Papers

Peer-reviewed
Jan, 2015

PDE4 and PDE5 regulate cyclic nucleotide contents and relaxing effects on carbachol-induced contraction in the bovine abomasum

JOURNAL OF VETERINARY MEDICAL SCIENCE
  • Takeharu Kaneda
  • ,
  • Yuuki Kido
  • ,
  • Tsuyoshi Tajima
  • ,
  • Norimoto Urakawa
  • ,
  • Kazumasa Shimizu

Volume
77
Number
1
First page
15
Last page
19
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1292/jvms.14-0248
Publisher
JAPAN SOC VET SCI

The effects of various selective phosphodiesterase (PDE) inhibitors on carbachol (CCh)-induced contraction in the bovine abomasum were investigated. Various selective PDE inhibitors, vinpocetine (type 1), erythro-9-(2-hydroxy-3-nonyl) adenine (EHNA, type 2), milrinone (type 3), Ro20-1724 (type 4), vardenafil (type 5), BRL-50481 (type 7) and BAY73-6691 (type 9), inhibited CCh-induced contractions in a concentration-dependent manner. Among the PDE inhibitors, Ro20-1724 and vardenafil induced more relaxation than the other inhibitors based on the data for the IC50 or maximum relaxation. In smooth muscle of the bovine abomasum, we showed the expression of PDE4B, 4C, 4D and 5 by RT-PCR analysis. In the presence of CCh, Ro20-1724 increased the cAMP content, but not the cGMP content. By contrast, vardenafil increased the cGMP content, but not the cAMP content. These results suggest that Ro20-1724-induced relaxation was correlated with cAMP and that vardenafil-induced relaxation was correlated with cGMP in the bovine abomasum. In conclusion, PDE4 and PDE5 are the enzymes involved in regulation of the relaxation associated with cAMP and cGMP, respectively, in the bovine abomasum.

Link information
DOI
https://doi.org/10.1292/jvms.14-0248
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/25319411
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349533
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000349275400003&DestApp=WOS_CPL
ID information
  • DOI : 10.1292/jvms.14-0248
  • ISSN : 0916-7250
  • eISSN : 1347-7439
  • Pubmed ID : 25319411
  • Pubmed Central ID : PMC4349533
  • Web of Science ID : WOS:000349275400003

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