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Carolina Gustavsson, Tomoyoshi Soga, Erik Wahlström, Mattias Vesterlund, Alireza Azimi, Gunnar Norstedt, and Petra Tollet-Egnell

. 2005 ) and antioxidant ( Louet et al . 2004 , Baba et al . 2005 , Borrás et al . 2005 ) properties. Oestrogens have also been shown to inhibit lipogenesis and stimulate lipolysis in abdominal visceral fat depots, to promote use of lipid as a fuel

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Eva Tudurí, Monica Imbernon, Rene Javier Hernández-Bautista, Marta Tojo, Johan Fernø, Carlos Diéguez, and Rubén Nogueiras

-Hyiaman et al . 2008 ). In addition, activation of CB1 increases lipogenesis and inflammation and reduces lipolysis, in the white adipose tissue (WAT) ( Silvestri & Di Marzo 2013 ). Furthermore, CB1 activation impairs insulin sensitivity, as evidenced by

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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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Ana Luísa Neves, João Coelho, Luciana Couto, Adelino Leite-Moreira, and Roberto Roncon-Albuquerque Jr

of triglyceride, hepatic de novo fatty acid synthesis, and lipolysis. High doses of LPS produce hypertriglyceridemia by decreasing lipoprotein catabolism. Administration of TNF antibodies or IL1 receptor antagonist did not prevent the increase in

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Subhamoy Dasgupta and Bert W O'Malley

protected from high-fat diet-induced obesity and exhibit increased insulin sensitivity, higher lipolysis, and reduced fat uptake ( Picard et al . 2002 ). Loss of Src-2 −/− also affects the hepatic glucose release due to decreased expression of glucose-6

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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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Kazuyoshi Ukena, Tomohiro Osugi, Jérôme Leprince, Hubert Vaudry, and Kazuyoshi Tsutsui

-induced lipolysis ( Malumba et al . 2010 ). As 3T3-L1 cells express the QRFPR-encoding gene, it appears that 26RFa/QRFP may act in an autocrine/paracrine manner to regulate adipogenesis ( Malumba et al . 2010 ). According to Alonzeau et al . (2013) , 26RFa

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Sofia A Rahman, Azizun Nessa, and Khalid Hussain

inappropriate release leads to persistent hyperinsulinaemic hypoglycaemia (HH). This drives glucose into the insulin sensitive tissues and simultaneously suppresses lipolysis and ketogenesis. The combined hypoketonaemic and hypoglycaemic characteristic of CHI

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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