喂食高热量食物的突尼斯狒狒的行为:生化紊乱和组织病理学改变。

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Souhaieb Chrigui, Sihem Mbarek, Sameh Hadj Taieb, Zohra Haouas, Monssef Feki, Maha Benlarbi, Ayachi Zemmel, Fatiha Chigr, Nourhène Boudhrioua, Rafika Ben Chaouacha-Chekir
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引用次数: 0

摘要

这项研究调查了在三个月内喂食不同高热量饮食(HCD)的肥胖松鼠动物模型的生化紊乱和组织学改变。研究使用了四种饮食:低热量天然饮食(Chenopodiaceae Halophyte 植物作为对照)(LCD)、富含蛋白质的高标准碳水化合物饮食(HCD 0)、富含两种浓度脂肪的高碳水化合物饮食(HCD 1 和 HCD 2)。实验一个月后,所有接受高碳水化合物饮食的动物都出现了血脂异常,不同亚组的动物会出现或不出现肥胖和糖尿病。HCDs 导致血液中胆固醇、低密度脂蛋白胆固醇和甘油三酯水平显著升高,这表明它能快速诱导血脂异常,同时转氨酶活性显著升高,显示出明显的肝毒性。患糖尿病的动物表现出严重的肝损伤、脂肪组织变性和视网膜厚度明显降低。肥胖猪似乎是研究营养代谢疾病的极佳动物模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Behaviour of Tunisian Psammomys obesus fed high-calorie diets: biochemical disturbance and histopathological alterations.

This work investigated the biochemical disturbances and histological alteration in Psammomys obesus animal model fed different high calorie diets (HCDs) during three months. Four diets were used: a low-calorie natural diet, Chenopodiaceae halophyte plant used as control (LCD), a high standard carbohydrate diet rich in protein, HCD 0, a high carbohydrate diet rich in two concentrations of fat, HCD 1 and HCD 2. All animals having received HCDs developed dyslipidemia after one month of experiment with distinction of different sub-groups developing or not obesity and diabetes. HCDs induced a remarkable increasing in blood cholesterol, LDL-cholesterol and triglyceride levels indicating a fast induction of dyslipidemia and a significant increase of aminotransaminases activities revealing a pronounced hepatotoxicity. Animal developing diabetes showed a severe hepatic injury, a degeneration of the adipose tissue and a significant reduction of retinal thickness. P. obesus seems to be an excellent animal model to investigate nutritional metabolic diseases.

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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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