Robertson R Paul
Department of Medicine, University of Washington, 1959 N.E. Pacific Street, Seattle, Washington 98195, USA.
Discov Med. 2010 Feb;9(45):132-7.
Mainstays of therapy for type 2 diabetes involve drugs that are insulin-centric, i.e., they are designed to increase insulin secretion and decrease insulin resistance. The usual clinical course for people so treated is to have initially improved glycemic control but over time a need for intensification of drug-based treatment of hyperglycemia. The mechanism for this unrelenting deterioration of beta-cell function is related to chronic oxidative stress. This suggests that drug discovery should not exclusively focus on insulin-centric targets, but also include glucose-centric strategies, such as antioxidant protection of the beta-cell. This may facilitate repair of beta-cells undergoing damage by oxidative stress secondary to chronic hyperglycemia.
2型糖尿病的主要治疗方法涉及以胰岛素为核心的药物,即这些药物旨在增加胰岛素分泌并降低胰岛素抵抗。接受此类治疗的患者通常的临床病程是,最初血糖控制有所改善,但随着时间的推移,需要加强基于药物的高血糖治疗。β细胞功能这种持续恶化的机制与慢性氧化应激有关。这表明药物研发不应仅专注于以胰岛素为核心的靶点,还应包括以葡萄糖为核心的策略,例如对β细胞的抗氧化保护。这可能有助于修复因慢性高血糖继发氧化应激而受损的β细胞。