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(Hypertension. 1997;30:1376-1381.)
© 1997 American Heart Association, Inc.

Articles

Reduced Cardiac Contractile Responsiveness to Isoproterenol in Obese Rabbits

Joan F. Carroll; Alan E. Jones; Robert L. Hester; Glenn A. Reinhart; Kathy Cockrell; ; H. Leland Mizelle

From the Department of Physiology and Biophysics, University of Mississippi Medical Center (Jackson).

Abstract Although obesity is characterized by increased sympathetic nervous system activity, there is often a paradoxical reduction in cardiovascular end-organ response to sympathetic stimulation. Mechanisms involved in reduced sympathetic responsiveness in obesity have not been well characterized. Therefore, we determined cardiac contractile responsiveness to ß-stimulation in the obese rabbit model using both isolated heart (IH) and isolated papillary muscle (IPM) preparations. Female New Zealand White rabbits were fed control (IH: n=9; IPM: n=6) or 10% fat diets (IH: n=9; IPM: n=7) for 12 weeks. Contractile responsiveness in the IH was determined using a modified Langendorff preparation to evaluate the dose-response relationship between isoproterenol and 1) peak developed pressure/g of left ventricular wet weight and 2) maximal rate of pressure development (+dP/dt/P). Contractile responsiveness in the IPM was determined using right ventricular papillary muscles to evaluate the dose-response relationship between isoproterenol and (1) peak developed tension (T)/mm² cross-sectional area (CSA) and (2) maximal rate of tension development (dT/dt/CSA). In the IH, baseline and maximum developed pressure/g were reduced in obese rabbits by 37% and 31%, respectively (P.05). In the IPM, baseline and maximum T/CSA responses were reduced in obese rabbits by 59% and 33%, respectively (P.05). Potency of isoproterenol as reflected by the EC₅₀ did not differ between lean and obese animals in either preparation. These results demonstrate that left ventricular contractility in obesity is reduced at baseline and in response to stimulation with isoproterenol and suggest that decreased responsiveness to ß-stimulation may be a factor in the obesity-related systolic dysfunction.

Key Words: heart • obesity • isoproterenol • rabbits • dysfunction, systolic

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