Miki Satomi, Suzuki Jun-Ichiro, Kunimura Kayo, Morihara Naoaki
Central Research Institute, Wakunaga Pharmaceutical Co., Ltd., Akitakata-shi, Hiroshima 739-1195, Japan.
Research and Development, Wakunaga of America Co., Ltd., Mission Viejo, CA 92691, USA.
Exp Ther Med. 2020 Feb;19(2):1462-1467. doi: 10.3892/etm.2019.8372. Epub 2019 Dec 27.
AMP-activated protein kinase (AMPK) is an ubiquitously expressed serine/threonine kinase and an important regulator of energy metabolism. The decreased activity of AMPK induced by low-grade chronic inflammation has been implicated in several diseases, including type 2 diabetes and atherosclerosis. However, the activation of AMPK by natural and synthetic products can ameliorate these diseases through the inhibition of inflammation. For example, aged garlic extract (AGE) has been shown to enhance the phosphorylation of Thr172 of the α-subunit of AMPK in several tissues of disease model animals. In addition, AGE has been reported to suppress the progression of atherosclerotic plaque formation in an animal model of atherosclerosis. Moreover, AGE has been found to decrease the level of plasma glycated albumin and to improve hyperglycemia in an animal model of type 2 diabetes. These inhibitory effects of AGE are induced by the suppression of the inflammatory response. In the present review, we discuss the mechanisms through which AGE activates AMPK, as well as the mechanisms through which the activation of AMPK by AGE modulates the inflammatory response in disease models.
AMP激活的蛋白激酶(AMPK)是一种广泛表达的丝氨酸/苏氨酸激酶,也是能量代谢的重要调节因子。低度慢性炎症诱导的AMPK活性降低与包括2型糖尿病和动脉粥样硬化在内的多种疾病有关。然而,天然和合成产物对AMPK的激活可通过抑制炎症来改善这些疾病。例如,在疾病模型动物的多个组织中,老化大蒜提取物(AGE)已被证明可增强AMPKα亚基Thr172位点的磷酸化。此外,据报道,AGE在动脉粥样硬化动物模型中可抑制动脉粥样硬化斑块形成的进展。而且,在2型糖尿病动物模型中,AGE已被发现可降低血浆糖化白蛋白水平并改善高血糖。AGE的这些抑制作用是通过抑制炎症反应诱导的。在本综述中,我们讨论了AGE激活AMPK的机制,以及AGE激活AMPK调节疾病模型中炎症反应的机制。