Senescent murine femoral arteries undergo vascular remodelling associated with accelerated stress-induced contractility and reactivity to nitric oxide

Basic Clin Pharmacol Toxicol. 2022 Jan;130(1):70-83. doi: 10.1111/bcpt.13675. Epub 2021 Nov 11.

Abstract

This work explored the mechanism of augmented stress-induced vascular reactivity of senescent murine femoral arteries (FAs). Mechanical and pharmacological reactivity of young (12-25 weeks, y-FA) and senescent (>104 weeks, s-FAs) femoral arteries was measured by wire myography. Expression and protein phosphorylation of selected regulatory proteins were studied by western blotting. Expression ratio of the Exon24 in/out splice isoforms of the regulatory subunit of myosin phosphatase, MYPT1 (MYPT1-Exon24 in/out), was determined by polymerase chain reaction (PCR). While the resting length-tension relationship showed no alteration, the stretch-induced-tone increased to 8.3 ± 0.9 mN in s-FA versus only 4.6 ± 0.3 mN in y-FAs. Under basal conditions, phosphorylation of the regulatory light chain of myosin at S19 was 19.2 ± 5.8% in y-FA versus 49.2 ± 12.6% in s-FA. Inhibition of endogenous NO release raised tone additionally to 10.4 ± 1.2 mN in s-FA, whereas this treatment had a negligible effect in y-FAs (4.8 ± 0.3 mN). In s-FAs, reactivity to NO donor was augmented (pD2 = -4.5 ± 0.3 in y-FA vs. -5.2 ± 0.1 in senescent). Accordingly, in s-FAs, MYPT1-Exon24-out-mRNA, which is responsible for expression of the more sensitive to protein-kinase G, leucine-zipper-positive MYPT1 isoform, was increased. The present work provides evidence that senescent murine s-FA undergoes vascular remodelling associated with increases in stretch-activated contractility and sensitivity to NO/cGMP/PKG system.

Keywords: ageing; cardiovascular pharmacology; hypertension; reproductive and developmental toxicology.

MeSH terms

  • Age Factors
  • Animals
  • Cyclic GMP / metabolism
  • Cyclic GMP-Dependent Protein Kinases / metabolism
  • Femoral Artery / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Myosin-Light-Chain Phosphatase / metabolism
  • Nitric Oxide / metabolism*
  • Nitric Oxide Donors / pharmacology
  • Phosphorylation
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Stress, Physiological / physiology*
  • Vascular Remodeling / physiology*
  • Vascular Stiffness / physiology

Substances

  • Nitric Oxide Donors
  • RNA, Messenger
  • Nitric Oxide
  • Cyclic GMP-Dependent Protein Kinases
  • Myosin-Light-Chain Phosphatase
  • Ppp1r12a protein, mouse
  • Cyclic GMP