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阿扑吗啡对多形核白细胞胞吐作用和代谢爆发的影响。

The effect of apomorphine on exocytosis and metabolic burst of polymorphonuclear leukocytes.

作者信息

Elferink J G

机构信息

Department of Medical Biochemistry, Sylvius Laboratories, University of Leiden, The Netherlands.

出版信息

Br J Pharmacol. 1987 Dec;92(4):909-13. doi: 10.1111/j.1476-5381.1987.tb11397.x.

Abstract

1 In rabbit polymorphonuclear leukocytes (PMNLs) apomorphine at 10-100 microM inhibits fMet-Leu-Phe and A23187-induced exocytosis, and the phorbol myristate acetate- and fMet-Leu-Phe-induced activation of the metabolic burst. The secretory response was not restored by washing the cells after pretreatment with apomorphine. 2 The inhibitory effect of apomorphine was not prevented by the dopamine receptor antagonists haloperidol and pimozide, nor did dopamine itself inhibit fMet-Leu-Phe-induced exocytosis. It therefore seems unlikely that effects are mediated via dopamine receptors. However, sulphydryl reagents reduced the inhibitory effect of apomorphine, suggesting that it may depend upon interaction with susceptible sulphydryl groups, the intactness of which is required for exocytosis and other functions of PMNLs.

摘要
  1. 在兔多形核白细胞(PMNLs)中,10 - 100微摩尔的阿扑吗啡可抑制甲酰甲硫氨酸-亮氨酸-苯丙氨酸(fMet-Leu-Phe)和A23187诱导的胞吐作用,以及佛波酯肉豆蔻酸酯和fMet-Leu-Phe诱导的代谢爆发激活。在用阿扑吗啡预处理后,通过洗涤细胞并不能恢复分泌反应。2. 多巴胺受体拮抗剂氟哌啶醇和匹莫齐特不能阻止阿扑吗啡的抑制作用,多巴胺本身也不抑制fMet-Leu-Phe诱导的胞吐作用。因此,其作用似乎不太可能是通过多巴胺受体介导的。然而,巯基试剂可降低阿扑吗啡的抑制作用,这表明其可能依赖于与敏感巯基的相互作用,而PMNLs的胞吐作用和其他功能需要这些巯基保持完整。

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