β3-Adrenergically induced glucose uptake in brown adipose tissue is independent of UCP1 presence or activity: Mediation through the mTOR pathway
暂无分享,去创建一个
S. Stone-Elander | T. Bengtsson | J. Nedergaard | Anna L. Sandström | Robert I. Csikasz | Li Lu | Nodi Dehvari | J. Olsen | Anette I. Öberg
[1] T. Yen. Antiobesity and antidiabetic beta-agonists: lessons learned and questions to be answered. , 1994, Obesity research.
[2] C. Chresta,et al. Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR) , 2009, The Biochemical journal.
[3] A. Barlier,et al. 18F-FDG Avidity of Pheochromocytomas and Paragangliomas: A New Molecular Imaging Signature? , 2009, Journal of Nuclear Medicine.
[4] S. Lindahl,et al. Halothane Selectively Inhibits Nonshivering Thermogenesis: Possible Implications for Thermoregulation during Anesthesia of Infants , 1995, Anesthesiology.
[5] B. Cannon,et al. Thermogenic Responses in Brown Fat Cells Are Fully UCP1-dependent , 2000, The Journal of Biological Chemistry.
[6] K. Flaherty,et al. Sarcolipin is a newly identified regulator of muscle-based thermogenesis in mammals , 2012, Nature Medicine.
[7] J. Granneman,et al. White adipose tissue contributes to UCP1-independent thermogenesis. , 2003, American journal of physiology. Endocrinology and metabolism.
[8] F. Lönnqvist,et al. Tissue distribution of beta 3-adrenergic receptor mRNA in man. , 1993, The Journal of clinical investigation.
[9] J. Himms-Hagen,et al. Thermogenesis in brown adipose tissue as an energy buffer. Implications for obesity. , 1984, The New England journal of medicine.
[10] G. Cooney,et al. The effect of insulin and noradrenaline on the uptake of 2‐[1‐14C]deoxyglucose in vivo by brown adipose tissue and other glucose‐utilising tissues of the mouse , 1985, FEBS letters.
[11] S. Lindahl,et al. Thermogenesis in Brown Adipocytes Is Inhibited by Volatile Anesthetic Agents A Factor Contributing to Hypothermia in Infants? , 1994, Anesthesiology.
[12] H. Lang,et al. Hyperfixation diffuse de la graisse brune à la tomoscintigraphie par émission de positons couplée à la tomodensitométrie (TEP-TDM) dans l’exploration d’un phéochromocytome extra surrénalien , 2005 .
[13] M. Miyagawa,et al. High Incidence of Metabolically Active Brown Adipose Tissue in Healthy Adult Humans , 2009, Diabetes.
[14] J. Chambard,et al. JCB_201403080 1..10 , 2014 .
[15] R. Lecomte,et al. In vivo measurement of energy substrate contribution to cold‐induced brown adipose tissue thermogenesis , 2015, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[16] S. Lindahl,et al. Inhibitory effects of halothane on the thermogenic pathway in brown adipocytes: localization to adenylyl cyclase and mitochondrial fatty acid oxidation. , 2004, Biochemical pharmacology.
[17] P. Brust,et al. Dissociation Between Brown Adipose Tissue 18F-FDG Uptake and Thermogenesis in Uncoupling Protein 1–Deficient Mice , 2017, The Journal of Nuclear Medicine.
[18] G. Bronnikov,et al. Norepinephrine Induces Vascular Endothelial Growth Factor Gene Expression in Brown Adipocytes through a β-Adrenoreceptor/cAMP/Protein Kinase A Pathway Involving Src but Independently of Erk1/2* , 2000, The Journal of Biological Chemistry.
[19] B. Cannon,et al. Only UCP1 can mediate adaptive nonshivering thermogenesis in the cold , 2001, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[20] M. Saito,et al. Uncoupling protein 1 is necessary for norepinephrine-induced glucose utilization in brown adipose tissue. , 2005, Diabetes.
[21] Jan Nedergaard,et al. The presence of UCP1 demonstrates that metabolically active adipose tissue in the neck of adult humans truly represents brown adipose tissue , 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[22] Jan Nedergaard,et al. Brown adipose tissue: function and physiological significance. , 2004, Physiological reviews.
[23] S. Keipert,et al. Brite/beige fat and UCP1 - is it thermogenesis? , 2014, Biochimica et biophysica acta.
[24] A. Doria,et al. Activation of human brown adipose tissue by a β3-adrenergic receptor agonist. , 2015, Cell metabolism.
[25] T. Bengtsson,et al. New powers of brown fat: fighting the metabolic syndrome. , 2011, Cell metabolism.
[26] T. Bengtsson,et al. β-Adrenoceptors, but not α-adrenoceptors, stimulate AMP-activated protein kinase in brown adipocytes independently of uncoupling protein-1 , 2005, Diabetologia.
[27] A. Marette,et al. Noradrenaline stimulates glucose transport in rat brown adipocytes by activating thermogenesis. Evidence that fatty acid activation of mitochondrial respiration enhances glucose transport. , 1991, The Biochemical journal.
[28] Hitoshi Yamashita,et al. Mice lacking mitochondrial uncoupling protein are cold-sensitive but not obese , 1997, nature.
[29] F. Assimacopoulos-Jeannet,et al. Stimulatory effect of cold adaptation on glucose utilization by brown adipose tissue. Relationship with changes in the glucose transporter system. , 1987, The Journal of biological chemistry.
[30] Manjot Kaur,et al. Continuous glucose monitoring in normal mice and mice with prediabetes and diabetes. , 2006, Diabetes technology & therapeutics.
[31] J. Nedergaard,et al. Cold‐induced expression of the VEGF gene in brown adipose tissue is independent of thermogenic oxygen consumption , 2005, FEBS letters.
[32] B. Cannon,et al. Beta 3- and alpha1-adrenergic Erk1/2 activation is Src- but not Gi-mediated in Brown adipocytes. , 2000, The Journal of biological chemistry.
[33] N. Sakane,et al. Anti-obesity effect of CL 316,243, a highly specific beta 3-adrenoceptor agonist, in mice with monosodium-L-glutamate-induced obesity. , 1994, European journal of endocrinology.
[34] L. Bukowiecki,et al. Stimulatory effects of cold exposure and cold acclimation on glucose uptake in rat peripheral tissues. , 1990, The American journal of physiology.
[35] P. Arner,et al. Cidea improves the metabolic profile through expansion of adipose tissue , 2015, Nature Communications.
[36] O. Morel,et al. Visualization of Activated BAT in Mice, with FDG-PET and Its Relation to UCP1 , 2013 .
[37] J. Orava,et al. Functional brown adipose tissue in healthy adults. , 2009, The New England journal of medicine.
[38] Naishi Li,et al. Activating Brown Adipose Tissue for Weight Loss and Lowering of Blood Glucose Levels: A MicroPET Study Using Obese and Diabetic Model Mice , 2014, PloS one.
[39] T. Bengtsson,et al. Beta-adrenoceptors, but not alpha-adrenoceptors, stimulate AMP-activated protein kinase in brown adipocytes independently of uncoupling protein-1. , 2005, Diabetologia.
[40] M. Cawthorne. Does brown adipose tissue have a role to play in glucose homeostasis? , 1989, Proceedings of the Nutrition Society.
[41] L. Bukowiecki,et al. Chronic norepinephrine infusion stimulates glucose uptake in white and brown adipose tissues. , 1994, The American journal of physiology.
[42] S. Lindahl,et al. Thermogenesis Inhibition in Brown Adipocytes Is a Specific Property of Volatile Anesthetics , 2003, Anesthesiology.
[43] T. Bengtsson,et al. Unexpected evidence for active brown adipose tissue in adult humans. , 2007, American journal of physiology. Endocrinology and metabolism.
[44] M. Hall,et al. mTORC2 sustains thermogenesis via Akt‐induced glucose uptake and glycolysis in brown adipose tissue , 2016, EMBO molecular medicine.
[45] B. Cannon,et al. β3- and α1-Adrenergic Erk1/2 Activation Is Src- but Not Gi-mediated in Brown Adipocytes* , 2000, The Journal of Biological Chemistry.
[46] Clark R. Andersen,et al. Brown Adipose Tissue Improves Whole-Body Glucose Homeostasis and Insulin Sensitivity in Humans , 2014, Diabetes.
[47] E. Palmer,et al. Identification and importance of brown adipose tissue in adult humans. , 2009, The New England journal of medicine.
[48] B. Cannon,et al. UCP1 is essential for adaptive adrenergic nonshivering thermogenesis. , 2006, American journal of physiology. Endocrinology and metabolism.
[49] J. Ukropec,et al. UCP1-independent Thermogenesis in White Adipose Tissue of Cold-acclimated Ucp1-/- Mice* , 2006, Journal of Biological Chemistry.
[50] B. Kingwell,et al. Ephedrine activates brown adipose tissue in lean but not obese humans , 2013, Diabetologia.
[51] W. D. van Marken Lichtenbelt,et al. Cold-activated brown adipose tissue in healthy men. , 2009, The New England journal of medicine.
[52] Zhen-ping Zhu,et al. Supplemental Data Hypoxia-Independent Angiogenesis in Adipose Tissues during Cold Acclimation , 2008 .
[53] Carolina E. Hagberg,et al. Adrenergically stimulated blood flow in brown adipose tissue is not dependent on thermogenesis. , 2015, American journal of physiology. Endocrinology and metabolism.
[54] E. Horton,et al. CL-316,243, a β3-Specific Adrenoceptor Agonist, Enhances Insulin-Stimulated Glucose Disposal in Nonobese Rats , 1997, Diabetes.
[55] R. Wahl,et al. Radionuclide imaging metabolic activity of brown adipose tissue in a patient with pheochromocytoma. , 2004, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.
[56] J. Himms-Hagen,et al. Effect of CL-316,243, a thermogenic beta 3-agonist, on energy balance and brown and white adipose tissues in rats. , 1994, The American journal of physiology.
[57] H. Lang,et al. [Diffuse uptake of brown fat on computed-tomography coupled positron emission tomoscintigraphy (PET-CT) for the exploration of extra-adrenal pheochromocytoma]. , 2006, Annales d'endocrinologie.
[58] M. Shafiee Ardestani,et al. Anti Diabetic effect of CL 316,243 (A β3-Adrenergic Agonist) by Down Regulation of Tumour Necrosis Factor (TNF-α) Expression , 2012, PloS one.