Nath C, Gulati A, Dhawan K N, Gupta G P
Department of Pharmacology & Therapeutics, K.G.'s Medical College, Lucknow, India.
Life Sci. 1988;42(24):2413-7. doi: 10.1016/0024-3205(88)90339-6.
The role of the central histaminergic system in depression was studied by using swimming despair test in mice - a behavioural model of depression. In this test, immobility of mice reflects a state of depression. Intracerebral (ic) injection of histamine (50-200 micrograms) increased significantly the immobility. The H1-receptor blocker mepyramine (2.5-20 mg/kg ip) had no effect while H2-receptor blocker cimetidine (100-200 micrograms ic) caused a significant decrease in immobility. The histamine induced facilitation was blocked completely by cimetidine and antidepressant drugs-imipramine and desipramine, but remained unaffected in mice pretreated with mepyramine or atropine. The H2 agonist impromidine (20-40 micrograms ic) also enhanced significantly, the immobility which was blocked by cimetidine and antidepressant drugs. It has been concluded that central H2-receptors facilitate depression and antidepressant drugs block central H2-receptors.
通过在小鼠中使用游泳绝望试验(一种抑郁症行为模型)来研究中枢组胺能系统在抑郁症中的作用。在该试验中,小鼠的不动反映了抑郁状态。脑内注射组胺(50 - 200微克)显著增加了不动时间。H1受体阻滞剂美吡拉敏(2.5 - 20毫克/千克,腹腔注射)没有效果,而H2受体阻滞剂西咪替丁(100 - 200微克,脑内注射)使不动时间显著减少。组胺诱导的促进作用被西咪替丁和抗抑郁药物丙咪嗪及地昔帕明完全阻断,但在用美吡拉敏或阿托品预处理的小鼠中不受影响。H2激动剂英普咪定(20 - 40微克,脑内注射)也显著增强了不动时间,这被西咪替丁和抗抑郁药物阻断。得出的结论是,中枢H2受体促进抑郁,而抗抑郁药物阻断中枢H2受体。