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内源性阿片肽对体液免疫反应的调节

Modulation of humoral immune responses by endogenous opioids.

作者信息

Mediratta P K, Das N, Gupta V S, Sen P

机构信息

Department of Pharmacology, University College of Medical Sciences, New Delhi, India.

出版信息

J Allergy Clin Immunol. 1988 Jan;81(1):27-32. doi: 10.1016/0091-6749(88)90216-3.

Abstract

The effects of opioid agonists and antagonists were investigated on humoral immune mechanisms in mice and rats. Opioid agonists like morphine, Leu-enkephalin, and Met-enkephalin, enhanced antigen-induced histamine release from mixed peritoneal cells of rats in vitro; this enhancement was effectively antagonized by naloxone, an opioid antagonist. Naloxone, per se, decreased anaphylactic mortality in doses of 10 mg/kg, while it increased mortality in a dose of 1 mg/kg. Reduced IgE antibody titer, measured by passive cutaneous anaphylaxis, decreased hemagglutination titer to sheep red blood cells, blocked histamine release from mixed peritoneal cells of rats in vitro induced by antigen, but had no significant effect when histamine release was induced by compound 48/80. Thus, it appears that endogenous opioids are involved in humoral immune responses.

摘要

研究了阿片类激动剂和拮抗剂对小鼠和大鼠体液免疫机制的影响。吗啡、亮氨酸脑啡肽和甲硫氨酸脑啡肽等阿片类激动剂,在体外增强了抗原诱导的大鼠混合腹膜细胞组胺释放;这种增强作用被阿片类拮抗剂纳洛酮有效拮抗。纳洛酮本身,剂量为10mg/kg时可降低过敏性死亡率,而剂量为1mg/kg时则增加死亡率。通过被动皮肤过敏反应测定的IgE抗体滴度降低,对绵羊红细胞的血凝滴度降低,阻断了体外抗原诱导的大鼠混合腹膜细胞组胺释放,但在由化合物48/80诱导组胺释放时无显著影响。因此,内源性阿片类物质似乎参与了体液免疫反应。

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