A peroxisome proliferator-activated receptor gamma agonist influenced daily profile of energy expenditure in genetically obese diabetic rats.

Y. Yoshida, M. Ichikawa, M. Ohta, S. Kanai, M. Kobayash, Y. Ichimaru, T. Shimazoe, Shigenori Watanabe, A. Funakoshi, Kyoko Miyasak
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引用次数: 10

Abstract

Otsuka Long Evans Tokushima Fatty (OLETF) rats were developed as a model of non-insulin-dependent diabetes mellitus (NIDDM) with mild obesity. We reported that the daily profiles of energy expenditure associated with two peaks (one between 05:00 and 08:00 and the other between 20:00 and 22:00) were observed at 8 weeks of age (without NIDDM), while these two peaks disappeared at 24 weeks of age with NIDDM. As a new anti-diabetic drug, a peroxisome proliferator-activated receptor y agonist pioglitazone hydrochloride has been developed, we examined whether pioglitazone normalized daily profiles of energy expenditure at 24 weeks of age. A control diet and pioglitazone (0.1%)-containing diet were fed from 6 weeks of age. The two peaks of daily profiles of energy expenditure, which disappeared in OLETF rats with the control diet at 24 weeks of age, were reproduced by administration of pioglitazone. The respiratory quotient was lower and fat derived energy used for combustion was increased by pioglitazone at both ages. The body weight, daily food intake, plasma levels of fat, insulin, leptin and the wet weight of visceral fat were not influenced, but the levels of blood hemoglobin Alc and plasma tumor necrosis factor a were decreased by pioglitazone. Administration of pioglitazone improved daily profiles of energy expenditure via affecting glucose and fat metabolisms.
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过氧化物酶体增殖物激活受体γ激动剂影响遗传性肥胖糖尿病大鼠的每日能量消耗。
大冢Long Evans德岛脂肪(OLETF)大鼠作为非胰岛素依赖型糖尿病(NIDDM)伴轻度肥胖模型。我们报道了在8周龄(非NIDDM)时观察到与两个峰值相关的每日能量消耗谱(一个在05:00至08:00之间,另一个在20:00至22:00之间),而这两个峰值在24周龄(NIDDM)时消失。作为一种新的抗糖尿病药物,过氧化物酶体增殖物激活受体激动剂盐酸吡格列酮已经被开发出来,我们研究了吡格列酮是否使24周龄的每日能量消耗曲线正常化。6周龄饲喂对照饲粮和吡格列酮(0.1%)饲粮。24周龄时,正常饮食的OLETF大鼠每日能量消耗曲线的两个峰值消失,吡格列酮可以重现。吡格列酮降低了呼吸商,增加了用于燃烧的脂肪来源能量。吡格列酮对体重、日摄食量、血浆脂肪水平、胰岛素、瘦素和内脏脂肪湿重均无影响,但对血血红蛋白Alc和血浆肿瘤坏死因子a水平有降低作用。吡格列酮通过影响葡萄糖和脂肪代谢改善每日能量消耗概况。
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