Presynaptic α-2C adrenoceptor-mediated control of noradrenaline release in humans:: Genotype- or age-dependent?

被引:6
作者
Bruck, H.
Schwerdtfeger, T.
Toliat, M.
Leineweber, K.
Heusch, G.
Philipp, T.
Nuernberg, P.
Brodde, O-E [1 ]
机构
[1] Univ Essen Gesamthsch, Sch Med, Dept Nephrol, Essen, Germany
[2] Univ Cologne, Cologne Ctr Genom, Cologne, Germany
[3] Univ Essen Gesamthsch, Sch Med, Dept Pathophysiol, Essen, Germany
关键词
D O I
10.1038/sj.clpt.6100181
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In vitro alpha-2CDel322-325 adrenoceptor (AR) polymorphism exhibits reduced functional responsiveness. We studied whether this is true also in vivo in humans. We assessed in nine young wild-type (WT) alpha-2C AR subjects (aged 23 years), 10 elder WT alpha-2C AR subjects (aged 63 years), and nine alpha-2CDel AR subjects (aged 28 years) clonidine (1 mu g/kg intravenous (i. v.) bolus)-evoked plasma noradrenaline (pNA), heart rate (HR), and blood pressure (BP) changes. Clonidine-evoked pNA decreases were comparable in young WT alpha-2C and in alpha-2CDel AR subjects, but significantly lower (P = 0.033) in elder subjects. Similarly, clonidine-evoked HR decreases were significantly larger in young WT alpha-2C and in alpha-2CDel AR subjects than in elder subjects, whereas clonidine-evoked BP decreases were larger in elder subjects. In conclusion, alpha-2CDel AR appears to play only a minor role in presynaptic regulation of NA release and/ or to be not hypofunctional in vivo in humans, but functional responsiveness of presynaptic alpha-2 AR declines with ageing.
引用
收藏
页码:525 / 530
页数:6
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