AI Article Synopsis

  • Hypertension is linked to older age and has been connected to the ATP2B1 gene, which affects blood pressure regulation.
  • Reduction of PMCA1 expression was studied in mice, revealing that normal blood pressure in young mice became significantly elevated in older mice (≥12 months).
  • Structural changes in small arteries occurred before blood pressure increased, suggesting that targeting PMCA1 could be a new strategy for managing high blood pressure in older individuals.

Article Abstract

Hypertension is a well-established risk factor for adverse cardiovascular events, and older age is a risk factor for the development of hypertension. Genomewide association studies have linked ATP2B1, the gene for the plasma membrane calcium ATPase 1 (PMCA1), to blood pressure (BP) and hypertension. Here, we present the effects of reduction in the expression of PMCA1 on BP and small artery structure and function when combined with advancing age. Heterozygous PMCA1 null mice (PMCA1 ) were generated and conscious BP was measured at 6 to 18 months of age. Passive and active properties of isolated small mesenteric arteries were examined by pressure myography. PMCA1 mice exhibited normal BP at 6 and 9 months of age but developed significantly elevated BP when compared to age-matched wild-type controls at ≥12 months of age. Decreased lumen diameter, increased wall thickness and increased wall:lumen ratio were observed in small mesenteric arteries from animals 9 months of age and older, indicative of eutrophic remodelling. Increases in mesenteric artery intrinsic tone and global intracellular calcium were evident in animals at both 6 and 18 months of age. Thus, decreased expression of PMCA1 is associated with increased BP when combined with advancing age. Changes in arterial structure precede the elevation of BP. Pathways involving PMCA1 may be a novel target for BP regulation in the elderly.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595685PMC
http://dx.doi.org/10.1111/acel.12637DOI Listing

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