长期非洲爪蟾蝌蚪心脏器官培养:甲状腺素治疗对蝌蚪心脏胆碱能和肾上腺素能敏感性的生理变化

IF 2.1 Q3 PHYSIOLOGY
Hideki Hanada , Fumihiro Morishita , Seigo Sanoh , Keiko Kashiwagi , Akihiko Kashiwagi
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引用次数: 0

摘要

本研究阐明了用乙酰胆碱(ACh)、去甲肾上腺素(NE)和阿托品暴露于甲状腺素(T4)的培养的Nieuwkoop和Faber 57期非洲爪蟾蝌蚪器官心脏的生理敏感性变化。对于初步寿命和化学测试,制备了60%最低必需培养基(MEM)、两种含有相对较低浓度氨基酸和胶原蛋白的改良Hank’s平衡盐溶液培养基(MHBSS-CM)I和II。在培养的蝌蚪心脏的初步寿命测试中,在60%MEM中维持的心脏平均为50天,而在MHBSS CMs中的蝌蚪心脏平均延长了109天,显示出MHBSS CM的优越性。×10−9 M T4刺激4 min可使蝌蚪心跳加快。10−9 M ACh降低了蝌蚪的心跳。变态完成后2-4周的蛙心和用5×10−10 M T4处理45小时的蝌蚪心也对10−9 M ACh有反应,低静息心脏用竞争性毒蕈碱拮抗剂10−8 M阿托品恢复到对照水平,而过量暴露10−5M阿托品于T4处理的蝌蚪心脏并没有增加心跳,尽管青蛙的心跳比对照组增加。10−14-10−12 M NE以浓度依赖的方式增加蝌蚪的心跳,然而,10−12 M NE对T4处理的蝌蚪和蛙心上的肾上腺素能受体都没有刺激作用。这些结果表明,T4诱导器官培养的蝌蚪心脏中对阿托品敏感的毒蕈碱和肾上腺素能受体的脱敏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term Xenopus laevis tadpole -heart-organ-culture: Physiological changes in cholinergic and adrenergic sensitivities of tadpole heart with thyroxine-treatment

The present study clarified changes in physiological sensitivities of cultured Nieuwkoop and Faber stage 57 Xenopus laevis tadpole-organ-heart exposed to thyroxine (T4) using acetylcholine (ACh), norepinephrine (NE) and atropine. For preliminary life span and the chemical tests, 60% minimum essential medium (MEM), two types of modified Hank's balanced salt-solution-culture-media (MHBSS-CM) I and II containing relatively lower concentrations of amino acids and collagen were prepared. In preliminary lifespan-test of cultured tadpole hearts, the hearts maintained in 60% MEM was 50 days on average, whereas that of the tadpole-hearts in MHBSS-CMs was extended by 109 days on average, showing superior effectiveness of MHBSS-CMs. 4 min-stimulation by 5 × 10−9 M T4 tended to increase the tadpole heartbeat. 10−9 M ACh decreased the tadpole heartbeat. Frog-heart at 2–4 weeks after metamorphosis completion and tadpole heart treated with 5 × 10−10 M T4 for 45 h also responded to 10−9 M ACh, and low-resting hearts were restored to the control level with the competitive muscarinic antagonist 10−8 M atropine, whereas excessive exposure of 10−5 M atropine to T4-treated tadpole heart did not increase heartbeat in spite of the increased frog heartbeat over the control. 10−14 —10−12 M NE increase the tadpole heartbeat in a concentration-dependent manner, however, 10−12 M NE did not act to stimulate adrenergic receptors on both T4-treated tadpole- and the frog-hearts. These results suggest that T4 induces the desensitization of atropine-sensitive muscarinic and adrenergic receptors in organ-cultured tadpole-heart.

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