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- Publisher Website: 10.1152/ajpcell.00534.2002
- Scopus: eid_2-s2.0-0242426654
- PMID: 14600077
- WOS: WOS:000186343600008
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Article: Calcium homeostasis in rat cardiomyocytes during chronic hypoxia: A time course study
Title | Calcium homeostasis in rat cardiomyocytes during chronic hypoxia: A time course study |
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Authors | |
Keywords | β-adrenoceptor Calcium-adenosine-triphosphatase Chronic hypoxia Intracellular calcium ion concentration Ryanodine receptor Sarcoplasmic reticulum Sodium/calcium exchange |
Issue Date | 2003 |
Publisher | American Physiological Society. The Journal's web site is located at http://intl-ajpcell.physiology.org/ |
Citation | American Journal Of Physiology - Cell Physiology, 2003, v. 285 n. 6 54-6, p. C1420-C1428 How to Cite? |
Abstract | The present study determined Ca2+ handling in the hearts of rats subjected to chronic hypoxia (CH). Spectrofluorometry was used to measure intracellular Ca2+ concentration ([Ca2+]i) and its responses to electrical stimulation, caffeine, and isoproterenol in myocytes from the right ventricle of rats breathing 10% oxygen for 1, 3, 7, 14, 21, 28, and 56 days and age-matched controls. The protein expression of sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) and its ryanodine receptor (RyR) were measured. The uptake of 45Ca2+ by SERCA, release by RyR, and extrusion by Na+/Ca2+ exchange (NCX) were determined. It was found that Ca2+ homeostasis and Ca 2+ responses to β-adrenoceptor stimulation reached a new equilibrium after 4 wk of CH. Ca2+ content in the sarcoplasmic reticulum (SR) was reduced, but cytosolic Ca2+ remained unchanged after CH. Expression of SERCA and its Ca2+ uptake, Ca2+ release via RyR, and NCX activity were suppressed by CH. The results indicate impaired Ca2+ handling, which may be responsible for the attenuated Ca2+ responses to β-adrenoceptor stimulation in CH. |
Persistent Identifier | http://hdl.handle.net/10722/171718 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 1.711 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Pei, JM | en_US |
dc.contributor.author | Kravtsov, GM | en_US |
dc.contributor.author | Wu, S | en_US |
dc.contributor.author | Das, R | en_US |
dc.contributor.author | Fung, ML | en_US |
dc.contributor.author | Wong, TM | en_US |
dc.date.accessioned | 2012-10-30T06:16:35Z | - |
dc.date.available | 2012-10-30T06:16:35Z | - |
dc.date.issued | 2003 | en_US |
dc.identifier.citation | American Journal Of Physiology - Cell Physiology, 2003, v. 285 n. 6 54-6, p. C1420-C1428 | en_US |
dc.identifier.issn | 0363-6143 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/171718 | - |
dc.description.abstract | The present study determined Ca2+ handling in the hearts of rats subjected to chronic hypoxia (CH). Spectrofluorometry was used to measure intracellular Ca2+ concentration ([Ca2+]i) and its responses to electrical stimulation, caffeine, and isoproterenol in myocytes from the right ventricle of rats breathing 10% oxygen for 1, 3, 7, 14, 21, 28, and 56 days and age-matched controls. The protein expression of sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) and its ryanodine receptor (RyR) were measured. The uptake of 45Ca2+ by SERCA, release by RyR, and extrusion by Na+/Ca2+ exchange (NCX) were determined. It was found that Ca2+ homeostasis and Ca 2+ responses to β-adrenoceptor stimulation reached a new equilibrium after 4 wk of CH. Ca2+ content in the sarcoplasmic reticulum (SR) was reduced, but cytosolic Ca2+ remained unchanged after CH. Expression of SERCA and its Ca2+ uptake, Ca2+ release via RyR, and NCX activity were suppressed by CH. The results indicate impaired Ca2+ handling, which may be responsible for the attenuated Ca2+ responses to β-adrenoceptor stimulation in CH. | en_US |
dc.language | eng | en_US |
dc.publisher | American Physiological Society. The Journal's web site is located at http://intl-ajpcell.physiology.org/ | en_US |
dc.relation.ispartof | American Journal of Physiology - Cell Physiology | en_US |
dc.subject | β-adrenoceptor | - |
dc.subject | Calcium-adenosine-triphosphatase | - |
dc.subject | Chronic hypoxia | - |
dc.subject | Intracellular calcium ion concentration | - |
dc.subject | Ryanodine receptor | - |
dc.subject | Sarcoplasmic reticulum | - |
dc.subject | Sodium/calcium exchange | - |
dc.subject.mesh | Adrenergic Beta-Agonists - Pharmacology | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Anoxia - Metabolism | en_US |
dc.subject.mesh | Caffeine - Pharmacology | en_US |
dc.subject.mesh | Calcium - Analysis - Metabolism | en_US |
dc.subject.mesh | Calcium-Transporting Atpases - Biosynthesis - Drug Effects | en_US |
dc.subject.mesh | Cells, Cultured | en_US |
dc.subject.mesh | Central Nervous System Stimulants - Pharmacology | en_US |
dc.subject.mesh | Electric Stimulation | en_US |
dc.subject.mesh | Homeostasis - Physiology | en_US |
dc.subject.mesh | Intracellular Fluid - Chemistry - Drug Effects | en_US |
dc.subject.mesh | Isoproterenol - Pharmacology | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Myocytes, Cardiac - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Sprague-Dawley | en_US |
dc.subject.mesh | Ryanodine Receptor Calcium Release Channel - Biosynthesis - Drug Effects | en_US |
dc.subject.mesh | Sarcoplasmic Reticulum - Metabolism | en_US |
dc.subject.mesh | Sarcoplasmic Reticulum Calcium-Transporting Atpases | en_US |
dc.subject.mesh | Sodium-Calcium Exchanger - Metabolism | en_US |
dc.subject.mesh | Spectrometry, Fluorescence | en_US |
dc.subject.mesh | Time Factors | en_US |
dc.title | Calcium homeostasis in rat cardiomyocytes during chronic hypoxia: A time course study | en_US |
dc.type | Article | en_US |
dc.identifier.email | Fung, ML:fungml@hkucc.hku.hk | en_US |
dc.identifier.email | Kravtsov, GM: gmkravts@HKUCC.hku.hk | - |
dc.identifier.email | Das, R: raptidas@hkucc.hku.hk | - |
dc.identifier.email | Wong, TM: tm.wong@hkuspace.hku.hk | - |
dc.identifier.authority | Fung, ML=rp00433 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1152/ajpcell.00534.2002 | - |
dc.identifier.pmid | 14600077 | - |
dc.identifier.scopus | eid_2-s2.0-0242426654 | en_US |
dc.identifier.hkuros | 88098 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0242426654&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 285 | en_US |
dc.identifier.issue | 6 54-6 | en_US |
dc.identifier.spage | C1420 | en_US |
dc.identifier.epage | C1428 | en_US |
dc.identifier.isi | WOS:000186343600008 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Pei, JM=7103299061 | en_US |
dc.identifier.scopusauthorid | Kravtsov, GM=7003811092 | en_US |
dc.identifier.scopusauthorid | Wu, S=7408443898 | en_US |
dc.identifier.scopusauthorid | Das, R=7202061890 | en_US |
dc.identifier.scopusauthorid | Fung, ML=7101955092 | en_US |
dc.identifier.scopusauthorid | Wong, TM=7403531434 | en_US |
dc.identifier.issnl | 0363-6143 | - |