Dopamine selectively inhibits aldosterone responses to angiotensin II in man. 1984

R M Carey, and C R Drake

Previous studies have demonstrated that dopamine inhibits the aldosterone response to angiotensin II in the sodium deplete state in man, but not in the normal sodium balance state. In this study we investigated nine normal male volunteers in balance at 10 mEq sodium intake to determine whether the inhibitory effect of dopamine is selective for angiotensin II-induced aldosterone secretion or also inhibits ACTH-induced stimulation of aldosterone secretion. After 2 h dopamine infusion, angiotensin II was administered in cumulative doses of 0.5, 1, 2, 4 and 6 pmol/kg/min, each dose for 30 min. Aldosterone responses to angiotensin II were greater with vehicle than with dopamine at doses of 2, 4 and 6 pmol/kg/min (P less than 0.05). The slope of the angiotensin II-aldosterone dose-response curve was steeper with vehicle (0.46) than with dopamine (0.26) (P less than 0.05). However, when ACTH in doses of 0.5, 1, 2 and 5 U/h was substituted for angiotensin II, aldosterone responses were similar with vehicle and dopamine, as were the dose-response slopes. Thus, dopamine inhibits angiotensin II- but not ACTH-induced aldosterone secretion in sodium deficient man.

UI MeSH Term Description Entries
D008297 Male Males
D004298 Dopamine One of the catecholamine NEUROTRANSMITTERS in the brain. It is derived from TYROSINE and is the precursor to NOREPINEPHRINE and EPINEPHRINE. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (RECEPTORS, DOPAMINE) mediate its action. Hydroxytyramine,3,4-Dihydroxyphenethylamine,4-(2-Aminoethyl)-1,2-benzenediol,Dopamine Hydrochloride,Intropin,3,4 Dihydroxyphenethylamine,Hydrochloride, Dopamine
D004305 Dose-Response Relationship, Drug The relationship between the dose of an administered drug and the response of the organism to the drug. Dose Response Relationship, Drug,Dose-Response Relationships, Drug,Drug Dose-Response Relationship,Drug Dose-Response Relationships,Relationship, Drug Dose-Response,Relationships, Drug Dose-Response
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000324 Adrenocorticotropic Hormone An anterior pituitary hormone that stimulates the ADRENAL CORTEX and its production of CORTICOSTEROIDS. ACTH is a 39-amino acid polypeptide of which the N-terminal 24-amino acid segment is identical in all species and contains the adrenocorticotrophic activity. Upon further tissue-specific processing, ACTH can yield ALPHA-MSH and corticotrophin-like intermediate lobe peptide (CLIP). ACTH,Adrenocorticotropin,Corticotropin,1-39 ACTH,ACTH (1-39),Adrenocorticotrophic Hormone,Corticotrophin,Corticotrophin (1-39),Corticotropin (1-39),Hormone, Adrenocorticotrophic,Hormone, Adrenocorticotropic
D000450 Aldosterone A hormone secreted by the ADRENAL CORTEX that regulates electrolyte and water balance by increasing the renal retention of sodium and the excretion of potassium. Aldosterone, (+-)-Isomer,Aldosterone, (11 beta,17 alpha)-Isomer
D000451 Mineralocorticoid Receptor Antagonists Drugs that bind to and block the activation of MINERALOCORTICOID RECEPTORS by MINERALOCORTICOIDS such as ALDOSTERONE. Aldosterone Antagonist,Aldosterone Antagonists,Aldosterone Receptor Antagonist,Mineralocorticoid Antagonist,Mineralocorticoid Receptor Antagonist,Aldosterone Receptor Antagonists,Mineralocorticoid Antagonists,Antagonist, Aldosterone,Antagonist, Aldosterone Receptor,Antagonist, Mineralocorticoid,Antagonist, Mineralocorticoid Receptor,Antagonists, Aldosterone,Antagonists, Aldosterone Receptor,Antagonists, Mineralocorticoid,Antagonists, Mineralocorticoid Receptor,Receptor Antagonist, Aldosterone,Receptor Antagonist, Mineralocorticoid,Receptor Antagonists, Aldosterone,Receptor Antagonists, Mineralocorticoid
D000804 Angiotensin II An octapeptide that is a potent but labile vasoconstrictor. It is produced from angiotensin I after the removal of two amino acids at the C-terminal by ANGIOTENSIN CONVERTING ENZYME. The amino acid in position 5 varies in different species. To block VASOCONSTRICTION and HYPERTENSION effect of angiotensin II, patients are often treated with ACE INHIBITORS or with ANGIOTENSIN II TYPE 1 RECEPTOR BLOCKERS. Angiotensin II, Ile(5)-,Angiotensin II, Val(5)-,5-L-Isoleucine Angiotensin II,ANG-(1-8)Octapeptide,Angiotensin II, Isoleucine(5)-,Angiotensin II, Valine(5)-,Angiotensin-(1-8) Octapeptide,Isoleucine(5)-Angiotensin,Isoleucyl(5)-Angiotensin II,Valyl(5)-Angiotensin II,5 L Isoleucine Angiotensin II,Angiotensin II, 5-L-Isoleucine
D012964 Sodium A member of the alkali group of metals. It has the atomic symbol Na, atomic number 11, and atomic weight 23. Sodium Ion Level,Sodium-23,Ion Level, Sodium,Level, Sodium Ion,Sodium 23
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor

Related Publications

R M Carey, and C R Drake
September 1988, The Journal of pharmacology and experimental therapeutics,
R M Carey, and C R Drake
January 2000, Journal of hypertension,
R M Carey, and C R Drake
May 1986, Clinical science (London, England : 1979),
R M Carey, and C R Drake
December 1993, Journal of hypertension. Supplement : official journal of the International Society of Hypertension,
R M Carey, and C R Drake
December 1992, Acta psychiatrica Scandinavica,
R M Carey, and C R Drake
July 1987, The Journal of clinical endocrinology and metabolism,
R M Carey, and C R Drake
July 1979, The Journal of clinical investigation,
R M Carey, and C R Drake
August 1989, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme,
R M Carey, and C R Drake
December 1989, Journal of hypertension. Supplement : official journal of the International Society of Hypertension,
Copied contents to your clipboard!