幽门结扎、低温约束应激、阿司匹林、吲哚美辛、利血平对吗啡依赖大鼠胃致孕作用的研究。

Alcohol and drug research Pub Date : 1987-01-01
N S Parmar, M Tariq, A M Ageel
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引用次数: 0

摘要

研究了吗啡依赖大鼠幽门结扎6 h、低温约束应激、阿司匹林、吲哚美辛、利血平对胃黏膜的损伤。在饮用水中逐渐增加硫酸吗啡浓度21 ~ 24 d后产生吗啡耐受和依赖。吗啡产生的耐受性和依赖性分别通过热板试验中吗啡镇痛反应降低和产生纳洛酮沉淀戒断综合征来证实。吗啡依赖大鼠幽门结扎、阿司匹林和吲哚美辛对胃粘膜的损伤程度明显高于未用药大鼠。对胃液的研究未发现结扎6 h大鼠胃液量、可滴定酸度和胃输出量有明显变化。利血平治疗和低温抑制应激大鼠的平均病变评分与未用药大鼠无显著差异。需要进一步的研究来确定这些观察结果背后的确切机制。
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Studies on the gastroulcerogenic effects of pylorus ligation, hypothermic restraint stress, aspirin, indomethacin and reserpine in morphine dependent rats.

The gastric mucosal damage induced by pylorus ligation for 6 h, hypothermic restraint stress, aspirin, indomethacin and reserpine was studied in morphine dependent rats. Morphine tolerance and dependence were produced by administering the gradually increasing concentrations of morphine sulphate in drinking water for 21-24 days. The tolerance and dependence produced by morphine were confirmed by a decreased analgesic response to morphine in the hot plate test and by producing a naloxone precipitated withdrawal syndrome respectively. The intensity of gastric mucosal damage induced by pylorus ligation, aspirin and indomethacin was significantly higher in morphine dependent rats than that observed in the naive animals. Studies on the gastric secretion did not reveal any significant change in the volume of gastric secretion, titrable acidity and gastric output of 6 h pylorus ligated rats. The average lesion scores in the reserpine treated and hypothermic restraint stressed rats were not significantly different from those obtained in the naive animals. Further studies are required to establish the exact mechanisms underlying these observations.

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Cyclo (Leu-Gly) attenuates the striatal dopaminergic supersensitivity induced by chronic morphine. Alcohol preference and regional brain monoamine contents of N/Nih heterogeneous stock rats. Toxicity of MDA (3,4-methylenedioxyamphetamine) considered for relevance to hazards of MDMA (Ecstasy) abuse. Alprazolam dependence in mice. Chronic cocaine administration induces opposite changes in dopamine receptors in the striatum and nucleus accumbens.
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