Mediratta P K, Das N, Gupta V S, Sen P
Department of Pharmacology, University College of Medical Sciences, New Delhi, India.
NIDA Res Monogr. 1988;87:209-16.
Possible involvement of endogenous opioids in humoral immune responses has been explored in the experimental animals. Opioid agonists like morphine and leu-enkephalin significantly enhanced antigen-induced histamine release from the peritoneal mast cells of sensitised rats in vitro; this was effectively antagonised by naloxone. Naloxone itself inhibited antigen-induced histamine release. Animals were effectively protected against anaphylactic shock by naloxone which also antagonised morphine-induced increase in anaphylactic mortality. Naloxone reduced haemagglutination titre to sheep red blood cells and IgE antibody titre as measured by passive cutaneous anaphylaxis. Thus, endogenous opioids appear to be involved in the mediation of humoral immune responses. They seem to act at various steps in the immune mechanism viz (i) antibody production and (ii) release of mediators of hypersensitivity reactions.
内源性阿片类物质在体液免疫反应中的可能作用已在实验动物中进行了研究。吗啡和亮氨酸脑啡肽等阿片类激动剂在体外显著增强了致敏大鼠腹膜肥大细胞抗原诱导的组胺释放;纳洛酮可有效拮抗这一作用。纳洛酮本身也抑制抗原诱导的组胺释放。纳洛酮可有效保护动物免受过敏性休克,它还能拮抗吗啡诱导的过敏性死亡率增加。通过被动皮肤过敏反应测定,纳洛酮降低了对绵羊红细胞的血凝滴度和IgE抗体滴度。因此,内源性阿片类物质似乎参与了体液免疫反应的介导。它们似乎在免疫机制的各个步骤发挥作用,即(i)抗体产生和(ii)过敏反应介质的释放。