Signalling Pathways Activated by 5-HT1B/5-HT1D Receptors in Native Smooth Muscle and Primary Cultures of Rabbit Renal Artery Smooth Muscle Cells

2000 ◽  
Vol 37 (6) ◽  
pp. 457-468 ◽  
Author(s):  
J.M. Hinton ◽  
P.B. Hill ◽  
J.Y. Jeremy ◽  
C.J. Garland
1998 ◽  
Vol 63 (4) ◽  
pp. 225-236 ◽  
Author(s):  
Pascale Etienne ◽  
Núria Parés-Herbuté ◽  
Louis Monnier ◽  
Herisoa Rabesandratana ◽  
Laurence Mani-Ponset ◽  
...  

2007 ◽  
Vol 582 (1) ◽  
pp. 41-61 ◽  
Author(s):  
Takashi Sakamoto ◽  
Toshihiro Unno ◽  
Takio Kitazawa ◽  
Tetsuro Taneike ◽  
Masahisa Yamada ◽  
...  

Aging Cell ◽  
2018 ◽  
pp. e12844 ◽  
Author(s):  
Bethan A. Brown ◽  
Georgia M. Connolly ◽  
Carina E. J. Mill ◽  
Helen Williams ◽  
Gianni D. Angelini ◽  
...  

2002 ◽  
Vol 34 (6) ◽  
pp. A68
Author(s):  
Sabina Vogel ◽  
Thomas Kubin ◽  
Elisabeth Deindl ◽  
Matthias Heil ◽  
Wolfgang Schaper ◽  
...  

1989 ◽  
Vol 256 (3) ◽  
pp. C644-C651 ◽  
Author(s):  
M. G. Blennerhassett ◽  
M. S. Kannan ◽  
R. E. Garfield

The membrane potential (Em) of cultured aortic smooth muscle cells from Sprague-Dawley (SD), Wistar-Kyoto (WKY), and spontaneously hypertensive (SHR) rats was measured in proliferating primary cultures. Em of SD cells in high-density cultures was -51 to -58 mV, whereas that of low-density cultures (1-2 days) was -30 mV. This difference was due to a continuous process of hyperpolarization during proliferation in culture. Em of WKY and SHR hyperpolarized similarly, from -12 to -42 and -38 mV, respectively. Hyperpolarization of Em of SD, WKY, and SHR cells was related to cell density rather than time in culture. Em may be a sensitive and significant indicator of the changes in the differentiated state expressed by proliferating smooth muscle in vitro.


1986 ◽  
Vol 32 (2) ◽  
pp. 173-180 ◽  
Author(s):  
Maria Sjölund ◽  
Kjell Madsen ◽  
Klaus von der Mark ◽  
Johan Thyberg

1988 ◽  
Vol 46 ◽  
pp. 185
Author(s):  
Masayasu Kimura ◽  
Shinjiro Kobayashi ◽  
Kouhei Notoya ◽  
Yasuhiko Mimura ◽  
Jun Suzuki ◽  
...  

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