In vitro and in vivo preclinical venom inhibition assays identify metalloproteinase inhibiting drugs as potential future treatments for snakebite envenoming by Dispholidus typus

Menzies, Stefanie ORCID: https://orcid.org/0000-0002-9273-9296, Clare, Rachel ORCID: https://orcid.org/0000-0002-3945-0530, Xie, Chunfang, Westhorpe, Adam, Hall, Steven, Edge, Becky, Al Solaiss, Jaffer, Crittenden, Edouard, Marriott, Amy, Harrison, Robert, Kool, Jeroen and Casewell, Nicholas ORCID: https://orcid.org/0000-0002-8035-4719 (2022) 'In vitro and in vivo preclinical venom inhibition assays identify metalloproteinase inhibiting drugs as potential future treatments for snakebite envenoming by Dispholidus typus'. Toxicon, Vol 14, p. 100118.

Preview

Text 1-s2.0-S2590171022000285-main.pdf - Published Version Available under License Creative Commons Attribution. Download (2MB) | Preview

Abstract

Snakebite envenoming affects more than 250,000 people annually in sub-Saharan Africa. Envenoming by Dis-pholidus typus (boomslang) results in venom-induced consumption coagulopathy (VICC), whereby highly abun-dant prothrombin-activating snake venom metalloproteinases (SVMPs) consume clotting factors and deplete fibrinogen. The only available treatment for D. typus envenoming is the monovalent SAIMR Boomslang anti-venom. Treatment options are urgently required because this antivenom is often difficult to source and, at US $6000/vial, typically unaffordable for most snakebite patients. We therefore investigated the in vitro and in vivo preclinical efficacy of four SVMP inhibitors to neutralise the effects of D. typus venom; the matrix metal-loproteinase inhibitors marimastat and prinomastat, and the metal chelators dimercaprol and DMPS. The venom of D. typus exhibited an SVMP-driven procoagulant phenotype in vitro. Marimastat and prinomastat demonstrated equipotent inhibition of the SVMP-mediated procoagulant activity of the venom in vitro, whereas dimercaprol and DMPS showed considerably lower potency. However, when tested in preclinical murine models of enve-noming using mixed sex CD1 mice, DMPS and marimastat demonstrated partial protection against venom lethality, demonstrated by prolonged survival times of experimental animals, whereas dimercaprol and prino-mastat failed to confer any protection at the doses tested. The preclinical results presented here demonstrate that DMPS and marimastat show potential as novel small molecule-based therapeutics for D. typus snakebite enve-noming. These two drugs have been previously shown to be effective against Echis ocellatus VICC in preclinical models, and thus we conclude that marimastat and DMPS should be further explored as potentially valuable early intervention therapeutics to broadly treat VICC following snakebite envenoming in sub-Saharan Africa.

Item Type:	Article
Subjects:	QV Pharmacology > Toxicology > General Toxicology > QV 601 Antidotes and other therapeutic measures WD Disorders of Systemic, Metabolic or Environmental Origin, etc > Animal Poisons > WD 410 Reptiles
Faculty: Department:	Biological Sciences > Department of Tropical Disease Biology
Digital Object Identifer (DOI):	https://doi.org/10.1016/j.toxcx.2022.100118
Depositing User:	Cathy Waldron
Date Deposited:	22 Mar 2022 13:00
Last Modified:	22 Mar 2022 13:00
URI:	https://archive.lstmed.ac.uk/id/eprint/20151

Statistics

View details

Actions (login required)

Edit Item