Chang E B, Brown D R, Field M, Miller R J
J Pharmacol Exp Ther. 1984 Feb;228(2):364-9.
Diarrhea is a common manifestation of withdrawal from opiates in dependent subjects. This study examined the possibility that this diarrhea results in part from alterations in intestinal fluid transport. Isolated loops of jejunum, ileum and colon were created in morphine-dependent and nondependent rats implanted s.c. with morphine or lactose pellets, respectively. The administration of naltrexone (1 mg/kg s.c.) or its quaternary analog methylnaltrexone (0.01-3 mg/kg i.v.), which does not readily cross the blood-brain barrier, produced a dose-related reduction in fluid absorption from the jejunum and colon of dependent animals only. Similar effects were observed after the i.c.v. injection of quaternary naltrexone (1.0-10 microgram/rat). Both narcotic antagonists, given by any route, produced no change in ileal absorption. Pretreatment with hexamethonium (10 mg/kg i.v.) or atropine (4 mg/kg i.v.) attenuated the antiabsorptive effects of quaternary naltrexone on the jejunum. Serosal addition of naltrexone (10 microM) had no effect on Na or Cl fluxes, short-circuit current or tissue conductance across isolated segments of intestinal mucosa from dependent and nondependent rats. These results indicate that precipitated opiate withdrawal is associated with decreases in jejunal and colonic fluid absorption mediated at sites within both the central nervous system and periphery. Moreover, these effects are not a consequence of a direct opiate action on enterocytes.
腹泻是阿片类药物依赖者戒断时的常见表现。本研究探讨了这种腹泻部分是由肠液转运改变所致的可能性。分别给皮下植入吗啡或乳糖丸剂的吗啡依赖和非依赖大鼠制备空肠、回肠和结肠的分离肠袢。给予纳曲酮(1mg/kg皮下注射)或其不易透过血脑屏障的季铵类似物甲基纳曲酮(0.01 - 3mg/kg静脉注射),仅使依赖动物的空肠和结肠的液体吸收呈剂量相关减少。脑室内注射季铵纳曲酮(1.0 - 10μg/大鼠)后也观察到类似效应。无论通过何种途径给予这两种麻醉拮抗剂,回肠吸收均无变化。六甲铵(10mg/kg静脉注射)或阿托品(4mg/kg静脉注射)预处理减弱了季铵纳曲酮对空肠的抗吸收作用。在依赖和非依赖大鼠的离体肠黏膜段,浆膜面添加纳曲酮(10μM)对钠或氯通量、短路电流或组织电导均无影响。这些结果表明,阿片类药物戒断所致腹泻与中枢神经系统和外周部位介导的空肠和结肠液体吸收减少有关。此外,这些效应并非阿片类药物对肠上皮细胞直接作用的结果。