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作为进食抑制剂的内源性糖酸衍生物。

Endogenous sugar acid derivative acting as a feeding suppressant.

作者信息

Plata-Salamán C R, Oomura Y, Shimizu N

出版信息

Physiol Behav. 1986;38(3):359-73. doi: 10.1016/0031-9384(86)90107-1.

Abstract

Evidence suggests that endogenous sugar acids 3,4-dihydroxybutanoic acid (2-deoxytetronic acid, 2-DTA) and 2,4,5-trihydroxypentanoic acid (3-deoxypentonic acid, 3-DPA) may participate in the regulation of feeding. To study the effect of 2-buten-4-olide, a 2-DTA synthetic derivative, on food intake, male Wistar rats were subjected to various applications. Intraperitoneal administration of 2-buten-4-olide in doses of 30 to 100 mg/kg, decreased food intake dose-dependently by reducing meal frequency, meal size and eating rate, and prolonging meal duration, latency to eat the first meal after injection and post-prandial intermeal intervals. Drinking patterns and locomotor activity were not significantly affected. Administration of 2-buten-4-olide intragastrically in doses of 50 to 300 mg/kg, and intra-third cerebroventricularly in doses of 1.2 to 5.0 mumol/rat, dose-dependently reduced food intake. This and previous evidence suggest that: 2-DTA and its derivatives that share its bioactive components suppress food intake in the rat; They might represent a new category of potential therapeutic agents for hyperphagia and obesity.

摘要

有证据表明内源性糖酸3,4-二羟基丁酸(2-脱氧四羟酸,2-DTA)和2,4,5-三羟基戊酸(3-脱氧戊糖酸,3-DPA)可能参与进食调节。为研究2-DTA合成衍生物2-丁烯-4-内酯对食物摄入的影响,对雄性Wistar大鼠进行了各种应用实验。腹腔注射剂量为30至100mg/kg的2-丁烯-4-内酯,通过降低进餐频率、进餐量和进食速率,并延长进餐持续时间、注射后首次进餐的延迟时间和餐后餐间间隔,剂量依赖性地减少食物摄入。饮水模式和运动活动未受到显著影响。胃内给予剂量为50至300mg/kg的2-丁烯-4-内酯,以及脑室内注射剂量为1.2至5.0μmol/大鼠的2-丁烯-4-内酯,均剂量依赖性地减少食物摄入。这一结果以及之前的证据表明:2-DTA及其具有相同生物活性成分的衍生物可抑制大鼠的食物摄入;它们可能代表一类用于治疗食欲亢进和肥胖症的新型潜在治疗药物。

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