首页> 外文期刊>European Journal of Pharmacology: An International Journal >Cross-tolerance and convergent dependence between morphine and cannabimimetic agent WIN 55,212-2 in the guinea-pig ileum myenteric plexus.
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Cross-tolerance and convergent dependence between morphine and cannabimimetic agent WIN 55,212-2 in the guinea-pig ileum myenteric plexus.

机译:吗啡与大麻模拟剂WIN 55,212-2在豚鼠回肠肌层神经丛中的交叉耐受和会聚依赖性。

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摘要

The cross-tolerance and convergent dependence between morphine and the cannabimimetic agent R(+)-[2,3-dihydro-5-methyl-3[(morpholinyl)methyl]pyrrolo[1,2,3-de]-1,4-+ ++benzoxazin-yl]-(1-naphthalenyl) methanone mesylate (WIN 55,212-2) were assessed in vitro on guinea-pig ileum. To induce tolerance and dependence the myenteric plexus-longitudinal muscle was incubated at 37 degrees C for 5 h with a fixed concentration representing the IC50 for each compound. Myenteric plexus-longitudinal muscle exposed to WIN 55,212-2 (5 x 10(-8) M) was less sensitive to its inhibitory effect on electrically evoked contractions than naive myenteric plexus-longitudinal muscle. The exposure to cannabinoid induced a parallel rightward shift in the lower part of the concentration-response curve of WIN 55,212-2 and a marked reduction in the maximal inhibitory effect of the drug. Myenteric plexus-longitudinal muscle tolerant to WIN 55,212-2 was subsensitive to the inhibitory effect of morphine on the twitch response. The cross-tolerance between WIN 55,212-2 and morphine was bidirectional. In fact, after 5 h the morphine (10(-7) M)-incubated myenteric plexus-longitudinal muscle was less sensitive to the inhibitory effect of WIN 55,212-2. The tissue tolerant to morphine or WIN 55,212-2 was tested for the presence of physical dependence. Naloxone (10(-5) M) produced a typical withdrawal contracture in morphine-tolerant myenteric plexus-longitudinal muscle which could be reduced by a 15-min pretreatment with WIN 55,212-2 (5 X 10(-8) M). In contrast, SR141716 (10(-6) M) [N-(piperidino)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-3-pyr azole-carboxamide], a concentration which fully antagonized the inhibitory effect of WIN 55,212-2 (10(-7) M) in control preparations, did not produce significant contracture in WIN 55,212-2-tolerant myenteric plexus-longitudinal muscle. The mechanisms underlying the cross-tolerance and convergent dependence remain to be ascertained.
机译:吗啡与大麻模拟剂R(+)-[2,3-二氢-5-甲基-3 [(吗啉基)甲基]吡咯并[1,2,3-de] -1,4之间的交叉耐受性和收敛依赖性在豚鼠回肠上体外评估甲磺酸甲磺酸酯+-++苯并恶嗪-基]-(1-萘基)甲磺酸甲酯(WIN 55,212-2)。为了诱导耐受性和依赖性,将肌间神经丛-纵肌在37℃下以代表每种化合物的IC 50的固定浓度孵育5小时。暴露于WIN 55,212-2(5 x 10(-8)M)的肌间神经丛纵肌对其对电诱发收缩的抑制作用不如幼稚的肌间神经丛纵肌。暴露于大麻素会在WIN 55,212-2的浓度-反应曲线的下部引起平行的向右移动,并显着降低药物的最大抑制作用。耐WIN 55,212-2的肌间神经丛纵向肌肉对吗啡对抽搐反应的抑制作用不敏感。 WIN 55,212-2和吗啡之间的交叉耐受性是双向的。实际上,在5小时后,吗啡(10(-7)M)培养的肌间神经丛纵向肌肉对WIN 55,212-2的抑制作用较不敏感。测试了对吗啡或WIN 55,212-2耐受的组织是否存在物理依赖性。纳洛酮(10(-5)M)在耐吗啡的肌间神经丛纵向肌中产生典型的缩回挛缩,可通过WIN 55,212-2(5 X 10(-8)M)预处理15分钟来减少。相反,SR141716(10(-6)M)[N-(哌啶子基)-5-(4-氯苯基)-1-(2,4-二氯苯基)-4-甲基-3-吡唑-羧酰胺]完全拮抗WIN 55,212-2(10(-7)M)在对照制剂中的抑制作用的浓度,在WIN 55,212-2耐受的肌间神经丛-纵肌中不会产生明显的挛缩。交叉容差和收敛依赖性的基础机制尚待确定。

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