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Interplay of Hydrogen Sulfide and Nitric Oxide on the Pacemaker Activity of Interstitial Cells of Cajal from Mouse Small Intestine

机译:硫化氢和一氧化氮的相互作用对小鼠小肠Cajal间质细胞起搏器活性的影响

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摘要

We studied whether nitric oxide (NO) and hydrogen sulfide (H2S) have an interaction on the pacemaker activities of interstitial cells of Cajal (ICC) from the mouse small intestine. The actions of NO and H2S on pacemaker activities were investigated by using the whole-cell patch-clamp technique and intracellular Ca2+ analysis at 30℃ in cultured mouse ICC. Exogenously applied (±)-S-nitroso-N-acetylpenicillamine (SNAP), an NO donor, or sodium hydrogen sulfide (NaHS), a donor of H2S, showed no influence on pacemaker activity (potentials and currents) in ICC at low concentrations (10 µM SNAP and 100 µM NaHS), but SNAP or NaHS completely inhibited pacemaker amplitude and pacemaker frequency with increases in the resting currents in the outward direction at high concentrations (SNAP 100 µM and NaHS 1 mM). Co-treatment with 10 µM SNAP plus 100 µM NaHS also inhibited pacemaker amplitude and pacemaker frequency with increases in the resting currents in the outward direction. ODQ, a guanylate cyclase inhibitor, or glibenclamide, an ATP-sensitive K+ channel inhibitor, blocked the SNAP+NaHS-induced inhibition of pacemaker currents in ICC. Also, we found that SNAP+NaHS inhibited the spontaneous intracellular Ca2+ ([Ca2+]i) oscillations in cultured ICC. In conclusion, this study describes the enhanced inhibitory effects of NO plus H2S on ICC in the mouse small intestine. NO+H2S inhibited the pacemaker activity of ICC by modulating intracellular Ca2+. These results may be evidence of a physiological interaction of NO and H2S in ICC for modulating gastrointestinal motility.
机译:我们研究了一氧化氮(NO)和硫化氢(H2S)是否对小鼠小肠Cajal间质细胞(ICC)的起搏器活性具有相互作用。通过全细胞膜片钳技术和培养的小鼠ICC在30℃下的细胞内Ca 2+分析,研究了NO和H 2 S对起搏器活性的作用。外源施用(±)-S-亚硝基-N-乙酰青霉胺(SNAP)(NO供体)或硫化氢钠(NaHS)(H2S供体)在低浓度下对ICC中的起搏器活动(电位和电流)没有影响(10 µM SNAP和100 µM NaHS),但在高浓度(SNAP 100 µM和NaHS 1 mM)下,随着向外静息电流的增加,SNAP或NaHS完全抑制了起搏器幅度和起搏器频率。 10 µM SNAP加100 µM NaHS的共同处理还抑制了起搏器幅度和起搏器频率,同时增加了向外的静息电流。 ODQ(一种鸟苷酸环化酶抑制剂)或glibenclamide(一种ATP敏感的K +通道抑制剂)阻断了SNAP + NaHS对ICC中起搏器电流的抑制作用。此外,我们发现SNAP + NaHS抑制了培养的ICC中自发的细胞内Ca2 +([Ca2 +] i)振荡。总之,这项研究描述了NO加H2S对小鼠小肠ICC的增强抑制作用。 NO + H2S通过调节细胞内Ca2 +抑制ICC的起搏器活性。这些结果可能是ICC中NO和H2S在调节胃肠动力方面的生理相互作用的证据。

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