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激动剂对心脏毒蕈碱受体各组分的影响。

The effects of agonists on the components of the cardiac muscarinic receptor.

作者信息

Burgen A S

机构信息

Department of Pharmacology, University of Cambridge.

出版信息

Br J Pharmacol. 1987 Oct;92(2):327-32. doi: 10.1111/j.1476-5381.1987.tb11327.x.

Abstract

1 The binding of eleven agonists to muscarinic receptors in the rat heart has been measured in competition with [3H]-N-methylscopolamine. 2 Full analysis of binding required the resolution of three components (SH, H and L). 3 The proportion of the H component was independent of agonist structure. The proportion of the SH component ranged from 2-36% of the total and was dependent on the agonist. The proportion of the L component varied in a complementary way from 59-22% of the total. 4 The ratios of the affinities of ten of the agonists to the three components of the receptors were constant; the weakest binding agonist, choline, had lower ratios of affinity. 5 When saturated with guanylylimidodiphosphate (GppNHp) the SH receptor population was no longer detectable and the H receptor population was reduced by 63%: about 85% of the receptors was in the L population. 6 The affinity constants of agonists for the H and L forms of the receptors were not changed by GppNHp. 7 The results are interpreted in terms of the effects of accessory proteins on the proportions of binding and non-binding conformations of the receptor.

摘要
  1. 已通过与[3H]-N-甲基东莨菪碱竞争,测定了11种激动剂与大鼠心脏毒蕈碱受体的结合情况。2. 结合的全面分析需要分辨出三个成分(SH、H和L)。3. H成分的比例与激动剂结构无关。SH成分的比例占总量的2%-36%,且取决于激动剂。L成分的比例则以互补方式从总量的59%-22%变化。4. 十种激动剂与受体三个成分的亲和力比值是恒定的;结合最弱的激动剂胆碱,其亲和力比值较低。5. 当用鸟苷酰亚胺二磷酸(GppNHp)饱和时,SH受体群体不再可检测到,H受体群体减少了63%:约85%的受体处于L群体中。6. GppNHp未改变激动剂对受体H和L形式的亲和力常数。7. 根据辅助蛋白对受体结合和非结合构象比例的影响对结果进行了解释。

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2
Assessment of mechanistic proposals for the binding of agonists to cardiac muscarinic receptors.
Biochemistry. 1986 Nov 4;25(22):6995-7008. doi: 10.1021/bi00370a037.

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4
The character of the muscarinic receptors in different regions of the rat brain.大鼠脑不同区域毒蕈碱受体的特性
Proc R Soc Lond B Biol Sci. 1980 Feb 13;207(1166):1-12. doi: 10.1098/rspb.1980.0011.
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Assessment of mechanistic proposals for the binding of agonists to cardiac muscarinic receptors.
Biochemistry. 1986 Nov 4;25(22):6995-7008. doi: 10.1021/bi00370a037.
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The effect of ionic strength on cardiac muscarinic receptors.离子强度对心肌毒蕈碱受体的影响。
Br J Pharmacol. 1986 Jun;88(2):451-5. doi: 10.1111/j.1476-5381.1986.tb10223.x.

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