Chemerin is resident to vascular tunicas and contributes to vascular tone.


Journal

American journal of physiology. Heart and circulatory physiology
ISSN: 1522-1539
Titre abrégé: Am J Physiol Heart Circ Physiol
Pays: United States
ID NLM: 100901228

Informations de publication

Date de publication:
01 07 2023
Historique:
medline: 28 6 2023
pubmed: 9 6 2023
entrez: 9 6 2023
Statut: ppublish

Résumé

The adipokine chemerin may support blood pressure, evidenced by a fall in mean arterial pressure after whole body antisense oligonucleotide (ASO)-mediated knockdown of chemerin protein in rat models of normal and elevated blood pressure. Although the liver is the greatest contributor of circulating chemerin, liver-specific ASOs that abolished hepatic-derived chemerin did not change blood pressure. Thus, other sites must produce the chemerin that supports blood pressure. We hypothesize that the vasculature is a source of chemerin independent of the liver that supports arterial tone. RNAScope, PCR, Western blot analyses, ASOs, isometric contractility, and radiotelemetry were used in the Dahl salt-sensitive (SS) rat (male and female) on a normal diet. Retinoic acid receptor responder 2 (

Identifiants

pubmed: 37294893
doi: 10.1152/ajpheart.00239.2023
doi:

Substances chimiques

Rarres2 protein, rat 0
Chemokines 0

Banques de données

figshare
['10.6084/m9.figshare.22692973.v1']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

H172-H186

Commentaires et corrections

Type : CommentIn

Auteurs

Emma Wabel (E)

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.

Alexis Orr (A)

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.

Emma D Flood (ED)

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.

Janice M Thompson (JM)

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.

Huirong Xie (H)

Transgenic and Genome Editing Facility, Research Technology Support Facility, and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan, United States.

Elena Y Demireva (EY)

Transgenic and Genome Editing Facility, Research Technology Support Facility, and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan, United States.

Bana Abolibdeh (B)

Transgenic and Genome Editing Facility, Research Technology Support Facility, and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan, United States.

Darcy Honke Hulbert (D)

Cardiovascular Division, Campus Animal Resources, Michigan State University, East Lansing, Michigan, United States.

Adam E Mullick (AE)

Ionis Pharmaceuticals, Carlsbad, California, United States.

Hannah Garver (H)

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.

Gregory D Fink (GD)

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.

Theodore A Kung (TA)

Section of Plastic and Reconstructive Surgery, Department of Surgery, Michigan Medicine, Ann Arbor, Michigan, United States.

Stephanie W Watts (SW)

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.

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Classifications MeSH