Psychiatry and Inflammation Program, Department of Psychiatry, Tufts University/Tufts Medical Center, Boston, MA, USA.
J Neural Transm (Vienna). 2011 Jan;118(1):75-85. doi: 10.1007/s00702-010-0475-7. Epub 2010 Sep 2.
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.
这篇文献综述和我们的数据表明,外周和大脑中干扰素-γ(IFNG)的过度产生触发了色氨酸(TRY)-犬尿氨酸(KYN)和鸟嘌呤-四氢生物蝶呤(BH4)代谢途径与衰老和衰老相关的医学和精神障碍(AAMPD)(代谢综合征、抑郁症、血管性认知障碍)炎症级联反应的融合。IFNG 诱导的 KYN/蝶呤炎症级联反应的特征是一氧化氮合酶(NOS)活性的上调(由 KYN 诱导)和 NOS 辅助因子 BH4 的形成减少,导致 NOS 解偶联,将精氨酸从 NO 转移到超氧化物阴离子的产生。KYN 衍生物中的超氧化物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-双加氧酶(IDO)的上调,TRY-KYN 途径的限速酶,减少 TRY 转化为 5-羟色胺(抗抑郁作用的底物),增加 KYN 的产生与糖尿病[黄尿酸(XA)]、焦虑(KYN)、精神病和认知障碍(喹啉酸)有关。IFNG 诱导的 KYN/蝶呤炎症级联反应受到 IFNG(+874)T/A 基因型的影响,该基因型编码细胞因子的产生。除了关于 KYN/TRY 比值(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 途径限速酶的活性指数)高于低(A)产生物等位基因;并与 AAMPD 标志物(如胰岛素抵抗、体重指数、死亡率风险)相关,以及与丙型肝炎患者 IFN-α 诱导的抑郁相关。IFNG 诱导的级联反应受环境因素(如维生素 B6 缺乏增加 XA 形成)和药物的影响;并可能为抗衰老和抗 AAMPD 干预提供新方法。