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脑血管对高钾的反应——一氧化氮在离体大鼠大脑中动脉体外模型中的作用

The cerebrovascular response to elevated potassium--role of nitric oxide in the in vitro model of isolated rat middle cerebral arteries.

作者信息

Schuh-Hofer S, Lobsien E, Brodowsky R, Vogt J, Dreier J P, Klee R, Dirnagl U, Lindauer U

机构信息

Department of Experimental Neurology, Humboldt University, Charité Hospital, 10098, Berlin, Germany.

出版信息

Neurosci Lett. 2001 Jun 22;306(1-2):61-4. doi: 10.1016/s0304-3940(01)01878-x.

Abstract

We investigated the role of nitric oxide (NO) in the vascular response to high extraluminal K(+)-concentrations in the in vitro model of isolated rat middle cerebral arteries (MCA). Under control conditions, rat MCA dilated at 20, 30, 40 and 60 mM K(+). At 80 mM K(+), a slight vasoconstriction occurred. The unspecific NO synthase (NOS)-inhibitor L(omega)-nitro-L-arginine (L-NNA) increased the resting tone at 3 mM K(+) by 31+/-5% (P<0.01). While the vasodilatative effect of 20 mM K(+) was unaffected by L-NNA, NOS-inhibition resulted in vasoconstriction at > or = 40 mM K(+) (P<0.01). In presence of L-NNA, the basal vessel diameter was restored by either the NO-donor S-nitroso-N-acetylpenicillamine (SNAP) or the cell-permeable guanosine-3',5'-cyclic monophosphate (cGMP) analogue 8-Br-cGMP. Co-application of L-NNA with either SNAP or 8-Br-cGMP resulted in partial restitution of the vasodilatative effect of 40 mM K(+), respectively. In presence of the soluble guanylyl cyclase inhibitor 1 H-[l,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), the vascular response to 40 mM K(+) was abolished. Our findings together with findings from the literature indicate a modulator role of NO at K(+) > or = 40 mM K(+), involving a cGMP-dependent mechanism.

摘要

我们在离体大鼠大脑中动脉(MCA)的体外模型中研究了一氧化氮(NO)在血管对高腔外钾离子浓度反应中的作用。在对照条件下,大鼠MCA在20、30、40和60 mM钾离子浓度时扩张。在80 mM钾离子浓度时,出现轻微血管收缩。非特异性一氧化氮合酶(NOS)抑制剂L(ω)-硝基-L-精氨酸(L-NNA)使3 mM钾离子浓度时的静息张力增加31±5%(P<0.01)。虽然20 mM钾离子的舒张作用不受L-NNA影响,但NOS抑制在钾离子浓度≥40 mM时导致血管收缩(P<0.01)。在L-NNA存在的情况下,一氧化氮供体S-亚硝基-N-乙酰青霉胺(SNAP)或细胞可渗透的鸟苷-3',5'-环磷酸(cGMP)类似物8-溴-cGMP均可恢复基础血管直径。L-NNA与SNAP或8-溴-cGMP共同应用分别导致40 mM钾离子舒张作用部分恢复。在可溶性鸟苷酸环化酶抑制剂1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ)存在的情况下,对40 mM钾离子的血管反应被消除。我们的研究结果以及文献中的研究结果表明,在钾离子浓度≥40 mM时,NO具有调节作用,涉及cGMP依赖性机制。

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