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. Author manuscript; available in PMC: 2015 May 14.
Published in final edited form as: Cardiovasc Drugs Ther. 2015 Apr;29(2):121–127. doi: 10.1007/s10557-015-6580-y

Fig. 5.

Fig. 5

Peripheral administration of irisin reduced blood pressure. Blood pressure and cardiac contractility were measured in control (SD) or spontaneously hypertensive (SHR) rats. IgG Fc peptide and r-irisin were delivered via femoral vein injection. (a) Control IgG Fc peptide did not change blood pressure; r-irisin (2–4 μg) significantly reduced blood pressure (upper panel). Neither IgG Fc nor r-irisin changed cardiac contractility (lower panel). (b) r-irisin(2–8 μg) significantly reduced blood pressure in SHR. (c) Vasoactivity of mesenteric artery rings with or without endothelium was measured. The rings were pre-constricted with 10−6 M phenylephrine (PE). When the contraction of rings reached plateau level, relaxation in response to r-irisin was assayed in the presence or absence of 10 μM glibenclamide (a KATP channel blocker)