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PMID: 10511627 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Effect of A1 adenosine receptor agonist upon cochlear dysfunction induced by transient ischemia.

Hearing research ·Vol. 136 ·No. 1-2 ·1999-10-00 ·Pages 86-90

Tabuchi K, Ito Z, Wada T, Takahashi K, Hara A, Kusakari J

Abstract

The present study was undertaken to determine whether 2-chloro-N6-cyclopentyladenosine (CCPA), a highly selective A1 adenosine receptor agonist, attenuated cochlear dysfunction induced by transient ischemia or not. Ischemia of different durations (15, 30 or 60 min) was induced in 46 albino guinea pigs by transiently pressing the labyrinthine artery. CCPA or physiological saline solution was intraperitoneally administered to the animals 15 min prior to ischemia. The post-ischemic CAP threshold shift from the pre-administration value was measured 4 h after the onset of reperfusion to assess post-ischemic cochlear dysfunction. A statistically significant reduction in the CAP threshold shift was seen in CCPA-given animals after 15- and 30-min ischemia, whereas there was no statistical difference after 60-min ischemia. These results suggest that A1 adenosine receptor agonist exerts a protective effect on the cochlear injury induced by transient ischemia of intermediate duration.

MeSH Terms
Action Potentials/drug effects Adenosine/analogs & derivatives,pharmacology Animals Cochlea/blood supply,drug effects,physiopathology Differential Threshold/drug effects Guinea Pigs Ischemia/physiopathology Purinergic P1 Receptor Agonists
Chemicals
Purinergic P1 Receptor Agonists 2-chloro-N(6)cyclopentyladenosine Adenosine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Tabuchi K
Department of Otolaryngology, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Japan.
Ito Z
Wada T
Takahashi K
Hara A
Kusakari J
Article Info
Journal
Hearing research
Abbr.
Hear Res
ISSN
0378-5955
Published
1999-10-00
Pages
86-90
Language
English
Region
Netherlands
NLM ID
7900445
Subset
IM
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