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多巴胺受体 D1 介导了多巴胺对远端结肠运动的抑制作用。

Dopamine receptor D1 mediates the inhibition of dopamine on the distal colonic motility.

机构信息

Department of Physiology and Center of Bioartificial Liver, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.

出版信息

Transl Res. 2012 May;159(5):407-14. doi: 10.1016/j.trsl.2012.01.002. Epub 2012 Jan 27.

Abstract

The motility of distal colon could be inhibited by dopamine (DA), yet, the involved receptor is controversial according to the published reports. The goal of present study was to investigate DA receptor(s) mediated inhibition of DA on the colonic motility in rat. The contraction of isolated colon strips was assessed through isometric force transducer. The expressions of DA receptors in distal colon were detected through immunofluorescence and Western blot. DA concentration in colonic smooth muscle was measured by liquid chromatography/mass spectrometry. The results showed that DA inhibited the spontaneous motility of distal colon in a dose-dependent manner with EC50 8.3 μM. Tetrodotoxin increased colonic contractive frequency, but failed to affect the inhibition of DA on the colonic motility. Pretreatment with SCH-23390, an antagonist of dopaminergic receptor D1, shifted the dose-response curve to the right with EC50 of DA 37 μM. However, blocking dopaminergic receptor D2 with sulpiride, had no effect. The immunoreactivity of D1 and D2 were detected in the distal colon including myenteric plexus and smooth muscle. Acute cold-restraint stress (CRS) enhanced spontaneous contraction of rat distal colon, which was more sensitive to DA compared with control. Moreover, DA content and D1 expression in smooth muscle layer were increased under CRS condition. In conclusion, D1 in the smooth muscle is mediated DA inhibition on the spontaneous contraction of rat distal colon. The increased DA content and D1 receptor expression in the smooth muscle layer could be a compensatory effect under CRS condition to balance the enhanced colonic motility.

摘要

多巴胺(DA)可抑制远端结肠的蠕动,但根据已发表的报道,涉及的受体存在争议。本研究旨在探讨 DA 受体介导的 DA 对大鼠结肠运动的抑制作用。通过等长力换能器评估分离结肠条的收缩。通过免疫荧光和 Western blot 检测远端结肠中 DA 受体的表达。通过液相色谱/质谱法测量结肠平滑肌中的 DA 浓度。结果表明,DA 呈浓度依赖性抑制远端结肠的自发性蠕动,EC50 为 8.3 μM。河豚毒素增加结肠收缩频率,但不能影响 DA 对结肠运动的抑制作用。用 DA 的拮抗剂 SCH-23390 预处理,将 DA 的剂量-反应曲线右移,EC50 为 37 μM。然而,用 D2 受体拮抗剂舒必利阻断 D2 受体没有效果。D1 和 D2 受体在包括肌间神经丛和平滑肌在内的远端结肠中均有免疫反应性。急性冷束缚应激(CRS)增强了大鼠远端结肠的自发性收缩,与对照组相比,对 DA 的敏感性更高。此外,在 CRS 条件下,平滑肌层中的 DA 含量和 D1 表达增加。总之,平滑肌中的 D1 介导了 DA 对大鼠远端结肠自发性收缩的抑制作用。在 CRS 条件下,平滑肌层中 DA 含量和 D1 受体表达的增加可能是一种代偿性反应,以平衡增强的结肠运动。

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