Literature DB >> 31722041

Comparative study of the in vivo toxicity and pathophysiology of envenomation by three medically important Egyptian snake venoms.

Tarek M Abd El-Aziz1,2, Mahmoud I Shoulkamy3,4, Ahmed M Hegazy3, James D Stockand5, Ahmed Mahmoud6, Ashraf M A Mashaly3.   

Abstract

Snakebite envenomation is a serious medical problem in many developing tropical and subtropical countries. Envenomation is registered by the World Health Organization as a neglected tropical disease due to critical shortages in the production of antivenom. Envenomation causes more than 100,000 deaths annually. Snakebites result in several effects to include edema, blistering, hemorrhage, necrosis and respiratory paralysis. Antivenom is the preferred treatment for the systemic effects of snakebite envenomation, though these are often ineffective in neutralizing venom toxin-induced local tissue damage. To effectively treat snakebites, it is important to determine the lethal potency and pathophysiological effects induced by specific snake venoms. In the current study, we compared the lethality, and the hemorrhagic and dermonecrotic activities of venoms from three snakes in Egypt that are the primary causes of local tissue necrosis. Our data show that the intraperitoneal median lethal doses (LD50) for Cerastes cerastes, Echis carinatus and Naja nigricollis venoms are 0.946, 1.744 and 0.341 mg/kg mouse body weight, respectively. These results indicated that N. nigricollis venom is the most toxic and significantly accelerated the time of death compared to the other two venoms. However, no hematoma or associated edema appeared upon sub-plantar injection of N. nigricollis venom into the mice hind paw. Two hours following intradermal injection of C. cerastes and E. carinatus venoms, macroscopic analysis of the inner surface of mouse skin showed severe hemorrhagic lesions, whereas only insignificant hemorrhagic lesion appeared in mice injected with the highest dose of N. nigricollis venom. Furthermore, the minimum necrotic doses (MND) for the same venoms were 43.15, and 70.87 µg/mouse, or not observed in the case of N. nigricollis venom, respectively. These LD50 values and pathophysiological results can be used to guide development of antivenom against bites by these dangerous Egyptian snakes.

Entities:  

Keywords:  Antivenom production; Envenomation; Hemorrhage; In vivo toxicity; Pathophysiology; Snake venoms; Snakebites

Year:  2019        PMID: 31722041     DOI: 10.1007/s00204-019-02619-y

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  4 in total

1.  Therapeutic Outcome of Anti-inflammatory and Antioxidative Medicines on the Dermonecrotic Activity of Cerastes cerastes Venom.

Authors:  Abderrezak Khelfi; Habiba Oussedik-Oumehdi; Fatima Laraba-Djebari
Journal:  Inflammation       Date:  2022-03-05       Impact factor: 4.092

Review 2.  Advances in venomics: Modern separation techniques and mass spectrometry.

Authors:  Tarek Mohamed Abd El-Aziz; Antonio G Soares; James D Stockand
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2020-09-17       Impact factor: 3.205

3.  New aspects in snake venom toxicology.

Authors:  Hermann M Bolt
Journal:  Arch Toxicol       Date:  2021-05-06       Impact factor: 5.153

4.  Improved up-and-down procedure for acute toxicity measurement with reliable LD50 verified by typical toxic alkaloids and modified Karber method.

Authors:  Yan-Yu Zhang; Yu-Feng Huang; Jie Liang; Hua Zhou
Journal:  BMC Pharmacol Toxicol       Date:  2022-01-04       Impact factor: 2.483

  4 in total

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