Daniel Potreau
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Daniel Potreau has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
Guy Raymond
Institut de Physiologie et de Biologie Cellulaires, UMR 6187, 40 avenue du Recteur Pineau, 86022 Poitiers Cedex, France
2 shared publicationsJocelyn Bescond
Institut de Physiologie et Biologie Cellulaires, Université de Poitiers, CNRS UMR 6187, 40 Avenue du Recteur Pineau, 86022 Poitiers Cedex, France
2 shared publicationsAmani Cheikh
Laboratoire Venins et Toxines, Institut Pasteur de Tunis, BP 74-1002, Tunis, Tunisia
1 shared publicationChristian Cognard
Institut de Physiologie et de Biologie Cellulaires, UMR 6187, 40 avenue du Recteur Pineau, 86022 Poitiers Cedex, France
1 shared publication- Christian Cognard
Institut de Physiologie et de Biologie Cellulaires, UMR 6187, 40 avenue du Recteur Pineau, Poitiers Cedex 86022, France
1 shared publication - Claire Louault
Institut de Physiologie et Biologie Cellulaires, Université de Poitiers, CNRS UMR 6187, 40 Avenue du Recteur Pineau, 86022 Poitiers Cedex, France
1 shared publication
Latest Publications
- 1 October 2008
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Biomembranes
- Vol. 1778 (10) , 2097-2104
Implication of connexins 40 and 43 in functional coupling between mouse cardiac fibroblasts in primary culture
- 1 October 2008
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Biomembranes
- Vol. 1778 (10) , 2097-2104
Implication of connexins 40 and 43 in functional coupling between mouse cardiac fibroblasts in primary culture
- 1 April 1987
- Published by Canadian Science Publishing in Canadian Journal of Physiology and Pharmacology
- Vol. 65 (4) , 704-710
Stimulation frequency and external ionic composition control the repriming of caffeine-induced contractures in frog skeletal muscle
The effect of stimulation rate and of external ionic composition on the repriming period of contractures induced by 6 mM caffeine was tested on isolated skeletal muscle fibres of the frog (Rana ridibunda). The repriming period, which was 11.2 ± 0.1 min (mean ± SEM, n = 9) on quiescent fibres, was shortened in fibres stimulated at a frequency ranging from 3 to 12 min−1 (optimal rate, 8 min−1; full repriming 5.7 ± 0.2 min; n = 10). A 10-fold increase in the extracellular calcium concentration shortened the repriming period on both stimulated and quiescent fibres, whereas decreasing external calcium (1/10) delayed it. In a Na+-free solution (Li+ substituted) the repriming period of stimulated fibres was markedly delayed (14 min), whereas quiescent fibres never recover more than 10% of their ability to develop subsequent caffeine contractures. In contrast, with a 35% Na solution, the repriming period was greatly shortened (stimulated, 5.4 ± 0.2 min, n = 7; quiescent, 6.2 ± 0.5 min, n = 8). It is concluded that repriming depends on three mechanisms that seem to refill a calcium store and trigger recovery: the slow inward calcium current, a Na+–Ca2+ exchange, and perhaps a passive Ca2 influx.
- 1 April 1987
- Published by Canadian Science Publishing in Canadian Journal of Physiology and Pharmacology
- Vol. 65 (4) , 704-710
Stimulation frequency and external ionic composition control the repriming of caffeine-induced contractures in frog skeletal muscle
The effect of stimulation rate and of external ionic composition on the repriming period of contractures induced by 6 mM caffeine was tested on isolated skeletal muscle fibres of the frog (Rana ridibunda). The repriming period, which was 11.2 ± 0.1 min (mean ± SEM, n = 9) on quiescent fibres, was shortened in fibres stimulated at a frequency ranging from 3 to 12 min−1 (optimal rate, 8 min−1; full repriming 5.7 ± 0.2 min; n = 10). A 10-fold increase in the extracellular calcium concentration shortened the repriming period on both stimulated and quiescent fibres, whereas decreasing external calcium (1/10) delayed it. In a Na+-free solution (Li+ substituted) the repriming period of stimulated fibres was markedly delayed (14 min), whereas quiescent fibres never recover more than 10% of their ability to develop subsequent caffeine contractures. In contrast, with a 35% Na solution, the repriming period was greatly shortened (stimulated, 5.4 ± 0.2 min, n = 7; quiescent, 6.2 ± 0.5 min, n = 8). It is concluded that repriming depends on three mechanisms that seem to refill a calcium store and trigger recovery: the slow inward calcium current, a Na+–Ca2+ exchange, and perhaps a passive Ca2 influx.