Spontaneous coronary vasospasm in KATP mutant mice arises from a smooth muscle-extrinsic process

Rahul Kakkar, Bin Ye, Douglas A Stoller, Matthew Smelley, Nian Qing Shi, Kevin Galles, Michele Hadhazy, Jonathan C. Makielski, Elizabeth M. McNally

Research output: Contribution to journalArticle

59 Citations (Scopus)

Abstract

In the vasculature, ATP-sensitive potassium channels (KATP) channels regulate vascular tone. Mice with targeted gene disruptions of K ATP subunits expressed in vascular smooth muscle develop spontaneous coronary vascular spasm and sudden death. From these models, it was hypothesized that the loss of KATP channel activity in arterial vascular smooth muscle was responsible for coronary artery spasm. We now tested this hypothesis using a transgenic strategy where the full-length sulfonylurea receptor containing exon 40 was expressed under the control of a smooth muscle-specific SM22α promoter. Two transgenic founder lines were generated and independently bred to sulfonylurea receptor 2 (SUR2) null mice to generate mice that restored expression of KATP channels in vascular smooth muscle. Transgenic expression of the sulfonylurea receptor in vascular smooth muscle cells was confirmed by detecting mRNA and protein from the transgene. Functional restoration was determined by recording pinacidil-based KATP current by whole cell voltage clamping of isolated aortic vascular smooth muscle cells isolated from the transgenic restored mice. Despite successful restoration of KATP channels in vascular smooth muscle, transgene-restored SUR2 null mice continued to display frequent episodes of spontaneous ST segment elevation, identical to the phenotype seen in SUR2 null mice. As in SUR2 null mice, ST segment elevation was frequently followed by atrioventricular heart block. ST segment elevation and coronary perfusion pressure in the restored mice did not differ significantly between transgene-negative and transgene-positive SUR2 null mice. We conclude that spontaneous coronary vasospasm and sudden death in SUR2 null mice arises from a coronary artery vascular smooth muscle-extrinsic process.

Original languageEnglish (US)
Pages (from-to)682-689
Number of pages8
JournalCirculation Research
Volume98
Issue number5
DOIs
StatePublished - Mar 1 2006

Fingerprint

Coronary Vasospasm
Sulfonylurea Receptors
Smooth Muscle
Vascular Smooth Muscle
KATP Channels
Transgenes
Spasm
Sudden Death
Smooth Muscle Myocytes
Blood Vessels
Coronary Vessels
Pinacidil
Heart Block
Atrioventricular Block
Constriction
Transgenic Mice
Exons
Perfusion
Adenosine Triphosphate
Phenotype

Keywords

  • K channel
  • Smooth muscle
  • Sulfonylurea receptor
  • Vasospasm

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Spontaneous coronary vasospasm in KATP mutant mice arises from a smooth muscle-extrinsic process. / Kakkar, Rahul; Ye, Bin; Stoller, Douglas A; Smelley, Matthew; Shi, Nian Qing; Galles, Kevin; Hadhazy, Michele; Makielski, Jonathan C.; McNally, Elizabeth M.

In: Circulation Research, Vol. 98, No. 5, 01.03.2006, p. 682-689.

Research output: Contribution to journalArticle

Kakkar, R, Ye, B, Stoller, DA, Smelley, M, Shi, NQ, Galles, K, Hadhazy, M, Makielski, JC & McNally, EM 2006, 'Spontaneous coronary vasospasm in KATP mutant mice arises from a smooth muscle-extrinsic process', Circulation Research, vol. 98, no. 5, pp. 682-689. https://doi.org/10.1161/01.RES.0000207498.40005.e7
Kakkar, Rahul ; Ye, Bin ; Stoller, Douglas A ; Smelley, Matthew ; Shi, Nian Qing ; Galles, Kevin ; Hadhazy, Michele ; Makielski, Jonathan C. ; McNally, Elizabeth M. / Spontaneous coronary vasospasm in KATP mutant mice arises from a smooth muscle-extrinsic process. In: Circulation Research. 2006 ; Vol. 98, No. 5. pp. 682-689.
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