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尼日利亚毒蛇锯鳞蝰和鼓腹咝蝰毒液的毒理学分析。

Toxicological analyses of the venoms of Nigerian vipers Echis ocellatus and Bitis arietans.

作者信息

Dingwoke Emeka John, Adamude Fatima Adis, Salihu Aliyu, Abubakar Mujitaba Suleiman, Sallau Abdullahi Balarabe

机构信息

Department of Tropical Diseases, UNESCO-International Center for Biotechnology, University of Nigeria, Nsukka, Enugu State, Nigeria.

Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria, Kaduna State, Nigeria.

出版信息

Trop Med Health. 2024 Jan 29;52(1):15. doi: 10.1186/s41182-024-00581-9.


DOI:10.1186/s41182-024-00581-9
PMID:38282015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10823708/
Abstract

BACKGROUND: Among the medically important snakes in Nigeria, Echis ocellatus and Bitis arietans have the most lethal venom. These venoms were classified according to the presence of snake venom metalloproteinases (SVMPs), snake venom phospholipase A (PLAs), and snake venom serine proteases (SVSPs). Toxicological analyzes were performed to understand the significance of different protein families in venoms. METHODS: Proteins were separated from venom using column chromatography. The skin and footpad of mice were used to determine hemorrhagic and edematogenic activities. Caprine blood plasma was used to test fibrinolytic activity in vitro. RESULTS: The results showed that, compared to the crude venom, the SVMP fraction induced hemorrhagic effects with a diameter of 26.00 ± 1.00 mm in E. ocellatus and 21.33 ± 1.52 mm in B. arietans. Both SVSP and SVMP had anticoagulant effects; however, the SVSP fraction had a stronger effect, with a longer anticoagulation time of 30.00 ± 3.00 min in E. ocellatus and 26.00 ± 2.00 min in B. arietans. These main venom toxins, SVMPs, SVSPs, and PLA, were found to have edema-forming effects that were optimal at 2 h after envenomation. PLAs had the highest edema-inducing activity, with onset 30 min after envenomation. CONCLUSIONS: Given the importance of SVMPs in altering the integrity of the membrane structure and impairing the blood coagulation system, an antivenom that can specifically neutralize its activity could inhibit the hemorrhage effects of the venoms.

摘要

背景:在尼日利亚具有医学重要性的蛇类中,锯鳞蝰和鼓腹咝蝰拥有最致命的毒液。这些毒液根据蛇毒金属蛋白酶(SVMPs)、蛇毒磷脂酶A(PLAs)和蛇毒丝氨酸蛋白酶(SVSPs)的存在情况进行分类。进行了毒理学分析以了解毒液中不同蛋白质家族的重要性。 方法:使用柱色谱法从毒液中分离蛋白质。用小鼠的皮肤和足垫来测定出血和致水肿活性。用山羊血浆在体外测试纤溶活性。 结果:结果表明,与粗毒液相比,锯鳞蝰毒液中的SVMP组分诱导的出血效应直径为26.00±1.00毫米,鼓腹咝蝰毒液中的SVMP组分诱导的出血效应直径为21.33±1.52毫米。SVSP和SVMP均具有抗凝作用;然而,SVSP组分的作用更强,锯鳞蝰毒液中的抗凝时间更长,为30.00±3.00分钟,鼓腹咝蝰毒液中的抗凝时间为26.00±2.00分钟。发现这些主要的毒液毒素,即SVMPs、SVSPs和PLA,具有在注入毒液后2小时达到最佳效果的致水肿作用。PLAs具有最高的致水肿活性,在注入毒液后30分钟开始起效。 结论:鉴于SVMPs在改变膜结构完整性和损害血液凝固系统方面的重要性,一种能够特异性中和其活性的抗蛇毒血清可以抑制毒液的出血效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/da1eb7d34d51/41182_2024_581_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/ef4140231b25/41182_2024_581_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/cdda13edfe46/41182_2024_581_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/7231c83906a2/41182_2024_581_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/da1431593e7e/41182_2024_581_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/6ee43bbe0a82/41182_2024_581_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/da1eb7d34d51/41182_2024_581_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/ef4140231b25/41182_2024_581_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/eb7e0a186981/41182_2024_581_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/cdda13edfe46/41182_2024_581_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/7231c83906a2/41182_2024_581_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/da1431593e7e/41182_2024_581_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/6ee43bbe0a82/41182_2024_581_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/10823708/da1eb7d34d51/41182_2024_581_Fig7_HTML.jpg

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本文引用的文献

[1]
Venom proteomic analysis of medically important Nigerian viper and snake species.

Biochem Biophys Rep. 2021-11-2

[2]
Snakebite envenoming in different national contexts: Costa Rica, Sri Lanka, and Nigeria.

Toxicon X. 2021-5-25

[3]
Causes and Consequences of Snake Venom Variation.

Trends Pharmacol Sci. 2020-8

[4]
Toxinology provides multidirectional and multidimensional opportunities: A personal perspective.

Toxicon X. 2020-5-11

[5]
Beyond the 'big four': Venom profiling of the medically important yet neglected Indian snakes reveals disturbing antivenom deficiencies.

PLoS Negl Trop Dis. 2019-12-5

[6]
Snake Venom Hemotoxic Enzymes: Biochemical Comparison between Species from Central Mexico.

Molecules. 2019-4-16

[7]
The paraspecific neutralisation of snake venom induced coagulopathy by antivenoms.

Commun Biol. 2018-4-19

[8]
A Review and Database of Snake Venom Proteomes.

Toxins (Basel). 2017-9-18

[9]
Snakebite envenomation turns again into a neglected tropical disease!

J Venom Anim Toxins Incl Trop Dis. 2017-8-8

[10]
Preclinical Evaluation of the Efficacy of Antivenoms for Snakebite Envenoming: State-of-the-Art and Challenges Ahead.

Toxins (Basel). 2017-5-13

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