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BC3H1非融合肌细胞系的肾上腺素能受体和胆碱能受体药理学

Pharmacology of the adrenoceptors and cholinoceptors of the BC3H1 nonfusing muscle cell line.

作者信息

Mauger J P, Moura A M, Worcel M

出版信息

Br J Pharmacol. 1978 Sep;64(1):29-36. doi: 10.1111/j.1476-5381.1978.tb08637.x.

Abstract
  1. We have studied the action of different transmitters on the transmembrane 42K or 86Rb efflux from tissue cultures of the BC3H1 muscle cell line. 2. The effect of catecholamines and carbachol (CCh) on the isotope efflux rate was measured by addition of the drugs at different times during the washout. 3. Noradrenaline (NA), phenylephrine (Phe), isoprenaline (Iso) and CCh increased 42K and 86Rb efflux rate in a dose-dependent manner. 4. The action of NA seems to be due exclusively to the stimulation of alpha-receptors, since its effect was blocked by phentolamine but not by propranolol. The effects of Iso on the 86Rb efflux were inhibited by propranolol. The beta-receptors in the BC3H1 cells seem to be the beta2-type since they are stimulated by Iso and insensitive to NA. 5. The effect of CCh was blocked (+)-tubocurarine but not by atropine. This result confirms the presence of nicotinic receptors in BC3H1 cells.
摘要
  1. 我们研究了不同递质对BC3H1肌肉细胞系组织培养物中42K或86Rb跨膜外流的作用。2. 在洗脱过程中的不同时间添加药物,测量儿茶酚胺和卡巴胆碱(CCh)对同位素外流速率的影响。3. 去甲肾上腺素(NA)、苯肾上腺素(Phe)、异丙肾上腺素(Iso)和CCh以剂量依赖性方式增加42K和86Rb外流速率。4. NA的作用似乎完全是由于α受体的刺激,因为其作用被酚妥拉明阻断,而未被普萘洛尔阻断。Iso对86Rb外流的作用被普萘洛尔抑制。BC3H1细胞中的β受体似乎是β2型,因为它们受Iso刺激且对NA不敏感。5. CCh的作用被(+)-筒箭毒碱阻断,但未被阿托品阻断。该结果证实了BC3H1细胞中存在烟碱受体。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aacf/1668255/41fe3ae65ea0/brjpharm00428-0033-a.jpg

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