Sarker M H, Fraser P A
Centre for Cardiovascular Biology and Medicine, King's College London, New Hunt's House, Guy's Campus, London SE1 1UL, UK.
J Physiol. 2002 Apr 1;540(Pt 1):209-18. doi: 10.1113/jphysiol.2001.012912.
Inflammatory mediators have a role in the formation of cerebral oedema and there is evidence that cGMP is an important signal in vascular permeability increase. We have investigated the role and the source of cGMP in mediating the permeability response to acutely applied bradykinin and the histamine H(2) agonist dimaprit on single cerebral venular capillaries, by using the single vessel occlusion technique. We found that 8-bromo-cGMP applied acutely resulted in a small and reversible permeability increase with a log EC(50) -7.2 +/- 0.15 M. KT 5823, the inhibitor of cGMP-dependent protein kinase, abolished the permeability responses to both bradykinin and dimaprit, while zaprinast, an inhibitor of type 5 phosphodiesterase, potentiated the response to bradykinin. On the other hand, L-NMMA blocked the response to dimaprit, but not that to bradykinin. Inhibitors of soluble guanylyl cyclase, LY 85353 and methylene blue, also inhibited the permeability response to dimaprit, but not bradykinin. The permeability responses to the natriuretic peptides ANP and CNP were of similar magnitude to that of bradykinin with log EC(50) -10.0 +/- 0.33 M and -8.7 +/- 0.23 M, respectively. The natriuretic peptide receptor antagonist HS-142-1 blocked permeability responses to bradykinin as well as to ANP, and leukotriene D(4) blocked the responses to CNP and bradykinin, but not to dimaprit. In conclusion, the histamine H(2) receptor appears to signal via cGMP that is generated by a NO and soluble guanylyl cyclase, while bradykinin B(2) receptor also signals via cGMP but through particulate guanylyl cyclase.
炎症介质在脑水肿形成中起作用,并且有证据表明环磷酸鸟苷(cGMP)是血管通透性增加的重要信号。我们通过使用单血管闭塞技术,研究了cGMP在介导对急性应用的缓激肽和组胺H₂激动剂二甲双胍的通透性反应中的作用及来源,该反应发生在单个脑静脉毛细血管上。我们发现,急性应用8-溴-cGMP会导致通透性出现小幅度的可逆性增加,其对数半数有效浓度(log EC₅₀)为-7.2±0.15 M。cGMP依赖性蛋白激酶抑制剂KT 5823消除了对缓激肽和二甲双胍的通透性反应,而5型磷酸二酯酶抑制剂扎普司特增强了对缓激肽的反应。另一方面,L-硝基精氨酸甲酯(L-NMMA)阻断了对二甲双胍的反应,但未阻断对缓激肽的反应。可溶性鸟苷酸环化酶抑制剂LY 85353和亚甲蓝也抑制了对二甲双胍的通透性反应,但未抑制对缓激肽的反应。对利钠肽心房钠尿肽(ANP)和C型利钠肽(CNP)的通透性反应幅度与缓激肽相似,其对数半数有效浓度分别为-10.0±0.33 M和-8.7±0.23 M。利钠肽受体拮抗剂HS-142-1阻断了对缓激肽以及ANP的通透性反应,白三烯D₄阻断了对CNP和缓激肽的反应,但未阻断对二甲双胍的反应。总之,组胺H₂受体似乎通过由一氧化氮(NO)和可溶性鸟苷酸环化酶产生的cGMP来传递信号,而缓激肽B₂受体也通过cGMP传递信号,但通过颗粒性鸟苷酸环化酶。