首页> 外文期刊>The Journal of Physiology >Tetrahydrobiopterin regulates cyclic GMP-dependent electrogenic Cl- secretion in mouse ileum in vitro.
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Tetrahydrobiopterin regulates cyclic GMP-dependent electrogenic Cl- secretion in mouse ileum in vitro.

机译:四氢生物蝶呤在体外调节小鼠回肠中依赖于循环GMP的基因型Cl分泌。

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1. Basal electrogenic Cl- secretion, measured as the short-circuit current (Isc), was variable in ileum removed from tetrahydrobiopterin (BH4)-deficient hph-1 mice and wild-type controls in vitro, although values were not significantly different. 2. The basal nitrite release and mucosal cyclic guanosine 3',5'-monophosphate (cyclic GMP) production were similar in control and BH4-deficient ileum. 3. Mucosally added Escherichia coli heat-stable toxin (STa, 55 ng ml-1) increased the nitrite release, cyclic GMP levels and the Isc in control ileum, but its secretory actions were reduced in BH4-deficient ileum. 4. L-Arginine (1 mM) increased the nitrite release, cyclic GMP production and the Isc in control ileum, but the actions were reduced in BH4-deficient ileum. 5. Serosal carbachol (1 mM) stimulated maximum short-circuit currents of similar magnitude in both control and BH4-deficient ileum, whilst nitrite release and cyclic GMP production were minimal. 6. E. coli STa and L-arginine increased electrogenic Cl- secretion across intact mouse ileum in vitro by releasing nitric oxide and elevating mucosal cyclic GMP. The inhibition of these processes in the hph-1 mouse ileum suggests that BH4 may be a target for the modulation of electrogenic transport, and highlight the complexity of the interactions between nitric oxide and cyclic GMP in the gut.
机译:1.以短路电流(Isc)衡量的基础上电的Cl分泌在体外从四氢生物蝶呤(BH4)缺陷型hph-1小鼠和野生型对照中去除的回肠中是可变的,尽管其值没有显着差异。 2.在对照和缺乏BH4的回肠中,基底亚硝酸盐的释放和粘膜环状鸟苷3',5'-单磷酸盐(环状GMP)的产生相似。 3.粘膜添加的大肠杆菌热稳定毒素(STa,55 ng ml-1)增加了控制回肠中的亚硝酸盐释放,循环GMP水平和Isc,但在BH4缺乏回肠中其分泌作用降低了。 4. L-精氨酸(1 mM)增加了控制回肠中亚硝酸盐的释放,循环GMP的产生和Isc,但在缺乏BH4的回肠中的作用减少了。 5.在对照和缺乏BH4的回肠中,浆膜碳酰胆碱(1 mM)刺激了最大的相似大小的短路电流,而亚硝酸盐的释放和循环GMP的产生却最小。 6.大肠杆菌STa和L-精氨酸可通过释放一氧化氮和升高粘膜环状GMP来增加完整小鼠回肠的电化学Cl分泌。在hph-1小鼠回肠中对这些过程的抑制表明BH4可能是调节电运输的靶标,并突显了肠道中一氧化氮与环状GMP之间相互作用的复杂性。

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