Abstract
We investigated the cardiovascular effects of venoms from seven medically important species of snakes: Australian Eastern Brown snake (Pseudonaja textilis), Sri Lankan Russell’s viper (Daboia russelii), Javanese Russell’s viper (D. siamensis), Gaboon viper (Bitis gabonica), Uracoan rattlesnake (Crotalus vegrandis), Carpet viper (Echis ocellatus) and Puff adder (Bitis arietans), and identified two distinct patterns of effects: i.e. rapid cardiovascular collapse and prolonged hypotension. P. textilis (5 µg/kg, i.v.) and E. ocellatus (50 µg/kg, i.v.) venoms induced rapid (i.e. within 2 min) cardiovascular collapse in anaesthetised rats. P. textilis (20 mg/kg, i.m.) caused collapse within 10 min. D. russelii (100 µg/kg, i.v.) and D. siamensis (100 µg/kg, i.v.) venoms caused ‘prolonged hypotension’, characterised by a persistent decrease in blood pressure with recovery. D. russelii venom (50 mg/kg and 100 mg/kg, i.m.) also caused prolonged hypotension. A priming dose of P. textilis venom (2 µg/kg, i.v.) prevented collapse by E. ocellatus venom (50 µg/kg, i.v.), but had no significant effect on subsequent addition of D. russelii venom (1 mg/kg, i.v). Two priming doses (1 µg/kg, i.v.) of E. ocellatus venom prevented collapse by E. ocellatus venom (50 µg/kg, i.v.). B. gabonica, C. vegrandis and B. arietans (all at 200 µg/kg, i.v.) induced mild transient hypotension. Artificial respiration prevented D. russelii venom induced prolonged hypotension but not rapid cardiovascular collapse from E. ocellatus venom. D. russelii venom (0.001–1 μg/ml) caused concentration-dependent relaxation (EC50 = 82.2 ± 15.3 ng/ml, Rmax = 91 ± 1%) in pre-contracted mesenteric arteries. In contrast, E. ocellatus venom (1 µg/ml) only produced a maximum relaxant effect of 27 ± 14%, suggesting that rapid cardiovascular collapse is unlikely to be due to peripheral vasodilation. The prevention of rapid cardiovascular collapse, by ‘priming’ doses of venom, supports a role for depletable endogenous mediators in this phenomenon.
Similar content being viewed by others
Introduction
Snake venoms act as a defence against predators, aid in the capture and paralysis of prey, and assist in the digestion of prey1. They contain a multitude of toxins with a wide range of activities that target vital physiological processes. Many of the toxins responsible for the clinical manifestations of envenoming in humans have been extensively studied and pharmacologically/biochemically characterised. These venom components include neurotoxins2,3,4, myotoxins5,6,7, and components with pro-coagulant, anticoagulant, haemolytic and local tissue necrotic activity8,9,10. However, the nature and activity of the toxins affecting the cardiovascular system are less well understood.
There are a number of cardiovascular effects associated with snake envenoming, including hypotension, myocardial infarction, cardiac arrest, hypertension, brady- or tachy-cardia and atrial fibrillation10,11,12,13. Identifying the mechanism(s) responsible for venom-induced cardiovascular collapse has garnered more interest in recent years. We have previously defined ‘cardiovascular collapse’ as a sudden drop in recordable blood pressure14 following the administration of venom, to a laboratory animal or after human envenoming. The most common snakes responsible for this phenomenon are the brown snakes (Pseudonaja spp.)15 and, less commonly, taipans (Oxyuranus spp.)14 and tiger snakes (Notechis spp.)16. In some cases, patients spontaneously recover after collapse or respond well to basic and advanced life support17,18. In some cases of envenoming, particularly by brown snakes (Pseudonaja spp.), the collapse can be fatal16,17. Indeed, in Australia, cardiovascular collapse is the leading cause of death due to snake envenoming19.
A number of hypotheses have been proposed to explain the cause of the cardiovascular collapse associated with snake envenoming. Previous studies have postulated that cardiovascular collapse may be due to prothrombin activators or pro-coagulant toxins present in snake venoms20,21. We have recently demonstrated that in vivo cardiovascular collapse can be caused by death adder (Acanthophis rugosus) venom, despite a lack of pro-coagulants in this venom. This suggests that pro-coagulant toxins are not required to induce collapse15. Furthermore, administering small ‘priming’ doses of A. rugosus venom, prior to P. textilis venom, prevented subsequent cardiovascular collapse. This indicated that the release of depletable endogenous mediators most likely contribute to cardiovascular collapse. We also showed that the protective effect of priming doses of venom is transient (i.e. lasting up to approximately 1 hour), indicating replenishment of mediators15. This suggests that clotting factors are not directly involved in cardiovascular collapse, given the longer time period required for their resynthesis. Commercial polyvalent antivenom demonstrated a protective effect on cardiovascular collapse in vivo, supporting a role for antigenic venom components in cardiovascular collapse15.
To further investigate this phenomenon, in the present study we examined the cardiovascular activity of seven medically important snake venoms: Australian Eastern Brown snake (Pseudonaja textilis), Sri Lankan Russell’s viper (Daboia russelii), Javanese Russell’s viper (D. siamensis), Gaboon viper (Bitis gabonica), Uracoan rattlesnake (Crotalus vegrandis), Carpet viper (Echis ocellatus) and Puff adder (Bitis arietans). We identified the species which caused cardiovascular collapse in vivo to further investigate the possible mechanisms for this phenomenon.
Results
In vivo experiments
For these experiments 200 µg/kg (i.v.) was chosen as a standard dose for all venoms, unless a lower dose caused a similar response (i.e. D. siamensis 100 µg/kg, i.v.; E. ocellatus 50 µg/kg, i.v.; P. textilis 5 µg/kg, i.v.).
The mean blood pressure and heart rate of rats prior to administration of venoms were 97 ± 16 mmHg and 255 ± 63 b.p.m., respectively.
B. gabonica (200 µg/kg, i.v.), B. arietans (200 µg/kg, i.v.), C. vegrandis (200 µg/kg, i.v.) and D. siamensis (100 µg/kg, i.v.) venoms caused relatively minor hypotensive responses (i.e. between 11 to 35% decrease) in anaesthetised rats (Table 1). D. russelii (100 µg/kg, i.v) caused prolonged hypotension (45 ± 8% decrease) (Table 1). P. textilis (5 µg/kg, i.v.) and E. ocellatus (50 µg/kg, i.v.) venoms induced rapid cardiovascular collapse within 2 min of venom administration (Fig. 1a; Table 1).
To investigate the effects of artificial respiratory support, a higher dose of D. russelii venom (1 mg/kg, i.v.) was used, which caused a 100% decrease in blood pressure. This hypotensive effect (i.e. 100%) of D. russelii venom (1 mg/kg, i.v.) was significantly attenuated by artificial respiratory support, reducing the hypotensive effect to 42% (Fig. 2a). In contrast, the rapid cardiovascular collapse induced by E. ocellatus venom (50 µg/kg, i.v.) was not attenuated by artificial respiratory support (Figs. 1b and 2b).
To explore the effect of priming doses on both types of hypotensive responses, low dose P. textilis venom (2 µg/kg, i.v.) was administered 10 min prior to venom administration. A priming dose of P. textilis venom (i.e. 2 µg/kg, i.v.) had no significant effect on the subsequent addition of D. russelii venom (1 mg/kg, i.v.; Fig. 2a). In contrast, a priming dose of P. textilis venom (2 µg/kg, i.v.) prevented rapid cardiovascular collapse induced by E. ocellatus venom (50 µg/kg, i.v.; Fig. 2b), as did two sequential priming doses, but not one, of E. ocellatus venom (1 µg/kg, i.v.; Figs. 1c and 2b).
To further investigate the above effects of the venoms, a representative venom that caused collapse (i.e. P. textilis) and a representative venom that caused hypotension (i.e. D. russelii) were injected intramuscularly. Venom doses were increased to better mimic a bite scenario. P. textilis venom (20 mg/kg, i.m.; Table 2) caused collapse within 10 min of administration to the left bicep femoris muscle. D. russelii venom (50 mg/kg or 100 mg/kg, i.m.; Table 2) caused hypotension, but not collapse, within 30 min of administration.
PLA2 assay
All venoms had PLA2 activity. D. siamensis venom had the highest PLA2 activity, followed by B. gabonica, D. russelii and C. vegrandis venoms. P. textilis, B. arietans and E. ocellatus venoms had low PLA2 activity (Table 1).
Pro-coagulant assay
P. textilis venom had the most potent pro-coagulant activity (i.e. logEC50 = 1.29 ± 0.05 ng/ml; Fig. 3; Table 1), followed by D. russelii, D. siamensis and E. ocellatus venoms. C. vegrandis venom (logEC50 = 4.75 ± 0.04 ng/ml) had less pro-coagulant activity, and B. arietans and B. gabonica venoms had no detectable pro-coagulant activity (Fig. 3; Table 1).
In vitro myography experiments
D. russelii venom (1–1000 ng/ml) was a potent vasorelaxant (EC50 = 82.2 ± 15.3 ng/ml, Rmax = 91 ± 1%; Fig. 4a) in small mesenteric arteries. D. siamensis venom was a less potent vasodilator than D. russelii venom with an EC50 value of ~700 ng/ml and a relaxation response at 1000 ng/ml of 66 ± 15%. P. textilis venom caused < 50% relaxation (38.6 ± 9%) whilst, E. ocellatus, B. arientans, B. gabonica and C. vegrandis venoms induced < 30% relaxation (Fig. 4).
Discussion
We have demonstrated two distinct patterns of cardiovascular effects caused by the intravenous administration of different snake venoms. The first group of venoms cause a rapid decrease in blood pressure, often without recovery. We refer to this as ‘rapid cardiovascular collapse’ and it is the same phenomenon that we have previously described with Australian elapid venom15. A defining feature of this hypotensive response is that it is attenuated by sub-toxic ‘priming’ doses of venom of the same, or different snake species15. Snake venoms reported to induce this effect include P. textilis and E. ocellatus in this study, and previously, O. scutellatus (Coastal taipan)14. The second group of venoms, which include D. russelii and D. siamensis, caused a slower and prolonged decrease in blood pressure, with recovery occurring in most cases. In contrast to the first group, the drop in blood pressure is not prevented by prior administration of priming doses. We refer to this effect as ‘prolonged hypotension’.
We have previously postulated that the attenuation of the hypotensive effect with prior administration of smaller sub-toxic doses of venom is due to the pre-release, and depletion, of mediators which induce collapse15. This phenomenon was observed in the current study in which smaller priming doses of E. ocellatus venom or P. textilis venom prevented cardiovascular collapse caused by a larger dose of E. ocellatus venom. This suggests that these venoms are inducing their cardiovascular effects via a common mechanism.
For a high dose of D. russelii venom (i.e. 1 mg/kg), a response similar to rapid cardiovascular collapse occurred. However, when the rat was placed on a ventilator prior to administration of venom, this so called ‘collapse’ was prevented. In contrast, when rats administered E. ocellatus venom were placed on the ventilator, rapid cardiovascular collapse still occurred. The reasons for the protective effects of supportive respiration are unclear. We have previously shown that the neurotoxins present in D. russelii venom are relatively weak22. However, given that a rat has approximately 64 ml of circulating blood per kg body weight, an intravenous dose of 1 mg/kg of venom leads to a blood concentration of approximately 16 µg/ml. This very high venom concentration may be sufficient to cause paralysis of the diaphragm given that a 30 ng/ml concentration of the same venom caused complete neuromuscular blockade in the chick biventer nerve-muscle preparation22. Therefore, it could be argued that artificial respiration is preventing or overcoming the paralytic effects of the neurotoxins on the rat diaphragm. The different effects of supportive respiration on the cardiovascular effects of the venoms also supports the fact that collapse due to E. ocellatus venom occurs via a different mechanism. These studies were conducted in vivo using ketamine/xylazine as anesthesia, which may have affected the blood pressure, although ketamine is more likely to cause a slight increase in blood pressure.
To ensure that these cardiovascular effects seen in the in vivo model occurs in an actual snake bite, the effects of P. textilis venom and D. russelii venom were also tested via intramuscular administration. At 20 mg/kg (i.m.), P. textilis venom caused collapse within 10 min of administration. This delay in response is likely to be due to the time it takes for the venom to be absorbed. In contrast, when D. russelii venom was administered via intramuscular injection prolonged hypotension occurred, similar to that observed when venom was administrated intravenously. Even at 100 mg/kg concentration, collapse did not occur, further highlighting that both collapse and hypotension are not dose-dependent responses but represent two distinct cardiovascular effects.
There are many factors that could lead to venom-induced hypotension11, as distinct from cardiovascular collapse. Some snake venoms have highly evolved toxins such as calciseptine, FS2 toxins, C10S2C2 and S4C8 which block L-type Ca2+ currents23,24. Increasing capillary permeability protein (ICPP), isolated from Blunt-nosed viper (V. lebtina) venom is similar in potency and structure to vascular endothelial growth factor (VEGF) and is responsible for increasing vascular permeability25. Natriuretic peptides found in Green Mamba (D. angusticeps) venom26 and bradykinin potentiating peptides found in Bothrops spp. are also potent vaso-relaxants10,27,28. In the current study, D. russelii venom caused concentration-dependent relaxation of rat small mesenteric arteries suggesting peripheral vasodilation contributes to the prolonged hypotension observed in vivo. D. siamensis venom was also an efficacious dilator of rat small mesnteric arteries, though less potent than D. russelii venom. In contrast, the venoms which had a modest hypotensive effect in vivo (B. arientans, C. vegrandis and B. gabonica) were poor vasorelaxants of isolated mesenteric arteries. Although vasorelaxant responses can exhibit heterogeneity throughout the vasculature, the mesenteric vascular bed was chosen for this study given it makes a significant contribution to overall total peripheral resistance, receiving 25% of total cardiac output. As such, characterising vasorelaxation responses in these small mesenteric arteries (approx. 300microns in diameter), is of physiological relevance to blood pressure control. Gaboon viper (B. gabonica) venom has been shown to induce vasodilation resulting in a drop in peripheral resistance, leading to reduction in stroke volume due to cardiotoxins29. In another study using isolated heart preparations, Rhinoceros viper (B. nasicornis) venom produced an increase in left ventricular pressure, pacemaker activity and heart rate, indicating that the venom contains toxins that disrupt [Ca2+] and ion conductance30.
PLA2 toxins are ubiquitous components of snake venoms and display an array of activities including neurotoxicity, myotoxicity, cardiotoxicity, anti-coagulation, haemolytic, hypotensive and local tissue necrotic activity31. Interestingly, P. textilis and E. ocellatus venom, which induced rapid cardiovascular collapse, had the lowest PLA2 activity, whereas Daboia spp. had the highest amount of PLA2 activity. Therefore, there does not seem to be a link between PLA2 activity and cardiovascular collapse, although these toxins may contribute, directly or indirectly, to prolonged hypotension via vasodilation.
Daboia spp. and Pseudonaja spp. contain pro-coagulants factors in their venom32. While both P. textilis and E. ocellatus venoms caused rapid cardiovascular collapse in vivo, P. textilis venom was most potent in causing coagulation while E. ocellatus venom possessed comparatively less pro-coagulant activity. D. russelii and D. siamensis venom also caused coagulation. D. russelii and D. siamensis venoms are known to contain Factor X33,34 while both E. ocellatus35 and P. textilis venom contain prothrombin activators21,36,37. Therefore, pro-coagulant activity is unlikely to be directly related to the cardiovascular collapse induced by the venoms.
In conclusion, we have shown that the in vivo cardiovascular effects of venom include, at least, two distinct phenomena i.e. rapid cardiovascular collapse and prolonged hypotension and that both effects involve different mechanisms. Rapid cardiovascular collapse has a sudden onset and appears to be mediated by depletable endogenous mediators. In contrast, prolonged hypotension has a slower onset and appears to be due mainly to vasodilation.
Methods
Materials
Drugs and materials used were ketamine (Ceva Animal Health, Australia), xylaxine (Troy Laboratories Pty, Ltd, Australia), heparin (Hospira, Germany), bovine serum albumin (Sigma, USA), and fresh frozen plasma (Australian Red Cross). D. siamensis, P. textilis, B. arietans, B. gabonica and C. vegrandis venoms were obtained from Venom Supplies (Australia). D. russelii venom was a gift from Professor A. Gnanadasan (University of Colombo). E. ocellatus venom was a gift from the Liverpool School of Tropical Medicine. For procoagulant assays, venom (1 mg/mL) was prepared in 0.5% bovine serum albumin/tris-buffered saline and stored at −20 °C. Dilutions were prepared in 0.5% BSA/TBS immediately before use.
Animal experiments were approved by the Monash University Ethics Committee (MARP/2014/097 and MARP/2017/147). All experiments were performed in accordance with relevant guidelines and regulations.
Anaesthetised rats
Male Sprague-Dawley rats (280–350 g) were anaesthetised with a mixture of ketamine (100 mg/kg, i.p.) and xylazine (10 mg/kg, i.p.). Ketamine/xylazine cocktail was used as it provides sedation and muscle relaxation as well as deep analgesia and anesthesia without compromising blood pressure. A midline incision was made and a cannula inserted into the trachea for mechanical ventilation (~1 ml/100 g of body weight at 55 strokes/min) if required. Cannulae were inserted into the left jugular vein for administration of venom and the right carotid artery to record arterial blood pressure. The arterial cannula was connected to a pressure transducer. Blood pressure was then allowed to stabilise for approximately 10–15 min. Body temperature was maintained at 37 °C using an overhead lamp and heated dissection table. Venom was administered via the jugular vein followed by flushing with saline or via a bolus administration into the left bicep femoralis muscle. Responses to venom were measured as percentage change in mean arterial pressure (MAP).
Myograph experiments
Male Sprague-Dawley rats (200–250 g) were euthanized by CO2 inhalation (95% CO2, 5% O2) followed by cervical dislocation. Small mesenteric arteries (third-order branch of the superior mesenteric artery) were isolated, cut into 2 mm lengths, and mounted in isometric myograph baths. Vessels were maintained in physiological salt solution, composed of (in mM): 119 NaCl, 4.7 KCl, 1.17 MgSO4, 25 NaHCO3, 1.8 KH2PO4, 2.5 CaCl2, 11 glucose, and 0.026 EDTA, at 37 °C and supplied with carbogen (95% O2; 5% CO2). The mesenteric arteries were allowed to equilibrate for 30 min under zero force and then a 5 mN resting tension was applied. Changes in isometric tension were recorded using Myography Interface Model 610 M version 2.2 (ADInstruments, Pty Ltd, USA) and a chart recorder (Yokogawa, Japan). Following a 15 min equilibration period at 5 mN, the mesenteric arteries were contracted maximally (Fmax) using a K+ depolarizing solution [K+-containing physiological salt solution (KPSS); composed of (in mM) 123 KCl, 1.17 MgSO4, 1.18 KH2PO4, 2.5 CaCl2, 25 NaHCO3, and 11 glucose]. The integrity of the endothelium was confirmed by relaxation to acetylcholine (ACh, 10 µM) in tissues pre-contracted with the thromboxane A2 mimetic, U46619 (1 µM), then washed with physiological salt solution and the tension allowed to return to baseline. Relaxation of >80% to ACh was used to indicate vessels with an intact endothelium. There were no significant differences in response to ACh between the groups studied. If endothelial damage was evident (ACh relaxation <80%) then the vessel was not used for experimentation. Cumulative concentration-response curves to venom (1 ng/ml-1µg/ml) were constructed in vessels pre-contracted with titrated concentrations of U46619 (~50% Fmax). Sodium nitroprusside (SNP, 10 µM) was added at the end of each concentration-response curve to ensure maximum relaxation. Only one concentration-response curve to venom was obtained in each vessel segment38,39.
Pro-coagulation assay
Aliquots (10 ml) of fresh frozen plasma were thawed at 37 °C, then spun at 2500 rpm for 10 min. Venom solutions (100 µL) were placed in the wells of a 96 well microtitre plate at room temperature or at 37 °C in a BioTek ELx808 plate reader. Plasma (100 µL) and calcium (0.2 M/ml) were then added simultaneously to each well using a multichannel pipette. After a 5 s shake step for mixing, the optical density at 340 nm was monitored every 30 s over 20 min40.
PLA2 assay
PLA2 activity of the venoms was determined using a secretory PLA2 colourmetric assay kit (Cayman Chemical; MI, USA) according to manufacturer’s instructions. This assay used 1, 2-dithio-analogue of diheptanoyl phosphatidylcholine, which serves as a substrate for PLA2 enzymes. Free thiols generated following the hydrolysis of the thioester bond at the sn-2 position by PLA2 are detected using DTNB (5, 5′-dithio-bis-[2-nitrobenzoic acid]). Colour changes were monitored at 405 nm in a fusion α microplate reader (PerkinElmer; MA, USA), sampling every minute for a 5 min period. PLA2 activity was expressed as micromoles of phosphatidylcholine hydrolysed per minute per milligram of enzyme2.
Statistical analysis
For the anaesthetized rat experiments, pulse pressure was defined as the difference between systolic and diastolic blood pressures. Mean arterial pressure (MAP) was calculated as diastolic blood pressure plus one-third of pulse pressure. These data were tested using a D’Agostino-Pearson normality test and found to be normally distributed. Therefore, differences in MAP between treatment groups were analysed using a one-way ANOVA with Dunnett’s multiple comparison test. Sample sizes are based on the number of animals required to provide >85% power to detect an effect size of 35% with a confidence level (α) of 5% for the in vivo endpoint measure of blood pressure (standard deviation (SD) <15%). This ensured that experimental design was sufficiently powered.
For the myography experiments, blood vessel relaxation was expressed as a percentage reversal of the U46619 pre-contraction. Individual relaxation curves to D. russelii venom were fitted to a sigmoidal logistic equation and EC50 values (concentration of agonist resulting in a 50% relaxation) calculated41. Where EC50 values could not be obtained, concentration-response curves to venoms were compared by means of a two-way repeated measures ANOVA (n = number of artery segments from separate animals). Data represent the mean ± SEM (error bars on graph). Statistical significance was defined as P < 0.05. All data analysis was performed using GraphPad Prism version 5.02 (GraphPad Software, San Diego, CA, USA).
For the coagulation assay, responses were plotted as 30 s/[clotting time(s)] against the logarithm of the venom concentration. This provided a normalised measure of the clotting effect and produced normalised concentration-clotting curves, which were fitted with a standard sigmoidal curve (Hill slope = 1) to calculate the effective concentration 50 (EC50). The EC50 is the concentration of venom that resulted in a pro-coagulant effect halfway between no clotting effect and maximal clotting effect42.
References
Casewell, N. R., Wüster, W., Vonk, F. J., Harrison, R. A. & Fry, B. G. Complex cocktails: the evolutionary novelty of venoms. Trends Ecol. & Evolution 28, 219–229 (2013).
Chaisakul, J., Konstantakopoulos, N., Smith, A. I. & Hodgson, W. C. Isolation and characterisation of P-EPTX-Ap1a and P-EPTX-Ar1a: pre-synaptic neurotoxins from the venom of the northern (Acanthophis praelongus) and Irian Jayan (Acanthophis rugosus) death adders. Biochemical Pharmacology 80, 895–902 (2010).
Barber, C. M., Isbister, G. K. & Hodgson, W. C. Alpha neurotoxins. Toxicon 66, 47–58 (2013).
Kuruppu, S., Smith, A. I., Isbister, G. K. & Hodgson, W. C. Neurotoxins from Australo-Papuan elapids: a biochemical and pharmacological perspective. Crit. Rev. Toxicol. 38, 73–86 (2008).
Wickramaratna, J. C., Fry, B. G., Aguilar, M. I., Kini, R. M. & Hodgson, W. C. Isolation and pharmacological characterization of a phospholipase A2 myotoxin from the venom of the Irian Jayan death adder (Acanthophis rugosus). Br. J. Pharmacology 138, 333–342 (2003).
Silva, A. et al. Clinical and pharmacological investigation of myotoxicity in Sri Lankan Russell’s viper (Daboia russelii) envenoming. PLoS Neglected Tropical Dis. 10, e0005172 (2016).
Gutiérrez, J. & Lomonte, B. Phospholipase A2 myotoxins from Bothrops snake venoms. Toxicon 33, 1405–1424 (1995).
Gutiérrez, J. M. & Lomonte, B. Phospholipases A2: unveiling the secrets of a functionally versatile group of snake venom toxins. Toxicon 62, 27–39 (2013).
Isbister, G. K., Brown, S. G., MacDonald, E., White, J. & Currie, B. J. Current use of Australian snake antivenoms and frequency of immediate-type hypersensitivity reactions and anaphylaxis. Med. J. Aust. 188, 473 (2008).
Joseph, R., Pahari, S., Hodgson, W. C. & Kini, R. M. Hypotensive agents from snake venoms. Curr. Drug. Targets-Cardiovascular & Hematological Disord. 4, 437–459 (2004).
Hodgson, W. C. & Isbister, G. K. The application of toxins and venoms to cardiovascular drug discovery. Curr. Opin. Pharmacol. 9, 173–176 (2009).
Moore, R. S. Second-degree heart block associated with envenomation by Vipera berus. Emerg. Med. J. 5, 116–118 (1988).
Koh, C. Y. & Kini, R. M. From snake venom toxins to therapeutics–cardiovascular examples. Toxicon 59, 497–506 (2012).
Chaisakul, J. et al. In vivo and in vitro cardiovascular effects of Papuan taipan (Oxyuranus scutellatus) venom: Exploring “sudden collapse”. Toxicol. Lett. 213, 243–248 (2012).
Chaisakul, J., Isbister, G. K., Kuruppu, S., Konstantakopoulos, N. & Hodgson, W. C. An examination of cardiovascular collapse induced by eastern brown snake (Pseudonaja textilis) venom. Toxicol. Lett. 221, 205–211 (2013).
Currie, B. J. Snakebite in tropical Australia, Papua New Guinea and Irian Jaya. Emerg. Med. 12, 285–294 (2000).
Allen, G. E. et al. Clinical Effects and Antivenom Dosing in Brown Snake (Pseudonaja spp.) Envenoming - Australian Snakebite Project (ASP-14). PLoS ONE 7, e53188, https://doi.org/10.1371/journal.pone.0053188 (2012).
Johnston, M. A., Fatovich, D. M., Haig, A. D. & Daly, F. F. Successful resuscitation after cardiac arrest following massive brown snake envenomation. Med. J. Aust. 177, 646–648 (2002).
Johnston, C. I. et al. The Australian snakebite project, 2005–2015 (ASP-20). Med. J. Aus.t 207, 119–125 (2017).
Tibballs, J. The cardiovascular, coagulation and haematological effects of tiger snake (Notechis scutatus) venom. Anaesth. Intensive Care 26, 529 (1998).
Tibballs, J., Sutherland, S., Rivera, R. & Masci, P. The cardiovascular and haematological effects of purified prothrombin activator from the common brown snake (Pseudonaja textilis) and their antagonism with heparin. Anaesth. Intensive Care 20, 28–32 (1992).
Silva, A. et al. Neurotoxicity in Sri Lankan Russell’s viper (Daboia russelii) envenoming is primarily due to U1-viperitoxin-Dr1a, a pre-synaptic neurotoxin. Neurotox. Res. 31, 11–19 (2017).
de Weille, J. R., Schweitz, H., Maes, P., Tartar, A. & Lazdunski, M. Calciseptine, a peptide isolated from black mamba venom, is a specific blocker of the L-type calcium channel. Proc. Nat. Acad. Sci. 88, 2437–2440 (1991).
Watanabe, T. X. et al. Smooth muscle relaxing and hypotensive activities of synthetic calciseptine and the homologous snake venom peptide FS2. Japanese J. Pharmacol. 68, 305–313 (1995).
Gasmi, A. et al. Purification and characterization of a growth factor-like which increases capillary permeability from Vipera lebetina venom. Biochemical Biophysical Res. Commun. 268, 69–72 (2000).
Schweitz, H., Vigne, P., Moinier, D., Frelin, C. & Lazdunski, M. A new member of the natriuretic peptide family is present in the venom of the green mamba (Dendroaspis angusticeps). J. Biol. Chem. 267, 13928–13932 (1992).
Cintra, A. C., Vieira, C. A. & Giglio, J. R. Primary structure and biological activity of bradykinin potentiating peptides from Bothrops insularis snake venom. J. Protein Chem. 9, 221–227 (1990).
Ferreira, S. & E. Silva, M. R. Potentiation of bradykinin and eledoisin by BPF (bradykinin potentiating factor) from Bothrops jararaca venom. Experientia 21, 347–349 (1965).
Adams, Z. S. et al. The effect of Bitis gabonica (Gaboon viper) snake venom on blood pressure, stroke volume and coronary circulation in the dog. Toxicon 19, 263–270 (1981).
Alloatti, G. et al. The mechanical effects of rhinoceros horned viper (Bitis nasicornis) venom on the isolated perfused guinea-pig heart. Exp. Physiol. 76, 611–614 (1991).
Tasoulis, T. & Isbister, G. K. A review and database of snake venom proteomes. Toxins 9, 290 (2017).
Maduwage, K. & Isbister, G. K. Current treatment for venom-induced consumption coagulopathy resulting from snakebite. PLoS Neglected Tropical Dis. 8, e3220 (2014).
Mukherjee, A. K. Characterization of a novel pro-coagulant metalloprotease (RVBCMP) possessing α-fibrinogenase and tissue haemorrhagic activity from venom of Daboia russelli russelli (Russell’s viper): Evidence of distinct coagulant and haemorrhagic sites in RVBCMP. Toxicon 51, 923–933 (2008).
Mukherjee, A. K. & Mackessy, S. P. Biochemical and pharmacological properties of a new thrombin-like serine protease (Russelobin) from the venom of Russell’s Viper (Daboia russelii russelii) and assessment of its therapeutic potential. Biochimica et. Biophysica Acta (BBA)-General Subj. 1830, 3476–3488 (2013).
Hasson, S., Theakston, R. D. G. & Harrison, R. Cloning of a prothrombin activator-like metalloproteinase from the West African saw-scaled viper, Echis ocellatus. Toxicon 42, 629–634 (2003).
Rao, V. S., Swarup, S. & Kini, R. M. The nonenzymatic subunit of pseutarin C, a prothrombin activator from eastern brown snake (Pseudonaja textilis) venom, shows structural similarity to mammalian coagulation factor V. Blood 102, 1347–1354 (2003).
Chaisakul, J. et al. Prothrombin activator-like toxin appears to mediate cardiovascular collapse following envenoming by Pseudonaja textilis. Toxicon 102, 48–54 (2015).
Favaloro, J. L. & Kemp-Harper, B. K. Redox variants of NO (NO· and HNO) elicit vasorelaxation of resistance arteries via distinct mechanisms. Am. J. Physiol.-Heart Circulatory Physiology 296, H1274–H1280 (2009).
Yuill, K. H., Yarova, P., Kemp-Harper, B. K., Garland, C. J. & Dora, K. A. A novel role for HNO in local and spreading vasodilatation in rat mesenteric resistance arteries. Antioxid. & Redox Signal. 14, 1625–1635 (2011).
O’Leary, M. A. & Isbister, G. K. A turbidimetric assay for the measurement of clotting times of procoagulant venoms in plasma. J. Pharmacol. Toxicol. Meth. 61, 27–31 (2010).
Andrews, K. L. et al. A role for nitroxyl (HNO) as an endothelium-derived relaxing and hyperpolarizing factor in resistance arteries. Brit. J. Pharmacol. 157, 540–550 (2009).
Maduwage, K. P., Scorgie, F. E., Lincz, L. F., O’Leary, M. A. & Isbister, G. K. Procoagulant snake venoms have differential effects in animal plasmas: Implications for antivenom testing in animal models. Thrombosis Res. 137, 174–177 (2016).
Acknowledgements
This study was funded by an Australian National Health and Medical Research Council (NHMRC) Senior Research Fellowship (ID: 1061041) awarded to G.K.I. and a NHMRC Centres for Research Excellence Grant ID: 1110343 awarded to G.K.I. and W.C.H.
Author information
Authors and Affiliations
Contributions
R.K., W.C.H., B.K.-H. and G.K.I. designed the study. R.K., W.C.H. and B.K.-H. conducted experiments. R.K. analyzed the data. W.C.H. and R.K. prepared the figures. R.K. wrote the initial manuscript text. B.K.-H., A.S., S.K., G.K.I. and W.C.H. reviewed the manuscript and contributed to experimental design.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Kakumanu, R., Kemp-Harper, B.K., Silva, A. et al. An in vivo examination of the differences between rapid cardiovascular collapse and prolonged hypotension induced by snake venom. Sci Rep 9, 20231 (2019). https://doi.org/10.1038/s41598-019-56643-0
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-019-56643-0
This article is cited by
-
A lipidomics approach reveals new insights into Crotalus durissus terrificus and Bothrops moojeni snake venoms
Archives of Toxicology (2021)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.