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从宽带水蛇蛇毒中分离出的具有肌毒性的天冬氨酸49磷脂酶A2(ACL-I PLA2)对离体蟾蜍膀胱水转运的影响。

Effects of a myotoxic Asp49 phospholipase A2 (ACL-I PLA2) isolated from Agkistrodon contortrix laticinctus snake venom on water transport in the isolated toad urinary bladder.

作者信息

Leite R S, Ramos O H P, Gomes A R S, Salvini T F, Souza D H F, Franco W, Selistre-de-Araujo H S

机构信息

Departamento de Ciências Fisiológicas, Universidade Federal de São Carlos, Rodovia Washington Luís, Km 235, São Carlos, SP, 13565-905, Brazil.

出版信息

Toxicon. 2004 Jun 1;43(7):847-53. doi: 10.1016/j.toxicon.2004.03.019.

Abstract

An Asp49 PLA2 (ACL-I PLA2) was purified from the venom of Agkistrodon contortrix laticinctus by gel filtration and cation-exchange chromatography. It has a relative molecular mass of 14,000, and its N-terminal sequence has more than 65% of identity with other snake venom PLA2s. ACL-I PLA2 injected into the Tibialis anterior muscle of rats and mice at doses of 0.3 and 1.6 mg/kg, respectively, induced muscle fiber necrosis, cellular infiltration and edema 3 and 48 h after injection. The effect of the purified enzyme on water permeability was tested in the isolated toad urinary bladder. Water flow through the membrane was measured gravimetrically in bag preparations of the bladder. ACL-I PLA2 (20 nM) did not significantly alter the water permeability in the bladder preparations, whereas ACL myotoxin (ACLMT), a Lys49 PLA2 isolated from the same venom, at similar concentration significantly increased (81%) the water permeability. However, both toxins inhibited the AVP-stimulated water permeability. These results strongly suggest that PLA2 activity is not involved in the ACLMT effect on water transport and the effect of ACL-I PLA2 myotoxin on membrane permeability is mediated by mechanisms that are different in comparison to ACLMT.

摘要

通过凝胶过滤和阳离子交换色谱法从宽带水蛇毒中纯化出一种天冬氨酸49磷脂酶A2(ACL-I PLA2)。它的相对分子质量为14,000,其N端序列与其他蛇毒磷脂酶A2的同源性超过65%。分别以0.3和1.6 mg/kg的剂量将ACL-I PLA2注射到大鼠和小鼠的胫前肌中,注射后3小时和48小时可诱导肌纤维坏死、细胞浸润和水肿。在离体蟾蜍膀胱中测试了纯化酶对水通透性的影响。通过膀胱袋状制剂重量法测量通过膜的水流量。ACL-I PLA2(20 nM)对膀胱制剂中的水通透性没有显著影响,而从相同毒液中分离出的赖氨酸49磷脂酶A2(ACLMT),在相似浓度下可显著提高(81%)水通透性。然而,两种毒素均抑制抗利尿激素刺激的水通透性。这些结果有力地表明,磷脂酶A2活性不参与ACLMT对水转运的作用,并且ACL-I PLA2肌毒素对膜通透性的作用是由与ACLMT不同的机制介导的。

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