Rat arterial smooth muscle devoid of ryanodine receptor function: effects on cellular Ca2+ handling
(2001) In British Journal of Pharmacology 132(8). p.1957-1966- Abstract
- The roles of intracellular Ca2+ stores and ryanodine (Ry) receptors for vascular Ca2+ homeostasis and viability were investigated in rat tail arterial segments kept in organ culture with Ry (10 100 M) for up to 4 days. Acute exposure to Ry or the non-deactivating ryanodine analogue C10-Oeq glycyl ryanodine (10 M) eliminated Ca2+ release responses to caffeine (20 mM) and noradrenaline (NA, 10 M), whereas responses to NA, but not caffeine, gradually returned to normal within 4 days of exposure to Ry. Ry receptor protein was detected on Western blots in arteries cultured either with or without Ry. Brief Ca2+ release events (sparks) were absent after culture with Ry, whereas Ca2+ waves still occurred. The propagation velocity of waves was... (More)
- The roles of intracellular Ca2+ stores and ryanodine (Ry) receptors for vascular Ca2+ homeostasis and viability were investigated in rat tail arterial segments kept in organ culture with Ry (10 100 M) for up to 4 days. Acute exposure to Ry or the non-deactivating ryanodine analogue C10-Oeq glycyl ryanodine (10 M) eliminated Ca2+ release responses to caffeine (20 mM) and noradrenaline (NA, 10 M), whereas responses to NA, but not caffeine, gradually returned to normal within 4 days of exposure to Ry. Ry receptor protein was detected on Western blots in arteries cultured either with or without Ry. Brief Ca2+ release events (sparks) were absent after culture with Ry, whereas Ca2+ waves still occurred. The propagation velocity of waves was equal (19 m s-1) in tissue cultured either with or without Ry. Inhibition of Ca2+ accumulation into the sarcoplasmic reticulum (SR) by culture with caffeine (5 mM), cyclopiazonic acid or thapsigargin (both 10 M) decreased contractility due to Ca2+-induced cell damage. In contrast, culture with Ry did not affect contractility. Removal of Ca2+ from the cytosol following a Ca2+ load was retarded after Ry culture. Thapsigargin reduced the rate of Ca2+ removal in control cultured rings, but had no effect after Ry culture. It is concluded that intracellular Ca2+ stores recover during chronic Ry treatment, while Ry receptors remain non-functional. Ry receptor activity is required for Ca2+ sparks and for SR-dependent recovery from a Ca2+ load, but not for Ca2+ waves or basal Ca2+ homeostasis. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/131318
- author
- Dreja, Karl LU ; Nordström, Ina LU and Hellstrand, Per LU
- organization
- publishing date
- 2001
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Ryanodine receptors, smooth muscle, Ca2+ stores, sarcoplasmic reticulum, organ culture, Ca2+ sparks, Ca2+ waves
- in
- British Journal of Pharmacology
- volume
- 132
- issue
- 8
- pages
- 1957 - 1966
- publisher
- Wiley
- external identifiers
-
- wos:000168326100038
- pmid:11309269
- scopus:0035041734
- ISSN
- 1476-5381
- DOI
- 10.1038/sj.bjp.0703986
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Unit on Vascular Diabetic Complications (013241510), Vascular Physiology (013212034), Cellular Biomechanics (013212075)
- id
- f575a5a8-dfd8-444e-b4d9-1276c8d9e5a6 (old id 131318)
- date added to LUP
- 2016-04-01 16:24:37
- date last changed
- 2022-04-22 21:51:49
@article{f575a5a8-dfd8-444e-b4d9-1276c8d9e5a6, abstract = {{The roles of intracellular Ca2+ stores and ryanodine (Ry) receptors for vascular Ca2+ homeostasis and viability were investigated in rat tail arterial segments kept in organ culture with Ry (10 100 M) for up to 4 days. Acute exposure to Ry or the non-deactivating ryanodine analogue C10-Oeq glycyl ryanodine (10 M) eliminated Ca2+ release responses to caffeine (20 mM) and noradrenaline (NA, 10 M), whereas responses to NA, but not caffeine, gradually returned to normal within 4 days of exposure to Ry. Ry receptor protein was detected on Western blots in arteries cultured either with or without Ry. Brief Ca2+ release events (sparks) were absent after culture with Ry, whereas Ca2+ waves still occurred. The propagation velocity of waves was equal (19 m s-1) in tissue cultured either with or without Ry. Inhibition of Ca2+ accumulation into the sarcoplasmic reticulum (SR) by culture with caffeine (5 mM), cyclopiazonic acid or thapsigargin (both 10 M) decreased contractility due to Ca2+-induced cell damage. In contrast, culture with Ry did not affect contractility. Removal of Ca2+ from the cytosol following a Ca2+ load was retarded after Ry culture. Thapsigargin reduced the rate of Ca2+ removal in control cultured rings, but had no effect after Ry culture. It is concluded that intracellular Ca2+ stores recover during chronic Ry treatment, while Ry receptors remain non-functional. Ry receptor activity is required for Ca2+ sparks and for SR-dependent recovery from a Ca2+ load, but not for Ca2+ waves or basal Ca2+ homeostasis.}}, author = {{Dreja, Karl and Nordström, Ina and Hellstrand, Per}}, issn = {{1476-5381}}, keywords = {{Ryanodine receptors; smooth muscle; Ca2+ stores; sarcoplasmic reticulum; organ culture; Ca2+ sparks; Ca2+ waves}}, language = {{eng}}, number = {{8}}, pages = {{1957--1966}}, publisher = {{Wiley}}, series = {{British Journal of Pharmacology}}, title = {{Rat arterial smooth muscle devoid of ryanodine receptor function: effects on cellular Ca2+ handling}}, url = {{https://lup.lub.lu.se/search/files/4664422/624195.pdf}}, doi = {{10.1038/sj.bjp.0703986}}, volume = {{132}}, year = {{2001}}, }