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川芎嗪对Ca^(2+)促进的儿茶酚胺分泌抑制效应的研究 被引量:1

A PRELIMINARY STUDY ON THE INHIBITORY ACTION OF LIGUSTRAZINE UPONTHE CATACHOLAMINES RELEASE VOKED BY Ca ̄(2+)
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摘要 用胶原酶分离豚鼠肾上腺髓质嗜铬细胞,获得离体豚鼠肾上腺髓质嗜铬细胞悬液,可用作刺激-分泌偶联研究的模型.2.2mmol/LCa2+促进嗜铬细胞儿茶酚胺的分泌,与无钙组比较有显著差异,不同浓度的川芎嗪(10-2~10-7mol/L)与Ca2+(2.2mmol/L)的混合液作用于细胞悬液,细胞儿茶酚胺的分泌受混合液中Ca2+的促进,而川芎嗪无显著影响.在细胞悬液中,加入川芎嗪(10-3~10-9mol/L)5min后,再加入Ca2+(2.2mmol/L)作用5min,Ca2+对嗜铬细胞儿茶酚胺分泌的促进作用受到抑制,其中川芎嗪浓度为10-6mol/L时,抑制作用最为明显. Guinea pig adrenal gland chromaffin cells were isolated by collagenase(mg/mL) digestion.After a short time (5  ̄ 8 hours) cultivation in buffer Ⅱcontaining 5 mg/mL bovine serum ablumin, chromaffin cell suspensions wereobtained and could be used as the model of stimulus-secretion eoupling.2. 2 mmol/L Ca2+ stimulates the releasing of catecholamine of chromaffin cells.Comparing with free Ca2+, the difference is significance: t= 26. 76>t30,0.01= 2. 75.Cell suspensions were mixed with Ligustrazine (10-2 mol/L ̄10-7 mol/L) and Ca2+(2. 2 mmol/L), release of catecholamine evoked by Ca2+, were not affected byLigustrazine. After cell suspensions were mixed with Ligustrazine (10-3 mol/L10-9 mol/L) 5 minutes, then mixed with Ca2+ (2. 2 mmol/L) 5 minutes, thecatecholamine release evoked by Ca2+ is inhibited by Ligustrazine. WhenLigustrazine concentration is 10-6 mol/L, the inhibitory action is more obvious.
出处 《华中师范大学学报(自然科学版)》 CAS CSCD 1995年第4期489-493,共5页 Journal of Central China Normal University:Natural Sciences
关键词 嗜铬细胞 川芎嗪 儿茶酚胺 分泌 抑制效应 Guinea pig adrenomedullary chromaffin cell Ca ̄(2+) Ligustrazine stimulus-secretion coupling
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