Faraci Frank M, Lynch Cynthia, Lamping Kathryn G
Dept. of Internal Medicine, E318-2 GH, Univ. of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
Am J Physiol Heart Circ Physiol. 2004 Dec;287(6):H2871-6. doi: 10.1152/ajpheart.00392.2004.
ADP mediates platelet-induced relaxation of blood vessels and may function as an important intercellular signaling molecule in the brain. We used pharmacological and genetic approaches to examine mechanisms that mediate responses of cerebral arterioles to ADP, including the role of endothelial nitric oxide synthase (eNOS). We examined responses of cerebral arterioles (control diameter approximately 30 microm) in anesthetized wild-type (WT, eNOS+/+) and eNOS-deficient (eNOS-/-) mice using a cranial window. In WT mice, local application of ADP produced vasodilation that was not altered by indomethacin but was reduced by approximately 50% by NG-nitro-L-arginine (L-NNA) or 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) (inhibitors of NOS and soluble guanylate cyclase, respectively). In eNOS-/- mice, responses to ADP were largely preserved, and a significant component of the response was resistant to L-NNA (a finding similar to that in WT mice treated with L-NNA). In the absence of L-NNA, responses to ADP were markedly reduced by charybdotoxin plus apamin [inhibitors of Ca2+-dependent K+ channels and responses mediated by endothelium-derived hyperpolarizing factor (EDHF)] in both WT and eNOS-/- mice. Thus pharmacological and genetic evidence suggests that a significant portion of the response to ADP in cerebral microvessels is mediated by a mechanism independent of eNOS. The eNOS-independent mechanism is functional in the absence of inhibited eNOS and most likely is mediated by an EDHF.
二磷酸腺苷(ADP)介导血小板诱导的血管舒张,可能作为大脑中一种重要的细胞间信号分子发挥作用。我们采用药理学和遗传学方法,研究介导脑微动脉对ADP反应的机制,包括内皮型一氧化氮合酶(eNOS)的作用。我们使用颅窗,检测了麻醉的野生型(WT,eNOS+/+)和eNOS基因敲除(eNOS-/-)小鼠脑微动脉(对照直径约30微米)的反应。在野生型小鼠中,局部应用ADP可引起血管舒张,吲哚美辛对此无影响,但NG-硝基-L-精氨酸(L-NNA)或1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ)(分别为一氧化氮合酶和可溶性鸟苷酸环化酶的抑制剂)可使其降低约50%。在eNOS-/-小鼠中,对ADP的反应基本保留,且反应的一个重要部分对L-NNA具有抗性(这一发现与用L-NNA处理的野生型小鼠相似)。在无L-NNA的情况下,野生型和eNOS-/-小鼠对ADP的反应均被卡律蝎毒素加蜂毒明肽[Ca2+依赖性钾通道抑制剂以及内皮源性超极化因子(EDHF)介导的反应抑制剂]显著降低。因此,药理学和遗传学证据表明,脑微血管对ADP反应的很大一部分是由一种独立于eNOS的机制介导的。在eNOS未受抑制的情况下,这种独立于eNOS的机制发挥作用,很可能是由EDHF介导的。