separation of Cu 2+ and Zn 2+ ions is identical, with the latter displaying only a slightly higher electronegativity, ion substitution of pheophorbides with Zn 2+ aids the solubility of ZnPh. Hence, this improves the ability of ZnPh to be a carrier molecule for the free ionisation of Zn 2+ (Ferruzzi and Blakeslee, 2007; Jakubowska et al., 2013; Ocakoglu et al., 2015; Martinez De Pinillos Bayona et al., 2017; Kang et al., 2018) and thus potentially to act as a drug delivery system.

It has been suggested that as a clinical treatment, ZnPh may be used in conjunction with photodynamic therapy (ultraviolet B irradiation) to induce singlet oxygen stress and ionisation of Zn 2+ molecules, resulting in cytotoxicity towards carcinogenic cells lining the human lungs (Jakubowska et al., 2013) . There is also a low overall cytotoxic effect in murine models, with animals generally healthy throughout treatment indicative of limited systemic side effects (Jakubowska et al., 2013; Ocakoglu et al., 2015) . As with nonmetallated organic molecules, above a threshold concentration ZnPh, is cytotoxic in the dark, a phenomenon that continues upon illumination; however, at low concentrations, no cytotoxic effect is observed regardless of the level of light intensity (Jakubowska et al., 2013; Ocakoglu et al., 2015) . Exposure and singlet oxygen stress can be controlled according to light spectrum settings, i.e. red light versus blue light. Whether irradiated or not, light-induced cytotoxicity that is triggered by pheophorbides is dose-related and diminishes rapidly (Ahn et al., 2012; Jakubowska et al., 2013; Ocakoglu et al., 2015) , and no systemic toxicity has been detected (Ahn et al., 2017) .

ZnPh and similar non-metallated forms facilitate the successful transmembrane passage of non-polar components of a molecule, wherein irradiance alters the ionic concentration offree ions once it has entered into the cytoplasm (Martinez De Pinillos Bayona et al., 2017) . Free Zn 2+ appears to promote an antiviral effect, research in vitro demonstrating accumulation of Zn 2+ in human lung tissue (Hagimori et al., 2019) . Moreover, increasing the cellular concentration of Zn 2+ through zinc supplementation and using ionophores such as pyrithione efficiently impairs RNA replication by human coronaviruses, leading to improved treatment outcomes (te Velthuis et al., 2010; Read et al., 2019; Derwand and Scholz, 2020; Zhang and Liu, 2020) . Similarly, sucking zinc lozenges reduces symptoms of viral respiratory infection (Turner and Cetnarowski, 2000) . Zinc ionophores are effective at increasing concentrations of Zn 2+ because they allow more zinc to pass through the cell membrane (Zhang and Liu, 2020 ). Yet, as uptake of zinc is a less efficient and therefore slower metabolic process in eukaryotes (Kręzėl and Maret, 2006) , very little is known about zinc ionophores as transporters (Gaither and Eide, 2001) .

The primary function of an ionophore is to increase cell permeability to enable transport of ionic compounds across the cell membrane by endocytosis. Although this is a role fundamental to normal functioning of a healthy cell, the presence of ionophores can weaken the integrity of the cell membrane, thus paradoxically leading to decreased cell defence systems (Gaither and Eide, 2001; te Velthuis et al., 2010; Derwand and Scholz, 2020) . However, it is not known if ZnPh also weakens cell membranes nor whether the rate and/or extent of ionisation of free zinc is increased during this uptake. Despite ZnPh not being a recognized ionophore, as it is highly soluble when irradiated, uptake of Zn 2+ is likely to be improved by this process (Szczygieł et al., 2008; Tamiaki et al., 2012; Martinez De Pinillos Bayona et al., 2017; Hagimori et al., 2019) . Studies using in vitro cultured cells point to the capacity of ZnPh to elevate free ion concentrations of Zn 2+ (Jakubowska et al., 2013; Ocakoglu et al., 2015) . If this effect translates successfully from in vitro to in vivo, then such a mechanism would reduce the therapeutic demand for the use of toxic or dose-dependent ionophores such as hydroxychloroquine.

While our understanding of the metabolic processes of zinc transporters remains limited, it is plausible to speculate that ZnPh combined with zinc supplementation could reach deep inside human lungs (Jakubowska et al., 2013) . This would increase the cellular concentration of Zn 2+ to target cells such as alveolar epithelia (Hagimori et al., 2019) , corroborating in vitro studies on the free ionisation of Zn 2+ (Szczygieł et al., 2008; Tamiaki et al., 2012; Hagimori et al., 2019; Zhou et al., 2019) . Additionally, such raised intracellular levels may be achieved independently of the need for a cytotoxic effect experienced both in the dark and upon illumination, eliminating associated risks of singlet oxygen stress, ionisation and phosphorylated nuclear cell damage. Therefore, since ZnPh is water-soluble, it is reasonable to consider that ionic uptake of Zn 2+ is increased, potentially producing a similar effect as observed with other ionophores such as pyrithione and hydroxychloroquine (Derwand and Scholz, 2020) . Together with zinc supplementation, this may significantly impair replication of human coronaviruses, notably SARS-CoV-2, under experimental conditions. Hence, we propose that this novel therapy merits further evaluation to develop long-term as a possible clinical treatment of symptomatic COVID-19 patients.

The drug delivery capacity of chlorophyll derivatives depends on the properties of each compound (Ulbricht et al., 2014; Kang et al., 2018) , as some display non-polar behaviour in a dosedependent ratio (Jakubowska et al., 2013; Ocakoglu et al., 2015; Martinez De Pinillos Bayona et al., 2017) , thus emphasising the need for clinical trials (Tang et al., 2006; Ferruzzi and Blakeslee, 2007; Mishra et al., 2011; Ulbricht et al., 2014; Solymosi and Mysliwa-Kurdziel, 2017) . It is important to appreciate that replacement of the central ion in pheophorbides can yield varied results in vitro and in vivo, with some studies suggesting that ionic inclusion may reduce toxicity (Szczygieł et al., 2008; Tamiaki et al., 2012; Martinez De Pinillos Bayona et al., 2017; Tamiaki et al., 2020) . Accidental ingestion of non-dietary levels of pheophorbide a, a compound that lacks a central ion, induces a rare but mild phototoxic effect at low doses; however, this was still deemed safe for human consumption (Hwang et al., 2005) .

Chlorophyll is generally considered not harmful to humans (Ulbricht et al., 2014) , but information is scarce on any possible toxicity posed by chlorophyll derivatives, especially those compounds, both with and without ion inclusion, e.g. Zn 2+ , which have not been subject to clinical trials. Pre-clinical and clinical safety tests on ZnPh are required. However, it is generally accepted that toxicity is dependent on a photo-reactive response (Tao et al., 1990; Hwang et al., 2005; Szczygieł et al., 2008; Tamiaki et al., 2012; Jakubowska et al., 2013; Ocakoglu et al., 2015; Martinez De Pinillos Bayona et al., 2017; Zhou et al., 2019; Tamiaki et al., 2020) , given that phototoxicity induced by ZnPh is short-lived (Ahn et al., 2012; Jakubowska et al., 2013; Ocakoglu et al., 2015; Solymosi and Mysliwa-Kurdziel, 2017) . Rapid clearance of zinc chlorophyll compounds is observed in human cell lines, with low doses invoking no or limited cytotoxic effect (Tao et al., 1990; Tang et al., 2006; Jakubowska et al., 2013; Ocakoglu et al., 2015; Martinez De Pinillos Bayona et al., 2017; Diogo et al., 2018) .

Here, we provide an insight into the properties of ZnPh that make this chlorophyll derivative a potential therapeutic agent for treating COVID-19. Our understanding of ZnPh and similar compounds relates to the reported success of in vitro and in vivo cancer studies, so this recognised drug delivery system has not been used yet as a treatment for respiratory illness. However, the possibility that this may translate to an anti-viral property merits investigation.

Unless a pronounced phototoxic effect is inducedhighly unlikely under physiological conditions -ZnPh is non-toxic to humans. Therefore, there is a strong likelihood that this compound offers great potential to act as a carrier molecule for Zn 2+ to trigger an anti-viral response that impairs SARS-CoV-2 replication. Hence, Zn 2+ ionophores provide a novel therapeutic option that may be of benefit to the development of an effective treatment for the severe clinical manifestations of COVID-19.

Both authors (NC and AT-R) made substantial contributions to the conception of the work and to literature search, contributed significantly to writing the manuscript, revised it critically for important intellectual content, approved its final version and agreed to its submission.

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