Session: SAT 1-25-Glucocorticoid Actions & HPA Axis
Poster Board SAT-10
In order to identify GC regulated miRNAs blood was extracted from 10 healthy volunteers under four treatment conditions. Volunteers were fasted for 12h and infused with either saline or hydrocortisone (0.2mg/kg/h) this was followed by 4h of insulin infusion (100mU/m2.min). Samples were taken after fasting (+/- hydrocortisone) and after insulin infusion (+/- hydrocortisone). RNA was extracted and used in miRNA array analysis, providing full coverage of mirBASE17, including 1750 known human miRNAs. Expression of the most regulated miRNAs was measured by real-time PCR in human liver, adipose and muscle samples.
In the fasting state, hydrocortisone treatment significantly altered serum levels of 7 miRNAs, including some with predicted metabolic targets. Compared to fasting saline, the combination of hydrocortisone and insulin regulated 16 miRNAs, interestingly increasing miR-195 (associated with hypertension) and miR-144 (inhibition of insulin receptor substrate 1 [IRS1]). Compared to insulin alone, hydrocortisone regulated 25 miRNAs, interestingly increasing miR-637 (involved in adipocyte differentiation) and miR-145 (inhibition of IRS1 and 2). The 10 most highly regulated miRNAs were all expressed in the three key metabolic target tissues (liver, adipose and muscle). This study has identified novel profiles of GC regulated miRNAs in human serum associated with insulin sensitivity, a number of which have predicted and demonstrated metabolic targets. These data will allow us to investigate the endocrine regulation of miRNAs and their role in metabolic homeostasis and highlights potential miRNA targets that may underpin the tissue-specific effects of GCs on insulin action.
Nothing to Disclose: LLG, CD, JMH, PMS, GGL, JWT
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