Samii S I, Webb R A
Department of Biology, York University, Ontario, Canada.
Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1996 Mar;113(3):409-20. doi: 10.1016/0742-8413(96)00007-2.
The effects of L-glutamate, acetylcholine, and serotonin (5HT) were examined on generation of inositol 1,4,5-triphosphate [Ins(1,4,5)P3], in membrane preparations of the cestode Hymenolepis diminuta. Only L-glutamate and acetylcholine stimulated a significant elevation in Ins(1,4,5)P3. The response to L-glutamate was stereospecific; D-glutamate or L-aspartate were not as potent. A role for G-protein(s) was supported by the observations that sodium fluoride stimulated Ins(1,4,5)P3 generation, and the L-glutamate response was potentiated by GTP and GTP-S and was suppressed by GDPS. However, studies with pertussis and cholera toxins indicated that the putative G-protein(s) was not pertussis or cholera toxin sensitive. The pharmacological profile of the L-glutamate response was examined partially. Trans-ACPD was a very effective agonist at 10(-5)M. While 10(-3)M L-glutamate, NMDA, and AMPA significantly elevated Ins(1,4,5)P3 levels, quisqualate and kainate did not. The elevation of Ins(1,4,5)P3 levels by L-glutamate and NMDA was antagonized by the specific glutamatergic antagonists AP-5, AP-7, CNQX, and CPP. While the response to ACPD was antagonized by AP5, CPP and CPG, CNQX was without effect. Collectively, the data support the hypothesis that in the cestode H. diminuta, L-glutamate activation of a metabotropic (ACPD) and/or ionotropic-like AMPA/NMDA receptor subtypes proceeds via a G protein(s) to enhance phospholipase C activity, ultimately resulting in the elevation of Ins(1,4,5)P3 levels in the tissues.
研究了L-谷氨酸、乙酰胆碱和5-羟色胺(5HT)对微小膜壳绦虫膜制剂中肌醇1,4,5-三磷酸[Ins(1,4,5)P3]生成的影响。只有L-谷氨酸和乙酰胆碱能显著刺激Ins(1,4,5)P3升高。对L-谷氨酸的反应具有立体特异性;D-谷氨酸或L-天冬氨酸的作用不强。氟化钠能刺激Ins(1,4,5)P3生成,L-谷氨酸反应被GTP和GTP-S增强而被GDPS抑制,这些观察结果支持了G蛋白发挥作用的观点。然而,百日咳毒素和霍乱毒素研究表明,假定的G蛋白对百日咳毒素或霍乱毒素不敏感。对L-谷氨酸反应的药理学特征进行了部分研究。反式-ACPD在10(-5)M时是一种非常有效的激动剂。虽然10(-3)M的L-谷氨酸、NMDA和AMPA能显著提高Ins(1,4,5)P3水平,但quisqualate和kainate却不能。L-谷氨酸和NMDA引起的Ins(1,4,5)P3水平升高被特异性谷氨酸能拮抗剂AP-5、AP-7、CNQX和CPP拮抗。虽然对ACPD的反应被AP5、CPP和CPG拮抗,但CNQX没有作用。总体而言,这些数据支持以下假设:在微小膜壳绦虫中,代谢型(ACPD)和/或离子型AMPA/NMDA受体亚型的L-谷氨酸激活通过G蛋白增强磷脂酶C活性,最终导致组织中Ins(1,4,5)P3水平升高。