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Interferon-gamma-inducible kynurenines/pteridines inflammation cascade: implications for aging and aging-associated psychiatric and medical disorders

机译:干扰素-γ诱导的犬尿氨酸/蝶啶类炎症级联反应:对衰老及与衰老相关的精神病和医学疾病的影响

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This review of literature and our data suggests that up-regulated production of interferon-gamma (IFNG) in periphery and brain triggers a merger of tryptophan (TRY)–kynurenine (KYN) and guanine–tetrahydrobiopterin (BH4) metabolic pathways into inflammation cascade involved in aging and aging-associated medical and psychiatric disorders (AAMPD) (metabolic syndrome, depression, vascular cognitive impairment). IFNG-inducible KYN/pteridines inflammation cascade is characterized by up-regulation of nitric oxide synthase (NOS) activity (induced by KYN) and decreased formation of NOS cofactor, BH4, that results in uncoupling of NOS that shifting arginine from NO to superoxide anion production. Superoxide anion and free radicals among KYN derivatives trigger phospholipase A2-arachidonic acid cascade associated with AAMPD. IFNG-induced up-regulation of indoleamine 2,3-dioxygenase (IDO), rate-limiting enzyme of TRY–KYN pathway, decreases TRY conversion into serotonin (substrate of antidepressant effect) and increases production of KYN associated with diabetes [xanthurenic acid (XA)], anxiety (KYN), psychoses and cognitive impairment (kynurenic acid). IFNG-inducible KYN/pteridines inflammation cascade is impacted by IFNG (+874) T/A genotypes, encoding cytokine production. In addition to literature data on KYN/TRY ratio (IDO activity index), we observe neopterin levels (index of activity of rate-limiting enzyme of guanine–BH4 pathway) to be higher in carriers of high (T) than of low (A) producers alleles; and to correlate with AAMPD markers (e.g., insulin resistance, body mass index, mortality risk), and with IFN-alpha-induced depression in hepatitis C patients. IFNG-inducible cascade is influenced by environmental factors (e.g., vitamin B6 deficiency increases XA formation) and by pharmacological agents; and might offer new approaches for anti-aging and anti-AAMPD interventions.
机译:这篇文献和我们的数据综述表明,外周和大脑中干扰素-γ(IFNG)的上调产生触发了色氨酸(TRY)-犬尿氨酸(KYN)和鸟嘌呤-四氢生物蝶呤(BH4)代谢途径合并进入炎症级联反应衰老和与衰老相关的医学和精神疾病(AAMPD)(代谢综合征,抑郁症,血管性认知障碍)。 IFNG诱导的KYN /蝶啶炎症级联的特征是一氧化氮合酶(NOS)活性上调(由KYN诱导)和NOS辅因子BH4形成减少,从而导致NOS解偶联,使精氨酸从NO转变为超氧阴离子。生产。 KYN衍生物中的超氧阴离子和自由基触发与AAMPD相关的磷脂酶A2-花生四烯酸级联反应。 IFNG诱导的吲哚胺2,3-二加氧酶(IDO)上调,TRY-KYN途径的限速酶,减少TRY转化为血清素(抗抑郁作用的底物),并增加与糖尿病相关的KYN的产生[黄嘌呤酸( XA)],焦虑(KYN),精神病和认知障碍(尿尿酸)。 IFNG诱导的KYN /蝶啶炎症级联受到编码细胞因子产生的IFNG(+874)T / A基因型的影响。除了有关KYN / TRY比(IDO活性指数)的文献数据外,我们还观察到高(T)携带者的新蝶呤水平(鸟嘌呤-BH4途径的限速酶活性指数)要高于低(A)携带者)生产者等位基因;并与丙型肝炎患者的AAMPD标记(例如,胰岛素抵抗,体重指数,死亡风险)以及IFN-α引起的抑郁症相关。 IFNG诱导级联反应受环境因素(例如,维生素B6缺乏症增加XA形成)和药理作用的影响;并可能提供抗衰老和抗AAMPD干预的新方法。

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