Cogo J C, Prado-Franceschi J, Giglio J R, Corrado A P, Cruz-Höfling M A, Donato J L, Leite G B, Rodrigues-Simioni L
Department of Physiology, Institute of Biology, UNICAMP, Campinas, S.P., Brazil.
Toxicon. 1998 Oct;36(10):1323-32. doi: 10.1016/s0041-0101(97)00174-8.
A phospholipase A2-containing fraction was isolated from the venom of Bothrops insularis by a combination of gel filtration on Sephadex G-150 and ion exchange chromatography on DEAE-Sephadex. Peak IV of the latter chromatography containing all of the phospholipase A2 (PLA2) activity, was assayed on isolated neuromuscular preparations. In the mouse phrenic nerve-diaphragm incubated in Tyrode at 37 degrees C, the PLA2 fraction produced an initial increase in the twitch tension and in the frequency of the mepps, followed by a dose-dependent, irreversible blockade. The replacement of 1.8 mM Ca2+ by 4 mM Sr2 inhibited the neuromuscular blocking effect of the fraction. In the chick hiventer cervicis preparation incubated with Krebs solution at 37 degrees C, the PLA2 fraction induced blockade but did not affect the response to acetylcholine and K+, excluding the involvement of post-synaptic and direct muscular effects. A low temperature (18-22 degrees C) incubation prevented the neuromuscular effect from developing. These results suggest that the PLA2-containing fraction acts predominantly at presynaptic sites at the neuromuscular junction. This fraction also accounts for most of the pharmacological effects of the crude venom.
通过在Sephadex G - 150上进行凝胶过滤和在DEAE - Sephadex上进行离子交换色谱相结合的方法,从海岛矛头蝮蛇毒中分离出了一个含磷脂酶A2的组分。后一种色谱的峰IV含有所有的磷脂酶A2(PLA2)活性,对分离出的神经肌肉制剂进行了检测。在37℃下于台氏液中孵育的小鼠膈神经 - 膈肌标本中,PLA2组分最初使抽搐张力和微小终板电位(mepps)频率增加,随后出现剂量依赖性的、不可逆的阻滞。用4 mM Sr2+取代1.8 mM Ca2+可抑制该组分的神经肌肉阻滞作用。在37℃下用克雷布斯溶液孵育的鸡颈静脉标本中,PLA2组分诱导阻滞,但不影响对乙酰胆碱和K+的反应,排除了突触后和直接肌肉效应的参与。低温(18 - 22℃)孵育可阻止神经肌肉效应的产生。这些结果表明,含PLA2的组分主要作用于神经肌肉接头的突触前部位。该组分也解释了粗毒的大部分药理作用。