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Perivascular adipose tissue remodeling impairs vasoreactivity in thermoneutral-housed rats.
Henckel, Melissa M; Chun, Ji Hye; Knaub, Leslie A; Pott, Gregory B; James, Georgia E; Hunter, Kendall S; Shandas, Robin; Walker, Lori A; Reusch, Jane E-B; Keller, Amy C.
Afiliación
  • Henckel MM; Division of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.
  • Chun JH; Rocky Mountain Regional VA Medical Center, Aurora, CO 80045.
  • Knaub LA; Division of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.
  • Pott GB; Rocky Mountain Regional VA Medical Center, Aurora, CO 80045.
  • James GE; Division of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.
  • Hunter KS; Rocky Mountain Regional VA Medical Center, Aurora, CO 80045.
  • Shandas R; Division of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.
  • Walker LA; Rocky Mountain Regional VA Medical Center, Aurora, CO 80045.
  • Reusch JE; University of Iowa, Iowa City, IA 52242.
  • Keller AC; Department of Bioengineering, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.
bioRxiv ; 2024 May 13.
Article en En | MEDLINE | ID: mdl-38798439
ABSTRACT

Objective:

Vascular pathology, characterized by impaired vasoreactivity and mitochondrial respiration, differs between the sexes. Housing rats under thermoneutral (TN) conditions causes vascular dysfunction and perturbed metabolism. We hypothesized that perivascular adipose tissue (PVAT), a vasoregulatory adipose depot with brown adipose tissue (BAT) phenotype, remodels to a white adipose (WAT) phenotype in rats housed at TN, driving diminished vasoreactivity in a sex-dependent manner.

Methods:

Male and female Wistar rats were housed at either room temperature (RT) or TN. Endpoints included changes in PVAT morphology, vasoreactivity in vessels with intact PVAT or transferred to PVAT of the oppositely-housed animal, vessel stiffness, vessel mitochondrial respiration and cellular signaling.

Results:

Remodeling of PVAT was observed in rats housed at TN; animals in this environment showed PVAT whitening and displayed diminished aortae vasodilation (p<0.05), different between the sexes. Juxtaposing PVAT from RT rats onto aortae from TN rats in females corrected vasodilation (p<0.05); this did not occur in males. In aortae of all animals housed at TN, mitochondrial respiration was significantly diminished in lipid substrate experiments (p<0.05), and there was significantly less expression of peNOS (p<0.001).

Conclusions:

These data are consistent with TN-induced remodeling of PVAT, notably associated with sex-specific blunting of vasoreactivity, diminished mitochondrial respiration, and altered cellular signaling.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article