Santhanam Anantha Vijay R, d'Uscio Livius V, He Tongrong, Das Pritam, Younkin Steven G, Katusic Zvonimir S
Departments of Anesthesiology, and Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
Department of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA.
J Neurochem. 2015 Sep;134(6):1129-38. doi: 10.1111/jnc.13205. Epub 2015 Jul 15.
In this study, we tested the hypothesis that reduced bioavailability of tetrahydrobiopterin (BH4) is a major mechanism responsible for pathogenesis of endothelial dysfunction in cerebral microvessels of transgenic mice expressing the Swedish double mutation of human amyloid precursor protein (APP) (Tg2576 mice). Endothelial nitric oxide synthase (eNOS) protein expression was significantly increased in cerebral vasculature of Tg2576 mice. In contrast, bioavailability of BH4 was significantly reduced (p < 0.05). Moreover, superoxide anion production was increased in cerebral microvessels of Tg2576 mice (p < 0.05). Incubation with NOS inhibitor, Nω-nitro-L-arginine methyl ester, decreased superoxide anion indicating that uncoupled eNOS is most likely the source of superoxide anion. Increasing BH4 bioavailability either exogenously by BH4 supplementation or endogenously by treatment with the selective peroxisome proliferator-activated receptor--delta activator GW501516 (2 mg/kg/day, 14 days) attenuated eNOS uncoupling and decreased superoxide anion production in cerebral microvessels of Tg2576 mice (p < 0.05). Treatment with GW501516 restored the biological activity of endothelial nitric oxide in cerebral microvessels of Tg2576 mice, as indicated by the increased nitrite/nitrate content and 3,5-cyclic guanosine monophosphate levels (p < 0.05). Our studies indicate that sub-optimal BH4 bioavailability in cerebral vasculature is an important contributor to oxidant stress and endothelial dysfunction in Tg2576 mouse model of Alzheimer's disease. Existing evidence suggests that Aβ peptides-induced up-regulation of expression and activity of NADPH oxidase causes increased production of superoxide anion (.O2(-)). .O2(-) can also be converted to hydrogen peroxide (H2O2) by enzymatic activity of superoxide dismutase (SOD) or spontaneous dismutation. Elevation of .O2(-) and H2O2 might cause oxidation of tetrahydrobiopterin (BH4) to dihydrobiopterin (BH2) and subsequent uncoupling of endothelial nitric oxide synthase (eNOS) (a) thus reducing levels of nitric oxide (NO) and 3',5'-cyclic guanosine monophosphate (cGMP). Supplementation of BH4 or activation of PPARδ prevents detrimental effects of eNOS uncoupling by restoring bioavailability of BH4 and scavenging of .O2(-), respectively (b). Activation of PPARδ also increases expression of catalase thereby inactivating H2O2. Generation of H2O2 by uncoupled eNOS in cerebral microvessels of Tg2576 mice is hypothetical.
在本研究中,我们验证了以下假说:四氢生物蝶呤(BH4)生物利用度降低是导致表达人淀粉样前体蛋白(APP)瑞典双突变的转基因小鼠(Tg2576小鼠)脑微血管内皮功能障碍发病的主要机制。Tg2576小鼠脑血管中内皮型一氧化氮合酶(eNOS)蛋白表达显著增加。相比之下,BH4的生物利用度显著降低(p<0.05)。此外,Tg2576小鼠脑微血管中超氧阴离子生成增加(p<0.05)。用一氧化氮合酶抑制剂Nω-硝基-L-精氨酸甲酯孵育可降低超氧阴离子,这表明解偶联的eNOS很可能是超氧阴离子的来源。通过补充BH4外源性增加或用选择性过氧化物酶体增殖物激活受体δ激动剂GW501516(2mg/kg/天,14天)处理内源性增加BH4的生物利用度,可减轻Tg2576小鼠脑微血管中的eNOS解偶联并降低超氧阴离子生成(p<0.05)。如亚硝酸盐/硝酸盐含量和3,5-环鸟苷单磷酸水平升高所示(p<0.05),用GW501516处理可恢复Tg2576小鼠脑微血管中内皮一氧化氮的生物活性。我们的研究表明,脑微血管中BH4生物利用度欠佳是阿尔茨海默病Tg2576小鼠模型中氧化应激和内皮功能障碍的重要促成因素。现有证据表明,Aβ肽诱导的NADPH氧化酶表达和活性上调导致超氧阴离子(·O2-)生成增加。·O2-也可通过超氧化物歧化酶(SOD)的酶活性或自发歧化转化为过氧化氢(H2O2)。·O2-和H2O2升高可能导致四氢生物蝶呤(BH4)氧化为二氢生物蝶呤(BH2),随后内皮型一氧化氮合酶(eNOS)解偶联(a),从而降低一氧化氮(NO)和3',5'-环鸟苷单磷酸(cGMP)水平。补充BH4或激活PPARδ分别通过恢复BH4的生物利用度和清除·O2-来预防eNOS解偶联的有害影响(b)。激活PPARδ还可增加过氧化氢酶的表达,从而使H2O2失活。Tg2576小鼠脑微血管中解偶联的eNOS产生H2O2是一种假说。