ArticleThe Journal of physiology2003
Impaired arterial pressure regulation during exercise due to enhanced muscular vasodilatation in calponin knockout mice.
Article in The Journal of physiology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 17 citations in OpenAlex.
- Double deletion of calponin 1 and calponin 2 in mice decreases systemic blood pressure with blunted length-tension response of aortic smooth muscle.Journal of molecular and cellular cardiology · 2019Article
- Voluntary locomotion linked with cerebral activation is mediated by vasopressin V1a receptors in free-moving mice.The Journal of physiology · 2013Article
- Telemetric analysis of haemodynamic regulation during voluntary exercise training in mouse models.Experimental physiology · 2011Article
- Molecular regulation of contractile smooth muscle cell phenotype: implications for vascular tissue engineering.Tissue engineering. Part B, Reviews · 2010Review
- Increased cerebral activity suppresses baroreflex control of heart rate in freely moving mice.The Journal of physiology · 2009Article
- Smooth muscle signalling pathways in health and disease.Journal of cellular and molecular medicine · 2008Review
- Reduced alpha-adrenoceptor responsiveness and enhanced baroreflex sensitivity in Cry-deficient mice lacking a biological clock.The Journal of physiology · 2005Article
- Arterial baroreflex control of muscle blood flow at the onset of voluntary locomotion in mice.The Journal of physiology · 2003Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Calponin is known to be an actin binding protein in smooth muscle, inhibiting actomyosin ATPase activity in vitro. We previously reported that alpha-adrenergic vasoconstriction in calponin knockout (KO) mice was reduced compared with that in wild-type C57BL/6J (WT) mice and, as a compensation, arterial baroreflex sensitivity in KO mice was enhanced at rest. In the present study, we assessed arterial pressure regulation in WT and KO mice during graded treadmill exercise at 5, 10, and 15 m min-1. Mean arterial pressure (MAP) in KO mice fluctuated more than that in WT mice at every speed of exercise with two-fold higher variances (P < 0.001). The baroreflex sensitivity (Delta HR/Delta MAP) in WT mice (n = 6), determined from the heart rate response (Delta HR) to spontaneous change in MAP (Delta MAP), was -5.1 +/- 0.6 beats min-1 mmHg-1 (mean +/- S.E.M.) at rest and remained unchanged at -5.0 +/- 0.9 beats min-1 mmHg-1 during exercise (P < 0.01), while that in KO mice (n = 6) was -9.9 +/- 1.7 beats min-1 mmHg-1 at rest, significantly higher than that in WT mice (P < 0.001), and was reduced to -4.7 +/- 0.4 beats min-1 mmHg-1 during exercise (P < 0.01), not significantly different from that in WT mice. In another experiment, we measured muscle blood flow (MBF) in the thigh by laser-Doppler flowmetry, electromyogram (EMG), and MAP during voluntary locomotion in KO (n = 7) and WT (n = 7) mice. Muscle vascular conductance, MBF/MAP, started to increase immediately after locomotion, judged from EMG, and reached 50% of the maximum after the time of 2.3 +/- 0.2 s in KO mice, shorter than 5.8 +/- 0.6 s in WT mice (P < 0.001). Prior administration of alpha-adrenergic blockade (phentolamine) shortened the time in WT mice to that in KO mice (P < 0.001), but did not shorten the time in KO mice. Thus, impaired MAP regulation in KO mice during exercise was caused by a blunted muscle vascular alpha-adrenergic contractile response and by the attenuated HR response to spontaneous change in MAP due to reduced baroreflex sensitivity.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.