Djurić V J, Wang L, Bienenstock J, Perdue M H
Department of Pathology, Faculty of Health Science, McMaster University, Hamilton, Ontario, Canada.
Brain Behav Immun. 1995 Jun;9(2):87-100. doi: 10.1006/brbi.1995.1010.
Following sensitization to ovalbumin (OA), male Wistar rats were pretreated with naloxone (20 mg/kg i.p.) and subjected to antigen challenge (3 mg OA i.p.). Naloxone exacerbated both systemic and intestinal anaphylaxis when injected 10 and 90 min before the antigen challenge. This was evidenced by a more pronounced drop in rectal temperature, higher hematocrit values, and by an enhanced elevation of basal short-circuit current (an indication of the secretory tone of the small intestine studied in Ussing chambers). Pretreatment with an equipotent does of methylnaloxone (200 mg/kg i.p.), a peripherally acting opiate antagonist, exacerbated the indices of intestinal anaphylaxis but had no apparent effect on indices of systemic anaphylaxis. Thus, our data strongly suggest that in the rat, components of the systemic hypersensitivity reaction are mediated through central opioid receptors, whereas the changes in gut function characterizing intestinal anaphylaxis are mediated through peripheral opioid receptors.
对卵清蛋白(OA)致敏后,雄性Wistar大鼠用纳洛酮(20mg/kg腹腔注射)进行预处理,然后接受抗原攻击(3mg OA腹腔注射)。当在抗原攻击前10分钟和90分钟注射时,纳洛酮加剧了全身和肠道过敏反应。这表现为直肠温度更明显下降、血细胞比容值更高,以及基础短路电流升高增强(这是在尤斯灌流小室中研究的小肠分泌张力的一个指标)。用等效剂量的甲基纳洛酮(200mg/kg腹腔注射)进行预处理,甲基纳洛酮是一种外周作用的阿片类拮抗剂,加剧了肠道过敏反应指标,但对全身过敏反应指标没有明显影响。因此,我们的数据强烈表明,在大鼠中,全身过敏反应的成分是通过中枢阿片受体介导的,而表征肠道过敏反应的肠道功能变化是通过外周阿片受体介导的。