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Acrolein but not its metabolite, 3-Hydroxypropylmercapturic acid (3HPMA), activates vascular transient receptor potential Ankyrin-1 (TRPA1): Physiological to toxicological implications.
- Source :
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Toxicology and applied pharmacology [Toxicol Appl Pharmacol] 2021 Sep 01; Vol. 426, pp. 115647. Date of Electronic Publication: 2021 Jul 13. - Publication Year :
- 2021
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Abstract
- Acrolein, an electrophilic α,β-unsaturated aldehyde, is present in foods and beverages, and is a product of incomplete combustion, and thus, reaches high ppm levels in tobacco smoke and structural fires. Exposure to acrolein is linked with cardiopulmonary toxicity and cardiovascular disease risk. The hypothesis of this study is the direct effects of acrolein in isolated murine blood vessels (aorta and superior mesenteric artery, SMA) are transient receptor potential ankyrin-1 (TRPA1) dependent. Using isometric myography, isolated aorta and SMA were exposed to increasing levels of acrolein. Acrolein inhibited phenylephrine (PE)-induced contractions (approximately 90%) in aorta and SMA of male and female mice in a concentration-dependent (0.01-100 μM) manner. The major metabolite of acrolein, 3-hydroxypropylmercapturic acid (3HPMA), also relaxed PE-precontracted SMA. As the SMA was 20× more sensitive to acrolein than aorta (SMA EC <subscript>50</subscript> 0.8 ± 0.2 μM; aorta EC <subscript>50</subscript>  > 29.4 ± 4.4 μM), the mechanisms of acrolein-induced relaxation were studied in SMA. The potency of acrolein-induced relaxation was inhibited significantly by: 1) mechanically-impaired endothelium; 2) Nω-Nitro-L-arginine methyl ester hydrochloride (L-NAME); 3) guanylyl cyclase (GC) inhibitor (ODQ); and, 4) a TRPA1 antagonist (A967079). TRPA1 positive immunofluorescence was present in the endothelium. Compared with other known TRPA1 agonists, including allyl isothiocyanate (AITC), cinnamaldehyde, crotonaldehyde, and formaldehyde, acrolein stimulated a more potent TRPA1-dependent relaxation. Acrolein, at high concentration [100 μM], induced tension oscillations (spasms) independent of TRPA1 in precontracted SMA but not in aorta. In conclusion, acrolein is vasorelaxant at low levels (physiological) yet vasotoxic at high levels (toxicological).<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Subjects :
- Acetylcysteine blood
Acetylcysteine pharmacology
Acrolein blood
Animals
Aorta, Thoracic physiology
Female
GTPase-Activating Proteins genetics
GTPase-Activating Proteins physiology
Glutathione S-Transferase pi genetics
Glutathione S-Transferase pi physiology
Male
Mesenteric Artery, Superior physiology
Mice, Inbred C57BL
Mice, Knockout
TRPA1 Cation Channel genetics
Mice
Acetylcysteine analogs & derivatives
Acrolein pharmacology
Aorta, Thoracic drug effects
Mesenteric Artery, Superior drug effects
TRPA1 Cation Channel physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0333
- Volume :
- 426
- Database :
- MEDLINE
- Journal :
- Toxicology and applied pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 34271065
- Full Text :
- https://doi.org/10.1016/j.taap.2021.115647