Advertisement
Journal Home
Search for

Volume 118, Issue 9, Pages 998-1003 (September 2005)


View previous. 13 of 37 View next.

Hemodynamic effects of ephedra-free weight-loss supplements in humans

Christine A. Haller, MDCorresponding Author Informationemail address, Neal L. Benowitz, MD, Peyton Jacob III, PhD

Abstract 

Purpose

Ephedra-free weight loss dietary supplements containing bitter orange (Citrus aurantium), a botanical source of the adrenergic amines synephrine and octopamine, have quickly emerged on consumer markets to replace banned ephedra products. These supplements may have some of the health risks associated with ephedra, but studies in humans are lacking. Our aim was to characterize the pharmacokinetics and cardiovascular effects of C. aurantium dietary supplements.

Subjects and methods

Ten healthy adult nonsmokers participated in a randomized, double-blind, placebo-controlled, three-arm crossover study. Single doses of C. aurantium (Advantra Z) containing 46.9 mg synephrine, Xenadrine EFX, a multi-component formulation containing 5.5 mg synephrine, and placebo were administered with a one-week washout.

Results

Compared with placebo, Xenadrine EFX but not Advantra Z increased systolic and diastolic blood pressure with peak changes from baseline at 2 hours of 9.6 ± 6.2 mm Hg systolic (P = 0.047), and 9.1 ± 7.8 mm Hg diastolic (P = 0.002). Heart rate was increased from baseline at 6 hours compared with placebo (16.7 beats per minute with Xenadrine EFX, P = 0.011; 11.4 beats per minute with Advantra Z, P = 0.031). Dose-adjusted synephrine pharmacokinetics were similar between treatments with tmax = 90 min, t1/2 = 3.0 hours, V/F = 16347 L, and CL/F = 88.9 L/min for Xenadrine EFX.

Conclusion

Ephedra-free weight loss supplements have significant cardiovascular stimulant actions, similar to ephedra. These effects are not likely caused by C. aurantium alone, because an eightfold higher dose of synephrine (Advantra Z) had no effect on blood pressure, but may be attributable to caffeine and other stimulants in the multi-component formulation

Division of Clinical Pharmacology and Experimental Therapeutics, Department of Medicine, University of California, San Francisco.

Corresponding Author InformationRequests for reprints should be addressed to Christine A. Haller, MD, University of California, San Francisco, Box 1220, San Francisco, CA 94143.

 Drs. Haller and Benowitz have served as paid expert witnesses in litigation involving manufacturers of dietary supplements.

PII: S0002-9343(05)00200-7

doi:10.1016/j.amjmed.2005.02.034


View previous. 13 of 37 View next.

Advertisement