» Articles » PMID: 9037488

Actions of S-nitrosocysteine in the Nucleus Tractus Solitarii Are Unrelated to Release of Nitric Oxide

Overview
Journal Brain Res
Specialty Neurology
Date 1997 Jan 23
PMID 9037488
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Cardiovascular effects elicited by microinjection of L-S-nitrosocysteine in the nucleus tractus solitarii (NTS) were compared and contrasted with those produced by the dextroisomer, other nitric oxide donors and nitric oxide itself. L-S-nitrosocysteine produced dose-related decreases of arterial pressure and heart rate. In contrast, D-S-nitrosocysteine, S-nitrosoglutathione, glyceryl trinitrate, and sodium nitroprusside produced minimal responses that were not dose-related. Likewise, injection of cystine and nitric oxide, two products of S-nitrosocysteine breakdown, produced no significant response. Headspace analysis using chemiluminescence revealed that L- and D-S-nitrosocysteine released identical amounts of nitric oxide when exposed to homogenates of whole rat brain. Responses to L-S-nitrosocysteine were not affected by local injection of oxyhemoglobin or the nitric oxide synthase inhibitor L-nitroarginine methylester. Although injection of L-cysteine into the NTS produced responses similar to those seen with injection of L-S-nitrosocysteine, blockade of excitatory amino acid receptors with kynurenic acid inhibited responses to cysteine but not those to the nitrosothiol. The study demonstrates that S-nitrosocysteine is biologically active in the NTS. Its action is independent of release of nitric oxide from the nitrosothiol but may be mediated through stereoselective sites on target neurons.

Citing Articles

The epigenetic signatures of opioid addiction and physical dependence are prevented by D-cysteine ethyl ester and betaine.

McDonough J, Singhal N, Getsy P, Knies K, Knauss Z, Mueller D Front Pharmacol. 2024; 15:1416701.

PMID: 39281282 PMC: 11392886. DOI: 10.3389/fphar.2024.1416701.


Lipophilic analogues of D-cysteine prevent and reverse physical dependence to fentanyl in male rats.

Bates J, Getsy P, Coffee G, Baby S, MacFarlane P, Hsieh Y Front Pharmacol. 2024; 14:1336440.

PMID: 38645835 PMC: 11026688. DOI: 10.3389/fphar.2023.1336440.


L-cysteine ethylester reverses the adverse effects of morphine on breathing and arterial blood-gas chemistry while minimally affecting antinociception in unanesthetized rats.

Baby S, May W, Young A, Wilson C, Getsy P, Coffee G Biomed Pharmacother. 2024; 171:116081.

PMID: 38219385 PMC: 10922989. DOI: 10.1016/j.biopha.2023.116081.


L-cysteine ethyl ester prevents and reverses acquired physical dependence on morphine in male Sprague Dawley rats.

Bates J, Getsy P, Coffee G, Baby S, MacFarlane P, Hsieh Y Front Pharmacol. 2023; 14:1303207.

PMID: 38111383 PMC: 10726967. DOI: 10.3389/fphar.2023.1303207.


Hypoxia releases S-nitrosocysteine from carotid body glomus cells-relevance to expression of the hypoxic ventilatory response.

Seckler J, Getsy P, May W, Gaston B, Baby S, Lewis T Front Pharmacol. 2023; 14:1250154.

PMID: 37886129 PMC: 10598756. DOI: 10.3389/fphar.2023.1250154.