Research Foundation ITSUU Laboratory, Tokyo, Japan.
Biol Pharm Bull. 2012;35(8):1206-12. doi: 10.1248/bpb.b12-00314.
Tamibarotene (Am80), a synthetic retinoid approved in Japan for treatment of acute promyelocytic leukemia (APL), is a retinoic acid receptor (RAR) agonist with high specificity for RARα and RARβ over RARγ. Temporarily and spatially specific expression of RARs suggests their pivotal roles in the adult brain. Am80 is considered to be a promising candidate drug for treatment of Alzheimer's disease (AD) because of its transcriptional controls of multiple target genes involved in etiology and pathology of AD. In APP23 AD model mice, administration of Am80 decreased the deposition of insoluble amyloid-β(42). In senescence-accelerated mice (SAMP8), Am80 ameliorated the decrease of cortical acetylcholine, as well as reducing anxiety in behavioral tests and improving the sleep deficit. Am80 also effected a significant improvement of memory in the rat scopolamine-induced memory deficit model. Like other retinoids, Am80 also has an immunomodulatory effect and reduces secretion of proinflammatory cytokines and chemokines by astrocytes and microglia surrounding amyloid-β plaques. In a rat experimental autoimmune encephalomyelitis model, Am80 reduced inflammatory cytokines and showed significant efficacy. Retinoids also promote differentiation of neural stem cells, and Am80 improved the recovery of spinal cord-injured rats. Am80 may also improve vascular factors involved in onset and/or progression of AD. Am80 has been in clinical use for treatment of APL in Japan since 2005, and has been reported to have fewer side effects than other retinoids. We have recently started a clinical study to evaluate the efficacy and safety of Am80 for the treatment of Alzheimer's disease.
他扎罗汀(Am80)是一种合成维 A 酸类药物,在日本被批准用于治疗急性早幼粒细胞白血病(APL),是一种对 RARα 和 RARβ 具有高特异性的维 A 酸受体(RAR)激动剂,而对 RARγ 的特异性较低。RARs 的暂时和空间特异性表达表明它们在成年大脑中具有关键作用。由于其对涉及 AD 病因和病理学的多个靶基因的转录调控作用,Am80 被认为是治疗 AD 的有前途的候选药物。在 APP23 AD 模型小鼠中,Am80 给药可减少不溶性淀粉样蛋白-β(42)的沉积。在衰老加速小鼠(SAMP8)中,Am80 改善了皮质乙酰胆碱的减少,以及减轻行为测试中的焦虑,并改善睡眠不足。Am80 还显著改善了东莨菪碱诱导的记忆缺陷大鼠模型的记忆。与其他维 A 酸类药物一样,Am80 也具有免疫调节作用,可减少淀粉样蛋白-β斑块周围星形胶质细胞和小胶质细胞分泌的促炎细胞因子和趋化因子。在大鼠实验性自身免疫性脑脊髓炎模型中,Am80 减少了炎症细胞因子,表现出显著疗效。维 A 酸类药物还可促进神经干细胞分化,Am80 改善了脊髓损伤大鼠的恢复。Am80 还可能改善 AD 发病和/或进展中涉及的血管因素。自 2005 年以来,Am80 一直在日本用于治疗 APL,据报道其副作用比其他维 A 酸类药物少。我们最近开始了一项评估 Am80 治疗 AD 的疗效和安全性的临床研究。