首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Rapid decrease in neuropeptide Y gene expression in rat adrenal gland induced by the alpha 2-adrenoceptor agonist clonidine.
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Rapid decrease in neuropeptide Y gene expression in rat adrenal gland induced by the alpha 2-adrenoceptor agonist clonidine.

机译:α2肾上腺素受体激动剂可乐定诱导大鼠肾上腺神经肽Y基因表达迅速下降。

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摘要

1 The mechanism of regulation of the neuropeptide Y (NPY) gene by pharmacological treatment with the alpha 2-adrenenoceptor agonist, clonidine, was investigated by quantitative Northern blot analysis of the effects of this drug on the NPY mRNA levels in rat adrenal gland and medulla oblongata/pons. 2 In the adrenal gland, clonidine-treatment (50 microgram kg-1, s.c., once daily) resulted in decrease in the amount of NPY mRNA to 44 +/- 10% of the control level in 24 h and then its increase to 162 +/- 16% of the control level after 5 days. Concomitant changes in putative NPY pre-mRNA species (7.0 and 3.3 kb) were observed, probably due to changes at the level of NPY gene transcription. 3 The short-term (24 h) effect of clonidine was blocked by yohimbine (5 mg kg-1, i.p., once daily). Yohimbine alone tended to increase the NPY mRNA level after 24h. 4 The recovery/increase in the NPY mRNA level in the adrenal gland after 5 days treatment with clonidine was similar to its increase after treatment with reserpine (0.5 mg kg-1, i.p., once daily). 5 NPY gene expression in the medulla oblongata/pons was not changed by short- or long-term treatment with clonidine. 6 These results suggest that clonidine suppresses NPY gene expression in the adrenal gland, probably at the level of transcription, by activation of the alpha 2-adrenoceptor.
机译:1通过定量Northern印迹分析了该药物对大鼠肾上腺和延髓中NPY mRNA水平的影响,研究了用α2肾上腺素受体激动剂可乐定进行药理处理来调节神经肽Y(NPY)基因的机制。长方形/桥2在肾上腺,可乐定治疗(50微克kg-1,皮下注射,每天一次)导致NPY mRNA量在24小时内降至对照水平的44 +/- 10%,然后增加到162。 5天后达到对照水平的+/- 16%。观察到推定的NPY前mRNA种类(7.0和3.3 kb)的伴随变化,可能是由于NPY基因转录水平的变化。 3育亨宾(5 mg kg-1,腹膜内,每天一次)阻断了可乐定的短期(24小时)作用。 24小时后,仅育亨宾趋于增加NPY mRNA水平。 4使用可乐定治疗5天后,肾上腺NPY mRNA水平的恢复/增加与利血平治疗后的增加(0.5 mg kg-1,腹膜内,每天一次)相似。 5可乐定的短期或长期治疗不会改变延髓/桥中的NPY基因表达。 6这些结果表明,可乐定可通过激活α2-肾上腺素受体来抑制肾上腺NPY基因的表达,可能在转录水平上。

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