SUMMARY Endogenous opiate peptides can regulate neuroendocrine and circulatory responses to behavioral stress and may be important in the pathogenic effects of sympathoadrenal reactivity. We tested this hypothesis by examining the effect of the opiate antagonist naloxone on blood pressure responses to behavioral stress in young adults with high, medium, or low casual blood pressures. Naloxone increased mean arterial pressure responses to stress in subjects with low casual pressure, but had no significant effect on responses in subjects with high casual pressure. These results suggest opioidergic inhibition of sympathetic nervous system responses may be deficient in persons at risk for essential hypertension. The mechanism underlying sympathoadrenal hyperreactivity is unknown despite the potential importance of this issue to the etiology of essential hypertension. Opiate peptide systems have a close anatomical relationship to circulatory reflex pathways, and their role in blood pressure regulation has only recently been appreciated. For example, opioid cell bodies or receptors have been found in nucleus tractus solitarius, locus coeruleus, nucleus intermediolateralis, and other nuclei involved in central control of blood pressure. Additionally, these peptides are present in anterior and