夜间间歇性暴露于绿光和白光下可激活雄性Wistar大鼠肝糖原分解和糖异生活动。

Q3 Pharmacology, Toxicology and Pharmaceutics
Abayomi O Ige, Olubori S Adekanye, Elsie O Adewoye
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Thereafter, retro-orbital sinus blood was obtained after light thiopental anaesthesia and serum insulin was determined. Liver samples were also obtained and evaluated for glycogen, PGC-1α, and G6Pase activity. Insulin resistance was estimated using the HOMA-IR equation. Results Body weight and blood glucose on days 7 and 14 increased in groups II and III compared to control. Hepatic PGC-1α and G6Pase increased in group II (2.33 ± 0.31; 2.07 ± 0.22) and III (2.31 ± 0.20; 0.98 ± 0.23) compared to control (1.73 ± 0.21; 0.47 ± 0.11). Hepatic glycogen was 71.8 and 82.4% reduced in groups II and III compared to control. Insulin in group II increased (63.6%) whiles group III values reduced (27.3%) compared to control. Insulin resistance increased in group II (0.29 ± 0.09) compared to control (0.12 ± 0.03) and group III (0.11 ± 0.03), respectively. 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引用次数: 2

摘要

目的:有报道称夜间光照(LAN)会损害血糖调节。肝脏调节血糖的机制受几个因素的影响,包括过氧化物酶体增殖物激活受体γ辅助激活因子-1α (PGC-1α)和葡萄糖-6-磷酸酶(G6Pase)。本研究探讨了间歇性暴露于绿白lan对雄性Wistar大鼠肝糖调节因子的影响。方法:将动物分为三组。第一组(对照组)暴露在正常的住房条件下。II组和III组每天分别暴露于绿色或白色LAN 2小时(晚上7-9点),持续14天。于第0、7、14天监测体重和血糖。轻度硫喷妥钠麻醉后取眶后窦血,测定血清胰岛素。获得肝脏样本并评估糖原、PGC-1α和G6Pase活性。使用HOMA-IR方程估计胰岛素抵抗。结果:与对照组相比,II组和III组第7天和第14天体重和血糖升高。II组肝脏PGC-1α和G6Pase升高(2.33±0.31;(2.07±0.22)和(2.31±0.20);0.98±0.23),对照组(1.73±0.21;0.47±0.11)。与对照组相比,II组和III组肝糖原分别降低71.8和82.4%。与对照组相比,II组胰岛素升高(63.6%),而III组胰岛素降低(27.3%)。胰岛素抵抗组(0.29±0.09)高于对照组(0.12±0.03)和对照组(0.11±0.03)。结论:在早期暗期暴露于绿白lan 2小时可增加肝糖原分解和糖异生活动,导致血糖升高。在雄性Wistar大鼠中,暴露于绿色而非白色LAN可能易导致胰岛素抵抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermittent exposure to green and white light-at-night activates hepatic glycogenolytic and gluconeogenetic activities in male Wistar rats.
Abstract Objectives Exposure to light-at-night (LAN) has been reported to impair blood glucose regulation. The liver modulates blood glucose through mechanisms influenced by several factors that include peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1α) and glucose-6-phosphatase (G6Pase). This study investigated the effect of intermittent exposure to green and white LAN on some hepatic glucose regulatory factors in male Wistar rats. Methods Animals were divided into three equal groups. Group I (control) was exposed to normal housing conditions. Groups II and III were each daily exposed to either green or white LAN for 2 h (7–9 pm) for 14 days. Body weight and blood glucose was monitored on days 0, 7, and 14. Thereafter, retro-orbital sinus blood was obtained after light thiopental anaesthesia and serum insulin was determined. Liver samples were also obtained and evaluated for glycogen, PGC-1α, and G6Pase activity. Insulin resistance was estimated using the HOMA-IR equation. Results Body weight and blood glucose on days 7 and 14 increased in groups II and III compared to control. Hepatic PGC-1α and G6Pase increased in group II (2.33 ± 0.31; 2.07 ± 0.22) and III (2.31 ± 0.20; 0.98 ± 0.23) compared to control (1.73 ± 0.21; 0.47 ± 0.11). Hepatic glycogen was 71.8 and 82.4% reduced in groups II and III compared to control. Insulin in group II increased (63.6%) whiles group III values reduced (27.3%) compared to control. Insulin resistance increased in group II (0.29 ± 0.09) compared to control (0.12 ± 0.03) and group III (0.11 ± 0.03), respectively. Conclusions Exposure to 2 h green and white LAN in the early dark phase increases hepatic glycogenolysis and gluconeogenetic activities resulting in increased blood glucose. In male Wistar rats, exposure to green but not white LAN may predispose to insulin resistance.
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来源期刊
Journal of Basic and Clinical Physiology and Pharmacology
Journal of Basic and Clinical Physiology and Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
3.90
自引率
0.00%
发文量
53
期刊介绍: The Journal of Basic and Clinical Physiology and Pharmacology (JBCPP) is a peer-reviewed bi-monthly published journal in experimental medicine. JBCPP publishes novel research in the physiological and pharmacological sciences, including brain research; cardiovascular-pulmonary interactions; exercise; thermal control; haematology; immune response; inflammation; metabolism; oxidative stress; and phytotherapy. As the borders between physiology, pharmacology and biochemistry become increasingly blurred, we also welcome papers using cutting-edge techniques in cellular and/or molecular biology to link descriptive or behavioral studies with cellular and molecular mechanisms underlying the integrative processes. Topics: Behavior and Neuroprotection, Reproduction, Genotoxicity and Cytotoxicity, Vascular Conditions, Cardiovascular Function, Cardiovascular-Pulmonary Interactions, Oxidative Stress, Metabolism, Immune Response, Hematological Profile, Inflammation, Infection, Phytotherapy.
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