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Antinociceptive effect of MAS MT in rats.

机译:MAS MT在大鼠中的抗伤害感受作用。

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摘要

MAS MT is a myotropic decapeptide isolated from Manduca sexta. This peptide exerts stimulatory effect on the heart-beat frequency of insects. The present study was conducted to determine a probable antinociceptive effect in rats of a native synthetic decapeptide, MAS MT-I, and its 2 analogues, heptapeptides MAS MT-II and MAS MT-III. All these peptides were applied directly into the lateral brain ventricle (icv) at 3 doses: 10, 25 and 50 nmol. The analgesic (antinociceptive) effect was evaluated by a tail immersion test. It was found that 25 and 50 nmol of MAS MT-I induced significant antinociceptive effect, while MAS MT-II and MAS MT-III exerted a less antinociceptive effect in comparison with native MAS MT-I. Prior icv administration of naloxone, an opioid antagonist, weakly blocked the MAS MT-I effect. It is concluded that the antinociceptive effect of MAS MT-I in rats is not mediated by the central opioid system.
机译:MAS MT是一种从曼杜卡六倍体中分离出来的肌肽十肽。该肽对昆虫的心跳频率具有刺激作用。进行本研究是为了确定天然合成的十肽MAS MT-I及其2种类似物七肽MAS MT-II和MAS MT-III在大鼠中的可能的抗伤害作用。所有这些肽均以10、25和50 nmol的3种剂量直接应用于脑外侧脑室(icv)。通过尾部浸入试验评价镇痛(镇痛)作用。已经发现,与天然MAS MT-1相比,MAS MT-1的25和50nmol诱导了显着的抗伤害感受作用,而MAS MT-II和MAS MT-III的抗伤害感受作用较小。先前的icv给予阿片样物质拮抗剂纳洛酮微弱地阻断了MAS MT-1的作用。结论是,MAS MT-1对大鼠的镇痛作用不是由中央阿片样物质系统介导的。

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