Vascular dysfunction precedes hypertension associated with a blood pressure locus on rat chromosome 12

Sasha Z. Prisco, Jessica R.C. Priestley, Brian D. Weinberg, Anthony R. Prisco, Matthew J. Hoffman, Howard J. Jacob, Michael J. Flister, Julian H. Lombard, Jozef Lazar

Research output: Contribution to journalArticlepeer-review

1 Scopus citations


We previously isolated a 6.1-Mb region of SS/Mcwi (Dahl salt-sensitive) rat chromosome 12 (13.4–19.5 Mb) that significantly elevated blood pressure (BP) (Δ+34 mmHg, P < 0.001) compared with the SS-12BN consomic control. In the present study, we examined the role of vascular dysfunction and remodeling in hypertension risk associated with the 6.1-Mb (13.4–19.5 Mb) locus on rat chromosome 12 by reducing dietary salt, which lowered BP levels so that there were no substantial differences in BP between strains. Consequently, any observed differences in the vasculature were considered BP-independent. We also reduced the candidate region from 6.1 Mb with 133 genes to 2 Mb with 23 genes by congenic mapping. Both the 2 Mb and 6.1 Mb congenic intervals were associated with hypercontractility and decreased elasticity of resistance vasculature prior to elevations of BP, suggesting that the vascular remodeling and dysfunction likely contribute to the pathogenesis of hypertension in these congenic models. Of the 23 genes within the narrowed congenic interval, 12 were differentially expressed between the resistance vasculature of the 2 Mb congenic and SS-12BNconsomic strains. Among these, Grifin was consistently upregulated 2.7 ± 0.6-fold (P < 0.05) and 2.0 ± 0.3-fold (P < 0.01), and Chst12 was consistently downregulated −2.8 ± 0.3-fold (P < 0.01) and −4.4 ± 0.4-fold (P< 0.00001) in the 2 Mb congenic compared with SS-12BN consomic under normotensive and hypertensive conditions, respectively. A syntenic region on human chromosome 7 has also been associated with BP regulation, suggesting that identification of the genetic mechanism(s) underlying cardiovascular phenotypes in this congenic strain will likely be translated to a better understanding of human hypertension.

Original languageEnglish (US)
Pages (from-to)H1103-H1110
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Issue number8
StatePublished - Oct 15 2014

Bibliographical note

Publisher Copyright:
© 2014 the American Physiological Society.


  • Brown Norway
  • Dahl salt-sensitive
  • Genetic
  • Vessel


Dive into the research topics of 'Vascular dysfunction precedes hypertension associated with a blood pressure locus on rat chromosome 12'. Together they form a unique fingerprint.

Cite this