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Hydrogen sulfide as an endogenous regulator of vascular smooth muscle tone in trout
Abstract
Hydrogen sulfide (H 2 S) is an endogenous vasodilator in mammals, but its presence and function in other vertebrates is unknown. We generated H 2 S from NaHS and examined the effects on isolated efferent branchial arteries from steelhead (stEBA) or rainbow (rtEBA) trout. H 2 S concentration was measured colorimetrically (CM) and with ion-selective electrodes (ISE) in rainbow trout plasma. NaHS produced a triphasic response consisting of a relaxation (phase 1), constriction (phase 2), and relaxation (phase 3) in both unstimulated vessels and in stEBA precontracted with carbachol (Carb). Phase 1 and phase 3 in stEBA were decreased and phase 2 increased in unstimulated vessels by K+ATP channel inhibition (glibenclamide), or a cocktail of inhibitors of cyclooxygenase, lipoxygenase, and cytochrome P-450 (indomethacin, esculetin, and clotrimazole). Inhibition of soluble guanylate cyclase with ODQ or NS-2028 inhibited phase 3 in stEBA, although NaHS decreased cGMP production by rtEBA. stEBA phase 2 contractions were partially inhibited by the myosin light chain kinase inhibitor, ML-9, but unaffected by L-type calcium channel inhibition (methoxyverapamil), whereas contraction in rtEBA was partially inhibited by nifedipine or removal of extracellular calcium. Phase 3 relaxations were more pronounced in stEBA precontracted with Carb and norepinephrine (NE) than those contracted by KCl or K 2 SO 4. stEBA phase 2 and phase 3 responses were dose dependent (EC 50 = 1.1 ± 1.2 × 10-3 M and 6.7 ± 0.9 × 10-5 M, respectively; n = 7). NaHS was also vasoactive in steelhead bulbus arteriosus, celiacomesenteric arteries, and anterior cardinal veins. Rainbow trout plasma sulfide concentration was 4.0 ± 0.3 × 10-5 M, n = 4 (CM) and 3.8 ± 0.4 × 10-5 M, n = 9 (ISE); similar to phase 3 EC 50. Because NaHS has substantial vasoactive effects at physiological plasma concentrations, we propose that its soluble derivative, H 2 S, is a tonically active endogenous vasoregulator in trout.
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Cites
Dorman, D. C. (2002) · Toxicological Sciences · doi:10.1093/toxsci/65.1.18 · Cited by 362
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Ali, M. Y., Ping, C. Y., Mok, Y., Ling, L., Whiteman, M., Bhatia, M., & Moore, P. K. (2006) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706906 · Cited by 349
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Whiteman, M., Le Trionnaire, S., Chopra, M., Fox, B., & Whatmore, J. (2011) · Clinical Science · doi:10.1042/cs20110267 · Cited by 310
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Metadata
- Authors
- Dombkowski, R. A., Russell, M. J., & Olson, K. R.
- Venue
- American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
- Publisher
- American Physiological Society
- Published
- 2004-04
- Volume
- 286
- Issue
- 4
- Pages
- R678-R685
- ISSN
- 0363-6119 (ISSN-L)
- 1522-1490
- OpenAlex
- W2071309984
- Cited by
- 200
- References
- 1
- FWCI
- 3.00
- Type
- journal article
- Language
- en
- Open access
- closed
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- Dombkowski, R. A., Russell, M. J., & Olson, K. R. (2004). Hydrogen sulfide as an endogenous regulator of vascular smooth muscle tone in trout. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. https://doi.org/10.1152/ajpregu.00419.2003
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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