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Pierre Poinsot, Martin Schwarzer, Noël Peretti, and François Leulier

actions or lipolysis ( Bergan-Roller & Sheridan 2017 ). Anabolic actions of GH in juvenile growth act by well-known mechanism associated with positive nitrogen balance, protein synthesis in muscle and stimulation of the longitudinal bone growth ( Chikani

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Johan Svensson, Sofia Movérare-Skrtic, Sara Windahl, Charlotte Swanson, and Klara Sjögren

some or all of the lipolysis that is independent of hormone-sensitive lipase ( Soni et al . 2004 ), was up-regulated in muscle by E 2 , indicating increased utilization of free fatty acids as fuel. Synaptic transmission DHT up-regulated several genes

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Qi Zhang, Qin Zhu, Ruyuan Deng, Feiye Zhou, Linlin Zhang, Shushu Wang, Kecheng Zhu, Xiao Wang, Libin Zhou, and Qing Su

reticulum-tethered transcription factor cAMP responsive element-binding protein, hepatocyte specific, regulates hepatic lipogenesis, fatty acid oxidation, and lipolysis upon metabolic stress in mice . Hepatology 55 1070 – 1082 . ( https://doi.org/10

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Davids Fridmanis, Ramona Petrovska, Dace Pjanova, Helgi B Schiöth, and Janis Klovins

, Kovalitskaia et al . 2008 ). In the adrenal cortex, MC2R affects glucocorticoid production ( Clark & Cammas 1996 ) and synthesis of its own mRNA ( Naville et al . 1999 ). Research with mouse adipocytes has shown that MC2R participates in lipolysis ( Boston

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Jin-Seung Choung, Young-Sun Lee, and Hee-Sook Jun

lipolysis and free fatty acid utilization, contributing to the activation of UCP-1. β 3 -adrenergic receptors are thought to play a role in thermogenesis in brown fat and skeletal muscle, induce adaptive non-shivering thermogenesis and stimulate UCP1

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Ting Qi, Yanming Chen, Honggui Li, Ya Pei, Shih-Lung Woo, Xin Guo, Jiajia Zhao, Xiaoxian Qian, Joseph Awika, Yuqing Huo, and Chaodong Wu

and resveratrol ameliorate muscle insulin resistance through preventing lipolysis and inflammation in hypoxic adipose tissue . Cell Signal 28 1401 – 1411 . ( doi:10.1016/j.cellsig.2016.06.018 ) Zheng J Woo S-L Hu X Botchlett R

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Rebecca Roy, Caitlyn Nguyen-Ngo, and Martha Lappas

force in term pregnant rat myometrium . Journal of Physiology 593 4603 – 4614 . ( https://doi.org/10.1113/JP270631 ) Heimann E Nyman M Degerman E 2015 Propionic acid and butyric acid inhibit lipolysis and de novo lipogenesis and increase

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Edwin J W Geven, Folkert Verkaar, Gert Flik, and Peter H M Klaren

, Schreck 2000 ). Cortisol stimulates gluconeogenesis and lipolysis ( Sheridan 1988 , van der Boon et al. 1991 ), which result in increased plasma glucose and free fatty acid levels. These catabolic actions of cortisol reflect its glucocorticoid potency

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L J Moran, P A Mundra, H J Teede, and P J Meikle

metabolic effects including suppression of lipogenesis and enhancement of lipolysis ( Shirouchi et al . 2007 ). Elevated lysophosphatidylcholine may indicate an increase in phospholipase activity which is highly expressed in the atherogenic plaque and

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Elisa Manieri and Guadalupe Sabio

secretion of adipokines ( Gavrilova et al . 2000 ). In the obese state, adipocyte enlargement induces molecular and cellular alterations that affect whole-body metabolic homeostasis. Increased lipolysis in adipocytes leads to increased hyperlipidaemia and