Search for dissertations about: "Adipose Tissue physiology"
Showing result 1 - 5 of 45 swedish dissertations containing the words Adipose Tissue physiology.
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1. Role of caveolin-1 in brown adipose tissue
Abstract : Caveolae are 50-100 nm invaginations in the plasma membrane. Caveolae and the protein caveolin-1 (Cav1) have been shown to be important in many signaling pathways in different cell types; however, in some cell types caveolae and Cav1 do not seem to affect the investigated signaling pathways. READ MORE
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2. Energy flow and metabolic efficiency attributed to brown adipose tissue
Abstract : The large capacity of brown adipose tissue (BAT) to expend energy as heat makes it an interesting potential player in weight regulation and other metabolic conditions. This is of particular interest as it has been recognized that adult humans possess BAT. READ MORE
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3. Who is Who in the Adipose Organ : A look at the Heterogeneity of Adipocyte Biology
Abstract : The increasing prevalence of obesity and related health complications, such as type 2 diabetes, cardiovascular disease and cancer, demands thorough investigation of the underlying processes. One of the key tissues investigated in this context is adipose tissue. READ MORE
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4. β-Adrenergic Signalling Through mTOR
Abstract : Adrenergic signalling is part of the sympathetic nervous system and is activated upon stimulation by the catecholamines epinephrine and norepinephrine. This regulates heart rate, energy mobilization, digestion and helps to divert blood flow to important organs. READ MORE
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5. Myosin 1c taking adrenergic metabolism for a spin : More than a motor protein
Abstract : Metabolic diseases like type II diabetes (T2D) and obesity largely stems from an unbalanced energy homeostasis with the fails of the insulin pathway to the point in which the glucose homeostasis is severely disturbed leading to hyperglycemia. We have investigated if the β-adrenergic signaling pathways, in both brown adipose tissue (BAT) and skeletal muscle, could be used as a strategy to alleviate metabolic disease. READ MORE