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瘦素选择性调节以高碳水化合物或高脂肪饮食喂养的尼罗罗非鱼的营养代谢。

Leptin Selectively Regulates Nutrients Metabolism in Nile Tilapia Fed on High Carbohydrate or High Fat Diet.

作者信息

Liu Cai-Zhi, He An-Yuan, Ning Li-Jun, Luo Yuan, Li Dong-Liang, Zhang Mei-Ling, Chen Li-Qiao, Du Zhen-Yu

机构信息

Laboratory of Aquaculture Nutrition and Environmental Health, School of Life Sciences, East China Normal University, Shanghai, China.

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine, Saint Louis, MO, United States.

出版信息

Front Endocrinol (Lausanne). 2018 Sep 27;9:574. doi: 10.3389/fendo.2018.00574. eCollection 2018.


DOI:10.3389/fendo.2018.00574
PMID:30405527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6201848/
Abstract

Leptin is known to inhibit appetite and promote energy metabolism in vertebrates. Leptin resistance (LR) commonly occurs in diet-induced obesity (DIO) in mammals. However, the roles of leptin in the energy homeostasis in DIO animals with LR remain unclear. Here we first verified the high expression of leptin in subcutaneous adipose tissue (SCAT) as in liver in Nile tilapia. Furthermore, we produced two types of DIO Nile tilapia by using a high-carbohydrate diet (HCD) or a high-fat diet (HFD), and confirmed the existence of LR in both models. Notably, we found that HCD-DIO fish retained leptin action in the activation of lipid metabolism and showed LR in glucose metabolism regulation, while this selective leptin action between lipid and glucose metabolism was reversed in HFD-DIO fish. Fasting the fish for 1 week completely recovered leptin actions in the regulation of lipid and glucose metabolism. Therefore, leptin may retain more of its activities in animals with LR than previously believed. Evolutionally, this selective regulation of leptin in nutrients metabolism could be an adaptive mechanism in animals to store surplus calories when different types of food are abundant.

摘要

已知瘦素可抑制脊椎动物的食欲并促进能量代谢。瘦素抵抗(LR)在哺乳动物的饮食诱导肥胖(DIO)中普遍存在。然而,瘦素在患有LR的DIO动物能量稳态中的作用仍不清楚。在此,我们首先证实尼罗罗非鱼皮下脂肪组织(SCAT)中的瘦素表达与肝脏中的一样高。此外,我们通过使用高碳水化合物饮食(HCD)或高脂肪饮食(HFD)产生了两种类型的DIO尼罗罗非鱼,并证实两种模型中均存在LR。值得注意的是,我们发现HCD-DIO鱼在脂质代谢激活中保留了瘦素作用,而在葡萄糖代谢调节中表现出LR,而这种在脂质和葡萄糖代谢之间的选择性瘦素作用在HFD-DIO鱼中则相反。将鱼禁食1周可完全恢复瘦素在脂质和葡萄糖代谢调节中的作用。因此,瘦素在患有LR的动物中可能保留了比以前认为更多的活性。从进化角度来看,瘦素在营养物质代谢中的这种选择性调节可能是动物在不同类型食物丰富时储存多余热量的一种适应性机制。

相似文献

[1]
Leptin Selectively Regulates Nutrients Metabolism in Nile Tilapia Fed on High Carbohydrate or High Fat Diet.

Front Endocrinol (Lausanne). 2018-9-27

[2]
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J Neuroendocrinol. 2015-4

[3]
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[4]
Systemic adaptation of lipid metabolism in response to low- and high-fat diet in Nile tilapia (Oreochromis niloticus).

Physiol Rep. 2015-8

[5]
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Eur Cytokine Netw. 2008-9

[6]
[The study on mechanism of appetite regulation in diet-induced obesity resistant rats].

Zhonghua Yu Fang Yi Xue Za Zhi. 2005-3

[7]
Altered hypothalamic leptin, insulin, and melanocortin binding associated with moderate-fat diet and predisposition to obesity.

Endocrinology. 2007-1

[8]
Identification of genetic loci associated with different responses to high-fat diet-induced obesity in C57BL/6N and C57BL/6J substrains.

Physiol Genomics. 2014-4-1

[9]
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[10]
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引用本文的文献

[1]
Adipocyte Hyperplasia Facilitated Adipose Tissue Expansion to Alleviate Hepatopancreas Injury in Nile Tilapia () Fed High-Fat Diet.

Aquac Nutr. 2025-7-2

[2]
Effects of ammonia exposure on the expression of IL-1β, CRH, and lep-a1 genes in common carp (Cyprinus carpio).

BMC Vet Res. 2025-5-28

[3]
Characterization of Leptin and Leptin Receptor Gene in the Siberian Sturgeon (): Molecular Cloning, Tissue Distribution, and Its Involvement in Feeding Regulation.

Int J Mol Sci. 2025-2-25

[4]
Betaine Supplementation Into High-Carbohydrate Diets Improves Feed Efficiency and Liver Health of by Increasing Taurine Synthesis.

Aquac Nutr. 2024-9-26

[5]
Study on the Function of Leptin Nutrient Acquisition and Energy Metabolism of Zebrafish ().

Int J Mol Sci. 2024-10-30

[6]
Dietary supplementation with succinic acid improves growth performance and flesh quality of adult Nile tilapia () fed a high-carbohydrate diet.

Anim Nutr. 2024-5-25

[7]
Dietary Bile Acid Supplementation Could Regulate the Glucose, Lipid Metabolism, and Microbiota of Common Carp ( L.) Fed with a High-Lipid Diet.

Aquac Nutr. 2023-5-24

[8]
High cholesterol intake remodels cholesterol turnover and energy homeostasis in Nile tilapia ().

Mar Life Sci Technol. 2023-2-16

[9]
Dietary betaine and/or TMAO affect hepatic lipid accumulation and glycometabolism of Megalobrama amblycephala exposed to a high-carbohydrate diet.

Fish Physiol Biochem. 2024-2

[10]
Inhibition of pyruvate dehydrogenase kinase improves carbohydrate utilization in Nile tilapia by regulating PDK2/4-PDHE1α axis and insulin sensitivity.

Anim Nutr. 2022-6-24

本文引用的文献

[1]
Diet-Induced Growth Is Regulated via Acquired Leptin Resistance and Engages a Pomc-Somatostatin-Growth Hormone Circuit.

Cell Rep. 2018-5-8

[2]
Insulin resistance in cavefish as an adaptation to a nutrient-limited environment.

Nature. 2018-3-21

[3]
Physiological and metabolic differences between visceral and subcutaneous adipose tissues in Nile tilapia .

Am J Physiol Regul Integr Comp Physiol. 2017-11-1

[4]
The destiny of the resistance/susceptibility against GCRV is controlled by epigenetic mechanisms in CIK cells.

Sci Rep. 2017-7-3

[5]
Assessing the Functional Role of Leptin in Energy Homeostasis and the Stress Response in Vertebrates.

Front Endocrinol (Lausanne). 2017-4-7

[6]
The cellular and molecular bases of leptin and ghrelin resistance in obesity.

Nat Rev Endocrinol. 2017-6

[7]
Mechanisms and metabolic regulation of PPARα activation in Nile tilapia (Oreochromis niloticus).

Biochim Biophys Acta. 2016-9

[8]
Goldfish Leptin-AI and Leptin-AII: Function and Central Mechanism in Feeding Control.

Int J Mol Sci. 2016-5-30

[9]
Leptin signaling regulates glucose homeostasis, but not adipostasis, in the zebrafish.

Proc Natl Acad Sci U S A. 2016-3-15

[10]
Identification of the Long-Sought Leptin in Chicken and Duck: Expression Pattern of the Highly GC-Rich Avian leptin Fits an Autocrine/Paracrine Rather Than Endocrine Function.

Endocrinology. 2016-2

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