Journal of Tropical Medicine

Volume 2014 (2014), Article ID 131835, 6 pages

http://dx.doi.org/10.1155/2014/131835

Research Article

Early Treatment with Intranasal Neostigmine Reduces Mortality in a Mouse Model of Naja naja (Indian Cobra) Envenomation

Matthew R. Lewin,¹ Stephen P. Samuel,² David S. Wexler,³ Philip Bickler,⁴ Sakthivel Vaiyapuri,⁵ and Brett D. Mensh⁶

¹Center for Exploration and Travel Health, California Academy of Sciences, 55 Music Concourse Drive, San Francisco, CA 94118, USA

²Department of Clinical Medicine, Trinity College Dublin, Dublin 2, Ireland

³Department of Chemistry and Biochemistry, University of California, Berkeley, Berkeley, CA 94920, USA

⁴Department of Anesthesia and Perioperative Care, 505 Parnassus Avenue, University of California, San Francisco, CA 94122, USA

⁵Institute for Cardiovascular and Metabolic Research, School of Biological Sciences, University of Reading, Reading, UK

⁶Janelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA

Received 1 April 2014; Revised 19 April 2014; Accepted 19 April 2014; Published 14 May 2014

Academic Editor: Marcel Tanner

Copyright © 2014 Matthew R. Lewin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Objective. Most snakebite deaths occur prior to hospital arrival; yet inexpensive, effective, and easy to administer out-of-hospital treatments do not exist. Acetylcholinesterase inhibitors can be therapeutic in neurotoxic envenomations when administered intravenously, but nasally delivered drugs could facilitate prehospital therapy for these patients. We tested the feasibility of this idea in experimentally envenomed mice. Methods. Mice received intraperitoneal injections of Naja naja venom 2.5 to 10 times the estimated LD50 and then received 5 μL neostigmine (0.5 mg/mL) or 5 μL normal saline by nasal administration. Animals were observed up to 12 hours and survivors were euthanized. Results. 100% of control mice died. Untreated mice injected with 2.5× LD50 Naja naja died at average 193 minutes after injection, while 10 of 15 (67%) of treated mice survived and were behaviorally normal by 6 hours (). In the 5× LD50 group, survival was prolonged from 45 minutes to 196 minutes () and for 10× LD50 mice, survival increased from 30 to 175 minutes (). Conclusion. This pilot suggests that intranasal drugs can improve survival and is the first direct demonstration that such an approach is plausible, suggesting means by which treatment could be initiated before reaching the hospital. Further investigation of this approach to neurotoxic and other types of envenomation is warranted.

1. Introduction

Bites from venomous snakes kill more people in the developing world than some of the world’s better recognized and better studied neglected tropical diseases [1]. Recent estimates suggest that worldwide there are more than 5 million snakebites occurring each year. Though not all bites are by venomous snakes or result in poisoning, up to 2 million of these bites result in the injection of venom, with hundreds of thousands of significant injuries and as many as 94,000 to 125,000 deaths occurring primarily in India, Southeast Asia, and sub-Saharan Africa [2, 3]. The vast majority of snakebites occur in impoverished, rural populations with limited access to medical treatment. Mortality from snakebite is unequivocally linked to socioeconomic markers of poverty and even a successful hospital treatment can cause economic ruin. A recent study from the Indian state Tamil Nadu analyzed how patients hospitalized for snakebite paid for their expenses: 40% took loans, 20% sold stored crops, 15% sold valuables 10% sold cattle, and many reported removing their children from school—all while incurring up to 12 years income worth of debt [2]. It is estimated that around 10,000 people die from snakebite each year in Tamil Nadu, alone [2], more than twice the total number of deaths claimed by landmines each year, worldwide [4, 5].

Neostigmine is an acetylcholinesterase inhibitor (AChEI) that is administered intravenously and is currently recommended by the WHO for the treatment of neurotoxic snakebite. Acetylcholinesterase inhibiting drugs such as neostigmine and edrophonium are thought to reduce the neuromuscular block from neurotoxic snakebite by increasing the amount of acetylcholine at the neuromuscular junction as it does in the treatment of myasthenia gravis or the reversal of nondepolarizing neuromuscular blocking agents [6–9]. Atropine or glycopyrrolate, in intravenous (IV) form, are usually coadministered with AChEIs to blunt the undesirable muscarinic effects of AChEIs. However, coadministration is not necessary in some clinical studies, for example, in myasthenia gravis patients receiving intranasal (IN) administration for up to one year [10, 11]. Interestingly, IN neostigmine has been used to treat myasthenia gravis in several studies [10–13] and we recently showed in a human study that it could reverse mivacurium-induced neuromuscular blockade by this route [14].

The present study tested the hypothesis that neostigmine, given IN, would be an effective initial treatment of Naja naja envenomed mice. The early use of AChEIs leads to a considerable increase in the LD50 in mice and rats having undergone experimental envenomation [15, 16]. Our study is distinguished from those by the replacement of parenteral neostigmine with topically applied IN neostigmine. The rationale for this study is that since neurotoxic snakebites often occur far from hospitals, by eliminating the need for injection (e.g., of parenteral neostigmine or intravenous antivenin), we may be able to shorten time to treatment and save lives.

2. Materials and Methods

2.1. Institutional

The study was approved by the animal research committee of a contract research laboratory in Hyderabad, India, an IACUC-certified laboratory and performed by a trained technician, a full-time DVM and one of us (MRL) who performed experiments at the facility.

2.2. Materials and Animals

Unfractionated N. naja venom was purchased from Sigma-Aldrich (St. Louis, MO, USA); neostigmine and atropine were purchased from Besse Medical (Ann Arbor, MI, USA). Venom and drugs were reconstituted in sterile water. Mice had access to water and food at all times. Polyvalent antivenom (Vins Bioproducts, Andhra Pradesh, India) was available at all times in the event of accidental envenoming of staff.

2.3. Methods

A small pilot study was carried out to assess the potency of the reconstituted lyophilized N. naja venom to test if it was comparable to published reports of other commercially available unfractionated, frozen, or lyophilized N. naja venom at 0.3 mg/kg [15, 17–19].

Mice were pseudorandomized in batches of 5 with tails marked 1 to 5 stripes by Sharpie felt tip pen to receive intraperitoneal (IP) injections of N. naja venom (2.5× LD50, ; 5× LD50, and 10× LD50, ) concomitantly with atropine, which blunts the muscarinic effects of neostigmine and has previously been shown to have no effect on LD50 when experimentally injected with snake venom [16]. The IP agents (venom and atropine) were adjusted for the weight of each individual mouse by the facility veterinarian and injected by a single technician who was not aware of the hypothesis and who also recorded the survival times. Animals received either 5 μL of 0.5 mg/mL neostigmine or 5 μL of saline by IN administration by MRL. Animals in the 2.5× LD50 group received treatment or control 10 minutes after venom injection. In the 5× LD50 and 10× LD50 groups, animals received IN neostigmine 1-2 minutes after venom injection. Preliminary studies the mice were already severely disabled by 10 minutes after experimental envenomation with the higher doses of venom and neostigmine did not appear to help. Animals were observed continuously for up to 12 hours and assessed for signs of toxicity including respiratory distress, loss of spontaneous locomotor activity with the only endpoints being time to death or recovery. Dead mice were removed immediately and tail-band number was recorded on a data sheet reflecting the mouse’s lot and individual band number as well as weight. Surviving animals were euthanized after 12 hours by the same technician who performed the experimental envenomation procedure. The technician, however, was blinded to knowing which mice had been treated with IN neostigmine or saline control.

2.4. Data Analysis and Presentation

Data were analyzed using GraphPad Prism (La Jolla, CA) and the values presented in the figures were as calculated by nonparametric Mann-Whitney test. Envenomed mice were further characterized using a survival analysis that included censoring to account for the study being terminated at 12 hours (720 minutes) after dosing. To plot survival time on a single -axis, the survival time data was normalized within each envenomation dose to the mean survival time of each control group and then multiplied by 100.

3. Results

Because snakebites in the community can result in a highly variable amount of venom being delivered to the patient, we sought to determine whether IN neostigmine could be effective in improving survival at several dosages of venom in our mouse model. There were no statistically significant differences in animal weight between any of the groups. Figures 1(a)–1(c) show the effects of neostigmine in mice envenomed with Naja naja venom at various concentrations: 2.5× LD50 (a), 5× LD50 (b), and 10× LD50 (c). As described above, the rationale for using IN neostigmine is to improve survival time from the moment of the snakebite. These results support our idea that early IN AChEI therapy could improve survival even after a potentially severe neurotoxic envenomation. Higher venom dosages resulted in earlier deaths, as expected, but for all dosages of venom, neostigmine provided a substantial and persistent window of increased survival. Table 1 summarizes the data from all groups. At 2.5× LD50, envenomed mice died at an average of 193 minutes compared to 553 minutes () for the treatment group (10/15 were euthanized after the arbitrary cutoff of 6 hours, but were behaving completely normally). At the 5× LD50 venom dosage, survival was prolonged from a mean of 45 minutes in the control group to 196 minutes in the treatment group (). Likewise, at the 10× LD50 venom dosage, mean survival was prolonged from 30 to 175 minutes (). Findings reached statistical significance even after reanalysis excluding surviving outliers in the 5× LD50 and 10× LD50 groups.

Table 1: Survival times for all venom dosages compared with and without IN neostigmine treatment. values shown were as calculated by nonparametric Mann-Whitney test.

Treatment
Mean survival time in minutes (range)
value
Number of mice per group

2.5× LD50 venom
193 (67–332)
<0.02
5

2.5× LD50 + neostigmine
553 (144–720)
15

5× LD50
45 (40–48)
=0.01
5

5× LD50 + neostigmine
196 (50–720)
5

10× LD50
30 (25–35)
<0.02
5

10× LD50 + neostigmine
175 (35–720)
5

(a)

(b)

(c)

Figure 1: Kaplan-Meier plot of survival times in mice given 2.5 (a), 5 (b), or 10 (c) times the LD50 of N. naja venom and either a single dose of IN neostigmine (treatment groups, blue lines) or IN saline (control groups, red lines). animals for each group, except for the 2.5× LD50 treatment group. There were no significant differences in the mean weight of animals across groups.

4. Limitations

Most bites in humans are on the extremities, but we chose the IP route for consistency and to replicate elements of previously published mouse studies [15–17]. Due to limitations of funding, we only tried one type of experimental envenomation using a curare-like snake neurotoxin; it is likely that the effects of IN AChEIs will vary across different venom types. Venoms contain a multitude of toxic peptides and proteins and published LD50 ranges vary widely between cobra species, subspecies and route of delivery (e.g., subcutaneous, intravenous, or IP) [15, 17–20]. Mice and humans differ greatly in their sensitivity to the same drugs [21, 22], and only one set of neostigmine to atropine concentrations was used. Thus, as with all transitions from preclinical to clinical usage, dosages will need to be optimized for human use. Fortunately, the development of IN neostigmine for the treatment of myasthenia gravis [10–13, 23, 24] provides a substantial head start for this transition. Only a single dose of IN neostigmine was administered, so it is not clear if mice would have survived longer with multiple treatments and no other AChEIs were tested. The concentration of neostigmine was significantly lower than that has been used in human studies, though total dose was comparable and the drugs were not aerosolized but dropped on the nares [10–14]. In the present study, atropine was coadministered with IN neostigmine through IP route. In previous mouse studies atropine has been administered IP without changing the LD50 of cobra venom [15]. We anticipate that an anticholinergic agent such as atropine (which can be administered IN) would potentially be administered with neostigmine to blunt untoward muscarinic effects of an AchEI should these effects be present with IN AChEI formulations in a human study [25]. Interestingly, in the year-long study by Sghirlanzoni and colleagues, patients self-administering IN neostigmine did not report any complications from IN neostigmine [11]. Broggini and colleagues tested the bioavailability of high dose IN neostigmine compared to IV administration in healthy human adults without coadministration of atropine and did not note any serious adverse events [23]. The IP-absorption kinetics of atropine are more reliable and proven than the IN absorption kinetics of atropine. Thus, if we had coadministered atropine IN instead of IP, we would be faced with the confoundedness that perhaps differential survival depended on intersubject differences in atropine-absorption kinetics. This confoundedness would be impossible to disambiguate from our central hypothesis in such a small study. By contrast, if survival depended on differential IN absorption kinetics (of neostigmine), that simply serves to further support the central hypothesis that neostigmine is the critical variable, especially in light of Gieu’s results showing that IP atropine did not materially alter survival from experimental IP cobra envenomation [15]. We did not do necropsy on the mice. Similarly, we did not attempt any skin hemorrhagic or myonecrosis activity assays, though no unusual bleeding was noted. Mice were only observed for neurological manifestations of envenomation such as convulsion, hind limb paralysis, and respiratory distress after injection of reconstituted venom [17].

5. Discussion

Muscle-contraction-dependent respiration is a necessary condition for life amongst all mammals and virtually all vertebrates. The present finding builds on our earlier demonstration that IN neostigmine could reverse paralysis in an awake, experimentally paralyzed human subject [14]. To our knowledge, this is the first demonstration that a topically applied drug could reverse venom-induced neurotoxicity. We previously showed that nasal neostigmine could reverse mivacurium-induced paralysis in an awake human [14]. Together, these data provide proof-of-principle that venom-induced toxicity should be treatable in the out-of-hospital setting and provide early, life-saving interventions at low cost. There is evidence for neostigmine-resistant envenomings [26] in humans. Anil and colleagues showed that the mean time interval between bite and arrival to hospital was 4.5 h by which point the venom would have been entrenched at presynaptic axons [26]. Rapid death from krait bite most often comes as a result of the alpha-toxin and diaphragmatic paralysis and airway obstruction could be delayed by early AChEI therapy, but to our knowledge this idea has never been tested. In mouse studies, Guieu showed that among the drugs they tested only AChEIs consistently resulted in increases in Naja venom LD50s while atropine had no effect on the LD50 [15]. Similarly, Flachsenberger [16] showed that at otherwise lethal doses, all animals survived as a result of early AChEI treatment following IP administration of adder (Acanthophis antarcticus) venom. Flaschenberger further found that the expected survival time of animals subjected to even higher experimental venom doses was significantly extended. These animal [15, 16] and human morbidity and mortality studies suggest that if AChEIs can be administered during the initial, critical stage after envenomation there could be a survival benefit to human victims [16, 27–32].

Surprisingly, both the efficacy and optimal uses of antivenom and AChEI therapies for neurotoxic snakebite remain unproven even after decades of widespread use [2, 14, 33–38]. It has been argued that the development of more diverse and regionally specific antivenoms is the most cost effective means of combatting morbidity and mortality from snakebite in the developing world [39–41]. We argue that investment in repurposed, low-molecular-weight pharmaceuticals would be more cost effective in the long term because of their ease of use, heat stability, and safety profiles. IN administration of neostigmine has the potential to provide snakebite victims with significantly increased access to an effective treatment for neurotoxic snakebite while suggesting a strategy for the development of topically administered antidotes to hemotoxic, cardiotoxic, and other complex envenomation in the future. This type of innovation would save lives while significantly lowering the economic burden on individuals, families, communities, and governments. To date, no prospective human study has been done to analyze the effect of immediate AChEI administration in the setting of neurotoxic snakebite. The primary aim of this pilot study was to test if early IN administration of AChEIs and in principal any venom-inhibiting agent is plausible. The results of this study suggest that this is the case and that significant further study of this and other strategies is warranted.

Conflict of Interests

Matthew R. Lewin filed a provisional patent PCT/US2013/058640. Stephen P. Samuel, David S. Wexler, Philip Bickler, Sakthivel Vaiyapuri, and Brett D. Mensh have no conflict of interests.

Authors’ Contribution

Matthew R. Lewin carried out paper outlining, experimental design, and experiments; Stephen P. Samuel carried out paper outlining, experimental design, and preparation; David S. Wexler carried out paper outlining, experimental design, and data analysis; Philip Bickler carried out paper outlining; Sakthivel Vaiyapuri carried out paper outlining, data analysis, and figures; Brett D. Mensh carried out paper outlining, data analysis, and interpretation. Stephen P. Samuel and Matthew R. Lewin contributed equally to the production of this paper.

Funding

Unrestricted funds were provided from California Academy of Sciences Center for Exploration and Travel Health Snakebite Research Project.

Acknowledgments

This paper is dedicated to Dr. Susan Lewin and the authors also thank Mr. Jerry Harrison, Dr. David Lewin, Drusilla Davis, TCR Multispecialty Hospital (Krishnagiri, Tamil Nadu, India), and Anita and Sunita Rao for their timely logistic support.

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