Isolation and Pharmacological Characterisation of Pre-Synaptic Neurotoxins from Thai and Javanese Russell's Viper ( Daboia siamensis ) Venoms

• Published in: Toxins 2024-09, Vol.16 (9), p.405
• Main Authors: Lay, Mimi, Hodgson, Wayne C
• Format: Article
• Language: English
• Subjects: Acetates; Animals; Antivenins - pharmacology; Antivenom; Chickens; Daboia; Fractions; Geographical distribution; Indoles; Keto Acids; Liquid chromatography; Male; Mass spectrometry; Muscles; Myotoxicity; neuromuscular junction; Neuromuscular Junction - drug effects; Neurotoxicity; neurotoxin; Neurotoxins; Neurotoxins - isolation & purification; Neurotoxins - toxicity; Pharmacology; Phospholipase A2; Phospholipase A2 Inhibitors - pharmacology; Phospholipases A2; Poisonous snakes; Proteases; Proteins; Russell’s viper; Scientific imaging; Skeletal muscle; Snake bites; snake venom; Southeast Asian People; Thailand; Toxicity; Toxins; Tubocurarine; Venom; Viper Venoms - toxicity
• ISSN: 2072-6651; 2072-6651
• DOI: 10.3390/toxins16090405

The widespread geographical distribution of Russell's vipers ( spp.) is associated with marked variations in the clinical outcomes of envenoming by species from different countries. This is likely to be due to differences in the quantity and potency of key toxins and, potentially, the presence or absence of some toxins in venoms across the geographical spectrum. In this study, we aimed to isolate and pharmacologically characterise the major neurotoxic components of venoms from Thailand and Java (Indonesia) and explore the efficacy of antivenom and a PLA inhibitor, Varespladib, against the neuromuscular activity. These data will provide insights into the link between venom components and likely clinical outcomes, as well as potential treatment strategies. Venoms were fractionated using RP-HPLC and the in vitro activity of isolated toxins assessed using the chick biventer cervicis nerve-muscle preparation. Two major PLA fractions (i.e., fractions 8 and 10) were isolated from each venom. Fraction 8 from both venoms produced pre-synaptic neurotoxicity and myotoxicity, whereas fraction 10 from both venoms was weakly neurotoxic. The removal of the two fractions from each venom abolished the in vitro neurotoxicity, and partially abolished myotoxicity, of the whole venom. A combination of the two fractions from each venom produced neurotoxic activity that was equivalent to the respective whole venom (10 µg/mL), but the myotoxic effects were not additive. The in vitro neurotoxicity of fraction 8 (100 nM) from each venom was prevented by the pre-administration of Thai Russell's viper monovalent antivenom (2× recommended concentration) or preincubation with Varespladib (100 nM). Additionally, the neurotoxicity produced by a combination of the two fractions was partially reversed by the addition of Varespladib (100-300 nM) 60 min after the fractions. The present study demonstrates that the in vitro skeletal muscle effects of Thai and Javanese venoms are primarily due to key PLA toxins in each venom.