Kowalski Krzysztof, Marciniak Paweł, Rosiński Grzegorz, Rychlik Leszek
Department of Systematic Zoology, Institute of Environmental Biology, Adam Mickiewicz University, Umultowska 89, 61-614 Poznań, Poland.
Department of Animal Physiology and Development, Institute of Experimental Biology, Faculty of Biology, Adam Mickiewicz University, Umultowska 89, 61-614 Poznań, Poland.
Front Zool. 2017 Sep 30;14:46. doi: 10.1186/s12983-017-0230-0. eCollection 2017.
Animal toxins can have medical and therapeutic applications. Principally, toxins produced by insects, arachnids, snakes and frogs have been characterized. Venomous mammals are rare, and their venoms have not been comprehensively investigated. Among shrews, only the venom of has been analysed so far, and blarina toxin has been proven to be its main toxic component. It is assumed that employs its venom to hunt larger prey. However, the toxic profile, properties and mode of action of its venom are largely unknown. Therefore, we analysed the cardio-, myo- and neurotropic properties of venom and saliva of non-venomous (control tests) in vitro in physiological bioassays carried out on two model organisms: beetles and frogs. For the first time, we fractionated venom and saliva by performing chromatographic separation. Next, the properties of selected compounds were analysed in cardiotropic bioassays in the heart.
The venom of caused a high decrease in the conduction velocity of the frog sciatic nerve, as well as a significant decrease in the force of frog calf muscle contraction. We also recorded a significant decrease in the frog heart contractile activity. Most of the selected compounds from venom displayed a positive chronotropic effect on the beetle heart. However, one fraction caused a strong decrease in the heart contractile activity coupled with a reversible cardiac arrest. We did not observe any responses of the insect heart and frog organs to the saliva of . Preliminary mass spectrometry analysis revealed that calmodulin-like protein, thymosin β-10, hyaluronidase, lysozyme C and phospholipase A2 are present in the venom of , whereas thymosin β4, lysozyme C and β-defensin are present in saliva.
Our results showed that venom has stronger paralytic properties and lower cardioinhibitory activity. Therefore, it is highly probable that might use its venom as a prey immobilizing agent. We also confirmed that is not a venomous mammal because its saliva did not exhibit any toxic effects.
动物毒素具有医学和治疗应用价值。主要对昆虫、蛛形纲动物、蛇和青蛙产生的毒素进行了表征。有毒哺乳动物较为罕见,其毒液尚未得到全面研究。在鼩鼱中,到目前为止仅分析了[某一种鼩鼱]的毒液,且已证明布拉里纳毒素是其主要毒性成分。据推测,[某一种鼩鼱]利用其毒液捕食更大的猎物。然而,其毒液的毒性特征、性质和作用方式在很大程度上尚不清楚。因此,我们在对两种模式生物(甲虫和青蛙)进行的生理生物测定中,体外分析了[某一种鼩鼱]毒液以及无毒[另一种鼩鼱](对照试验)唾液的心脏、肌肉和神经趋向性特性。我们首次通过色谱分离对[某一种鼩鼱]毒液和[另一种鼩鼱]唾液进行了分级分离。接下来,在[某一种鼩鼱]心脏的变时生物测定中分析了所选化合物的特性。
[某一种鼩鼱]的毒液导致青蛙坐骨神经传导速度大幅下降,以及青蛙小腿肌肉收缩力显著降低。我们还记录到青蛙心脏收缩活动显著下降。从[某一种鼩鼱]毒液中选取的大多数化合物对甲虫心脏显示出正性变时作用。然而,一个级分导致[某一种鼩鼱]心脏收缩活动强烈下降并伴有可逆性心脏骤停。我们未观察到昆虫心脏和青蛙器官对[另一种鼩鼱]唾液有任何反应。初步质谱分析表明,钙调蛋白样蛋白、胸腺素β - 10、透明质酸酶、溶菌酶C和磷脂酶A2存在于[某一种鼩鼱]的毒液中,而胸腺素β4、溶菌酶C和β - 防御素存在于[另一种鼩鼱]的唾液中。
我们的结果表明,[某一种鼩鼱]的毒液具有更强的麻痹特性和更低的心脏抑制活性。因此,[某一种鼩鼱]很可能将其毒液用作猎物固定剂。我们还证实[另一种鼩鼱]不是有毒哺乳动物,因为其唾液未表现出任何毒性作用。