Literature DB >> 9180637

Effects of age on Ca2+ currents in small mesenteric artery myocytes from Wistar-Kyoto and spontaneously hypertensive rats.

I M Lozinskaya1, R H Cox.   

Abstract

The purpose of this study was to test the hypothesis that differences in voltage-gated Ca2+ channels increase with age during the development of sustained hypertension in the spontaneously hypertensive rat (SHR). Using patch-clamp methods, we measured whole-cell Ca2+ currents in freshly isolated myocytes from small mesenteric arteries of juvenile (5 to 7 weeks), young (10 to 12 weeks), and mature (19 to 23 weeks) Wistar-Kyoto rats (WKY) and SHR. Indirect tail artery systolic pressure increased progressively with age in SHR (from 125 +/- 5 to 159 +/- 5 to 192 +/- 5 mm Hg) but only in the younger WKY (from 107 +/- 6 to 130 +/- 4 to 136 +/- 4 mm Hg). Peak Ca2+ current density (current per cell capacitance) was larger in SHR than WKY myocytes at all ages (at 6 weeks, 3.5 +/- 0.4 versus 2.3 +/- 0.2 pA/pF; at 12 weeks, 3.8 +/- 0.2 versus 3.1 +/- 0.2; at 20 weeks. 4.9 +/- 0.4 versus 3.3 +/- 0.4). Cell capacitance (surface area) was significantly smaller in 12-week-old SHR than WKY (25.2 +/- 1.1 versus 31.8 +/- 1.6 pF), but no differences were found in the 6- or 20-week-old groups. There were significant differences in Ca2+ current with strain, age, and voltage but no significant age-strain interactions. The ratio of peak Ca2+ current for SHR to that of WKY declined linearly with voltage at all ages suggesting differences in the voltage dependence of Ca2+ current activation. The voltage dependence of Ca2+ current was shifted to the left in SHR compared with WKY at all ages. Activation curves were shifted significantly in the negative-voltage direction only in 20-week-old SHR myocytes. We have found differences with age in Ca2+ current density and its voltage dependence in SHR compared with WKY during the phase of development in which blood pressure becomes established in the SHR. The net effect of these differences predicts a larger Ca2+ current in SHR at voltages in the physiological range of membrane potential.

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Year:  1997        PMID: 9180637     DOI: 10.1161/01.hyp.29.6.1329

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  14 in total

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2.  Disrupting calcium channel expression to lower blood pressure: new targeting of a well-known channel.

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Journal:  Mol Interv       Date:  2006-12

3.  Vascular smooth muscle-specific knockdown of the noncardiac form of the L-type calcium channel by microRNA-based short hairpin RNA as a potential antihypertensive therapy.

Authors:  Sung W Rhee; Joseph R Stimers; Wenze Wang; Li Pang
Journal:  J Pharmacol Exp Ther       Date:  2009-02-24       Impact factor: 4.030

4.  Exercise intensity-dependent reverse and adverse remodeling of voltage-gated Ca(2+) channels in mesenteric arteries from spontaneously hypertensive rats.

Authors:  Yu Chen; Hanmeng Zhang; Yanyan Zhang; Ni Lu; Lin Zhang; Lijun Shi
Journal:  Hypertens Res       Date:  2015-04-23       Impact factor: 3.872

5.  Expression of Calcium Channel Subunit Variants in Small Mesenteric Arteries of WKY and SHR.

Authors:  Robert H Cox; Samantha Fromme
Journal:  Am J Hypertens       Date:  2015-03-28       Impact factor: 2.689

6.  Chronic exercise normalizes changes in Cav 1.2 and KCa 1.1 channels in mesenteric arteries from spontaneously hypertensive rats.

Authors:  Lijun Shi; Hanmeng Zhang; Yu Chen; Yujia Liu; Ni Lu; Tengteng Zhao; Lubo Zhang
Journal:  Br J Pharmacol       Date:  2015-01-23       Impact factor: 8.739

Review 7.  Ion channel remodeling in vascular smooth muscle during hypertension: Implications for novel therapeutic approaches.

Authors:  Biny K Joseph; Keshari M Thakali; Christopher L Moore; Sung W Rhee
Journal:  Pharmacol Res       Date:  2013-01-31       Impact factor: 7.658

8.  Vascular mineralocorticoid receptor regulates microRNA-155 to promote vasoconstriction and rising blood pressure with aging.

Authors:  Jennifer J DuPont; Amy McCurley; Ana P Davel; Joseph McCarthy; Shawn B Bender; Kwangseok Hong; Yan Yang; Jeung-Ki Yoo; Mark Aronovitz; Wendy E Baur; Demetra D Christou; Michael A Hill; Iris Z Jaffe
Journal:  JCI Insight       Date:  2016-09-08

9.  A naturally occurring truncated Cav1.2 α1-subunit inhibits Ca2+ current in A7r5 cells.

Authors:  Robert H Cox; Samantha J Fromme
Journal:  Am J Physiol Cell Physiol       Date:  2013-08-07       Impact factor: 4.249

10.  Down-regulation of CaV1.2 channels during hypertension: how fewer CaV1.2 channels allow more Ca(2+) into hypertensive arterial smooth muscle.

Authors:  Sendoa Tajada; Pilar Cidad; Olaia Colinas; L Fernando Santana; José R López-López; M Teresa Pérez-García
Journal:  J Physiol       Date:  2013-10-28       Impact factor: 5.182

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