Differential modulation of caffeine- and IP3-induced calcium release in cultured arterial tissue
(1999) In American Journal of Physiology: Cell Physiology 276(5). p.1115-1120- Abstract
- To investigate the Ca2+-dependent plasticity of sarcoplasmic reticulum (SR) function in vascular smooth muscle, transient responses to agents releasing intracellular Ca2+ by either ryanodine (caffeine) or D-myo-inositol 1,4,5-trisphosphate [IP3; produced in response to norepinephrine (NE), 5-hydroxytryptamine (5-HT), arginine vasopressin (AVP)] receptors in rat tail arterial rings were evaluated after 4 days of organ culture. Force transients induced by all agents were increased compared with those induced in fresh rings. Stimulation by 10% FCS during culture further potentiated the force and Ca2+ responses to caffeine (20 mM) but not to NE (10 microM), 5-HT (10 microM), or AVP (0.1 microM). The effect was persistent, and SR capacity was... (More)
- To investigate the Ca2+-dependent plasticity of sarcoplasmic reticulum (SR) function in vascular smooth muscle, transient responses to agents releasing intracellular Ca2+ by either ryanodine (caffeine) or D-myo-inositol 1,4,5-trisphosphate [IP3; produced in response to norepinephrine (NE), 5-hydroxytryptamine (5-HT), arginine vasopressin (AVP)] receptors in rat tail arterial rings were evaluated after 4 days of organ culture. Force transients induced by all agents were increased compared with those induced in fresh rings. Stimulation by 10% FCS during culture further potentiated the force and Ca2+ responses to caffeine (20 mM) but not to NE (10 microM), 5-HT (10 microM), or AVP (0.1 microM). The effect was persistent, and SR capacity was not altered after reversible depletion of stores with cyclopiazonic acid. The effects of serum could be mimicked by culture in depolarizing medium (30 mM K+) and blocked by the addition of verapamil (1 microM) or EGTA (1 mM) to the medium, lowering intracellular Ca2+ concentration ([Ca2+]i) during culture. These results show that modulation of SR function can occur in vitro by a mechanism dependent on long-term levels of basal [Ca2+]i and involving ryanodine- but not IP3 receptor-mediated Ca2+ release. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1114548
- author
- Dreja, Karl LU and Hellstrand, Per LU
- organization
- publishing date
- 1999
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- sarcoplasmic reticulum, organ culture, tail artery, D-myo-inositol 1, 4, 5-trisphosphate
- in
- American Journal of Physiology: Cell Physiology
- volume
- 276
- issue
- 5
- pages
- 1115 - 1120
- publisher
- American Physiological Society
- external identifiers
-
- pmid:10329960
- ISSN
- 1522-1563
- language
- English
- LU publication?
- yes
- id
- bff1db48-2211-4484-bcc6-cddfd1ab77eb (old id 1114548)
- alternative location
- http://ajpcell.physiology.org/cgi/content/full/276/5/C1115
- date added to LUP
- 2016-04-01 16:06:01
- date last changed
- 2020-09-16 15:40:22
@article{bff1db48-2211-4484-bcc6-cddfd1ab77eb, abstract = {{To investigate the Ca2+-dependent plasticity of sarcoplasmic reticulum (SR) function in vascular smooth muscle, transient responses to agents releasing intracellular Ca2+ by either ryanodine (caffeine) or D-myo-inositol 1,4,5-trisphosphate [IP3; produced in response to norepinephrine (NE), 5-hydroxytryptamine (5-HT), arginine vasopressin (AVP)] receptors in rat tail arterial rings were evaluated after 4 days of organ culture. Force transients induced by all agents were increased compared with those induced in fresh rings. Stimulation by 10% FCS during culture further potentiated the force and Ca2+ responses to caffeine (20 mM) but not to NE (10 microM), 5-HT (10 microM), or AVP (0.1 microM). The effect was persistent, and SR capacity was not altered after reversible depletion of stores with cyclopiazonic acid. The effects of serum could be mimicked by culture in depolarizing medium (30 mM K+) and blocked by the addition of verapamil (1 microM) or EGTA (1 mM) to the medium, lowering intracellular Ca2+ concentration ([Ca2+]i) during culture. These results show that modulation of SR function can occur in vitro by a mechanism dependent on long-term levels of basal [Ca2+]i and involving ryanodine- but not IP3 receptor-mediated Ca2+ release.}}, author = {{Dreja, Karl and Hellstrand, Per}}, issn = {{1522-1563}}, keywords = {{sarcoplasmic reticulum; organ culture; tail artery; D-myo-inositol 1; 4; 5-trisphosphate}}, language = {{eng}}, number = {{5}}, pages = {{1115--1120}}, publisher = {{American Physiological Society}}, series = {{American Journal of Physiology: Cell Physiology}}, title = {{Differential modulation of caffeine- and IP3-induced calcium release in cultured arterial tissue}}, url = {{http://ajpcell.physiology.org/cgi/content/full/276/5/C1115}}, volume = {{276}}, year = {{1999}}, }