Kaneto Hideaki, Nakatani Yoshihisa, Miyatsuka Takeshi, Kawamori Dan, Matsuoka Taka-aki, Matsuhisa Munehide, Kajimoto Yoshitaka, Ichijo Hidenori, Yamasaki Yoshimitsu, Hori Masatsugu
Department of Internal Medicine and Therapeutics, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.
Nat Med. 2004 Oct;10(10):1128-32. doi: 10.1038/nm1111. Epub 2004 Sep 26.
The JNK pathway is known to be activated in several tissues in the diabetic state, and is possibly involved in the development of insulin resistance and suppression of insulin biosynthesis. Here we show a potential new therapy for diabetes using cell-permeable JNK-inhibitory peptide. Intraperitoneal administration of the peptide led to its transduction into various tissues in vivo, and this treatment markedly improved insulin resistance and ameliorated glucose tolerance in diabetic mice. These data indicate that the JNK pathway is critically involved in diabetes and that the cell-permeable JNK-inhibitory peptide may have promise as a new therapeutic agent for diabetes.
已知JNK通路在糖尿病状态下的多种组织中被激活,并且可能参与胰岛素抵抗的发展以及胰岛素生物合成的抑制。在此,我们展示了一种使用细胞渗透性JNK抑制肽治疗糖尿病的潜在新方法。腹腔注射该肽可使其在体内转导至各种组织,并且这种治疗显著改善了糖尿病小鼠的胰岛素抵抗并改善了葡萄糖耐量。这些数据表明JNK通路在糖尿病中起关键作用,并且细胞渗透性JNK抑制肽有望成为一种新的糖尿病治疗药物。