Correlation Between Catecholamine Release and Sodium Pump Inhibition in the Perfused Adrenal Gland of the Cat
Overview
Affiliations
1 Ca(2+) reintroduction to retrogradely perfused and ouabain (10(-4) M)-treated cat adrenal glands caused a catecholamine secretory response which was greater the longer the time of exposure to the cardiac glycoside. Such a response was proportional to the external Na(+) concentration [Na(+)](o).2 A qualitatively similar, yet smaller response was observed when glands were perfused with Krebs solution lacking K(+) ions; thus, K(+) deprivation mimicked the secretory effects of ouabain. Catecholamine secretion evoked by Ca(2+) reintroduction in K(+)-free solution (0-K(+)) was also proportional to [Na(+)](o) and greater the longer the time of exposure of the gland to 0-K(+) solution.3 The ionophore X537A also mimicked the ouabain effects, since Ca(2+) reintroduction to glands treated with this agent (25 muM) caused a sharp secretory response. When added together with X537A, ouabain (10(-4) M) did not modify the response to the ionophore.4 N-ethylmaleimide (NEM), another Na(+), K(+)-ATPase inhibitor, did not evoke the release of catecholamines; on the contrary, NEM (10(-4) M) inhibited the catecholamine secretory response to high [K(+)](o), acetylcholine, Ca(2+) reintroduction and ouabain.5 Ouabain (10(-4) M) inhibited the uptake of (86)Rb into adreno-medullary tissue by 60%. Maximal inhibition had already occurred 2 min after adding the drug, indicating a lack of temporal correlation between ATPase inhibition and the ouabain secretory response, which took longer (about 30-40 min) to reach its peak. NEM (10(-4) M) blocked (86)Rb uptake in a similar manner.6 The results are further evidence in favour of the presence of a Na(+)-Ca(2+) exchange system in the chromaffin cell membrane, probably involved in the control of [Ca(2+)](i) and in the modulation of catecholamine secretion. This system is activated by increasing [Na(+)](i), either directly (ionophore X537A, increased [Na(+)](o)) or indirectly (Na(+) pump inhibition). However, the simple inhibition of Na(+) pumping does not always lead to a catecholamine secretory response; such is the case for NEM.
Pintado A, Herrero C, Garcia A, Montiel C Br J Pharmacol. 2000; 130(8):1893-902.
PMID: 10952680 PMC: 1572275. DOI: 10.1038/sj.bjp.0703519.
Potentiation of K+-evoked catecholamine release in the cat adrenal gland treated with ouabain.
Garcia A, Garcia-Lopez E, Horga J, KIRPEKAR S, Montiel C, Sanchez-Garcia P Br J Pharmacol. 1981; 74(3):673-80.
PMID: 7296168 PMC: 2071758. DOI: 10.1111/j.1476-5381.1981.tb10478.x.
Wada A, Izumi F, Yanagihara N, Kobayashi H Naunyn Schmiedebergs Arch Pharmacol. 1985; 328(3):273-8.
PMID: 3982511 DOI: 10.1007/BF00515553.
Kitayama S, Morita K, Dohi T, Tsujimoto A Naunyn Schmiedebergs Arch Pharmacol. 1986; 332(1):66-9.
PMID: 3951566 DOI: 10.1007/BF00633199.
Nakazato Y, OHGA A, Yamada Y J Physiol. 1986; 374:475-91.
PMID: 3746701 PMC: 1182733. DOI: 10.1113/jphysiol.1986.sp016092.