Alkylacetylglycerophosphocholine stimulates Na + -Ca 2+ exchange, protein phosphorylation and polyphosphoinositide turnover in rat ileal plasmalemmal vesicles
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, ISSN: 0167-4889, Vol: 888, Issue: 3, Page: 306-315
1986
- 10Citations
- 1Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations10
- Citation Indexes10
- 10
- CrossRef7
- Captures1
- Readers1
Article Description
The novel ether phospholipid, 1- O -alkyl-2-acetyl- sn -glycero-3-phosphocholine (AGEPC), isometrically contracted helically cut rat ileal smooth muscle strips in a dose- and time-dependent manner. Utilizing an enriched plasma membrane vesicular preparation from rat ileal longitudinal smooth muscle, AGEPC specifically stimulated Na + -Ca 2+ exchange in a dose- and time-dependent manner. Concomitant with the AGEPC stimulation of Na + -dependent Ca 2+ influx in plasma membrane vesicles is an enhanced turnover of the polyphosphoinositides, an elevated concentration of phosphatidic acid and also an enhanced phosphorylation of an M r 40 000 plasmalemmal protein. The mechanisms by which AGEPC may regulate ileal plasmalemmal Ca 2+ flux and contractility are considered.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0167488986902302; http://dx.doi.org/10.1016/0167-4889(86)90230-2; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0022473482&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/3019423; https://linkinghub.elsevier.com/retrieve/pii/0167488986902302; http://dx.doi.org/10.1016/0167-4889%2886%2990230-2; https://dx.doi.org/10.1016/0167-4889%2886%2990230-2
Elsevier BV
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