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α1 - 肾上腺素能受体mRNA水平在兔主动脉平滑肌细胞中受去甲肾上腺素调节。

Alpha 1-adrenergic receptor mRNA level is regulated by norepinephrine in rabbit aortic smooth muscle cells.

作者信息

Izzo N J, Seidman C E, Collins S, Colucci W S

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, MA.

出版信息

Proc Natl Acad Sci U S A. 1990 Aug;87(16):6268-71. doi: 10.1073/pnas.87.16.6268.

Abstract

Prolonged agonist exposure results in a decrease in the density of alpha 1-adrenergic receptors in rabbit aortic smooth muscle cells. A cDNA for the alpha 1-adrenergic receptor was used to assess the effect of norepinephrine on alpha 1-adrenergic receptor mRNA level in cultured vascular smooth muscle cells from the rabbit aorta. Norepinephrine caused a transient decrease (81% +/- 5%; n = 9) in alpha 1-adrenergic receptor mRNA. The effect was concentration dependent (EC50, approximately 0.3 microM; maximal effect, 10 microM). The maximum decrease occurred after 4 hr of exposure to norepinephrine and was followed by a gradual return to control levels by 24 hr. The decrease in mRNA level was blocked by prazosin, but not propranolol, and was mimicked by phenylephrine. These results indicate that the effect is mediated by stimulation of the alpha 1-adrenergic receptor and suggest that it involves one or more alpha 1-adrenergic-coupled second messenger pathways. The decrease in alpha 1-adrenergic receptor mRNA caused by norepinephrine exceeds that caused by actinomycin D, suggesting that norepinephrine may cause a decrease in the stability of alpha 1-adrenergic receptor mRNA. Actinomycin D also blocked the norepinephrine-induced decrease in mRNA level, further suggesting that the effect of norepinephrine requires induction of transcription, presumably leading to synthesis of a labile factor that is necessary for the effect of norepinephrine on alpha 1-adrenergic receptor mRNA level.

摘要

长期激动剂暴露导致兔主动脉平滑肌细胞中α1 - 肾上腺素能受体密度降低。使用α1 - 肾上腺素能受体的cDNA来评估去甲肾上腺素对来自兔主动脉的培养血管平滑肌细胞中α1 - 肾上腺素能受体mRNA水平的影响。去甲肾上腺素导致α1 - 肾上腺素能受体mRNA瞬时降低(81%±5%;n = 9)。该效应呈浓度依赖性(EC50约为0.3 microM;最大效应为10 microM)。最大降低在暴露于去甲肾上腺素4小时后出现,随后在24小时内逐渐恢复至对照水平。mRNA水平的降低被哌唑嗪阻断,但未被普萘洛尔阻断,且去氧肾上腺素可模拟该效应。这些结果表明该效应是由α1 - 肾上腺素能受体的刺激介导的,并提示其涉及一条或多条α1 - 肾上腺素能偶联的第二信使途径。去甲肾上腺素引起的α1 - 肾上腺素能受体mRNA降低超过放线菌素D引起的降低,这表明去甲肾上腺素可能导致α1 - 肾上腺素能受体mRNA稳定性降低。放线菌素D也阻断了去甲肾上腺素诱导的mRNA水平降低,进一步表明去甲肾上腺素的作用需要转录诱导,推测这会导致合成一种不稳定因子,该因子对于去甲肾上腺素对α1 - 肾上腺素能受体mRNA水平的作用是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d16/54514/c8e8c66ebd83/pnas01041-0270-a.jpg

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