Abstract Adropin is the secreted peptide that enhances glucose homeostasis and hepatic steatosis when administered to induced diet obese mice. It is not clear that the Adropin is the peptide hormone administered by metabolic state' signals. The serum adropin is being regulated by diet and metabolic status. The role of the adropin deficiency in the metabolic homeostasis is investigated by adropin knockout mice using C57BL/6j background. Adropin is considered to be the peptide hormone administered by feeding and fasting. Adropin levels in fed conditions increase with the dietary fat contents and dietary macronutrients. Adropin is not needed to regulate food intake but its functions affect adiposity. It is involvedinpreventingdyslipidemia,impairedglucosetoleranceandinsulin resistance. Introduction Adropin is considered to be a peptide harmone which plays a significant role in regulating glucose and lipid homeostasis. Adropin levels can be seen in mice consumed a low carbohydrate high fat diet and lower levels can be seen in mice consumed a high carbohydrate low fat diet. Thus, adropin levels are considered to be dietary macronutrients which increase with the dietary fat contents. Serum adropin levels in chow fed conditions are high and suppressed by diet induced obesityandfasting.Adropindeficiencyoccursduetoconsumptionofhigh carbohydrate or obesity that results in increase in the risk of Metabolic Syndrome. Adropin functions affect adiposity and lipid metabolism which imposes significant impact on the body. Adropin mechanism depicts that it impose negative effect on the glucose homeostasis and associated with increasing fat mass. 1
The main aim for the treatment of the type 2 diabetes is to maintain glycemic control (Kumar et al., 2012). The limited effectiveness of current treatment techniques and increase in the fatty liver disease and type 2 diabetes has encouraged the investigation on metabolic homeostasis for improving treatment efficacy. The first objective is to examine whether serum adropin is being regulated by obesity, nutrition and fasting. The second objective is to examine the phenotype of the adropin deficient mice and identify adropin deficiency is enough for affecting metabolic homeostasis with the use of adropin knockout mice. 2
References Kumar, K., Zhang, J., Gao, S., Rossi, J., McGuinness, O., Halem, H., Culler, M., Mynatt, R. and Butler, A. (2012).Adropin Deficiency Is Associated With Increased Adiposity and Insulin Resistance.[online]www.ncbi.nlm.nih.gov.Availableat: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905465/ [Accessed 28 Feb. 2019]. 3