Multiple effects of adenosine in the arterially perfused mammalian eye. Possible mechanisms for the neuroprotective function of adenosine in the retina - Adenosine in the perfused eye

被引:13
作者
Macaluso, C [1 ]
Frishman, LJ
Frueh, B
Kaelin-Lang, A
Onoe, S
Niemeyer, G
机构
[1] Univ Parma, Dept Ophthalmol, I-43100 Parma, Italy
[2] Univ Houston, Coll Optometry, Houston, TX USA
[3] Univ Bern, Dept Ophthalmol, Bern, Switzerland
[4] Univ Bern, Dept Neurol, Bern, Switzerland
[5] Dept Ophthalmol, Himeji, Hyogo, Japan
[6] Univ Zurich, Dept Ophthalmol, Physiol Lab, Zurich, Switzerland
关键词
adenosine; isolated perfused cat eye; neuroprotection; optic nerve; retina; retinal ganglion cells;
D O I
10.1023/A:1022456615715
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
It has been postulated that the major physiological role of adenosine is protection of the central nervous system in conditions such as ischemia, hypoxia, or prolonged neuronal excitation. Under these conditions adenosine is released, and exerts multiple effects, including vasodilation, inhibition of neuronal activity, and enhancement of glycogenolysis, resulting in neuroprotection. In this article, published as well as unpublished data on the multiple effects of exogenous adenosine and application of adenosine-related agents, performed using the arterially perfused cat eye, will be reviewed and discussed within the framework of the neuroprotective role of adenosine. The isolated, arterially perfused eye preparation has the advantage of combining integrity of the eye structure, exact control of arterial concentration and timing of applied pharmacological agents, and access to electrophysiological parameters of both retina and optic nerve, as well as the ability to control and monitor perfusate flow. The absence of red blood cells in the perfusate prevents adenosine from being metabolized prior to reaching the eye.
引用
收藏
页码:51 / 59
页数:9
相关论文
共 58 条
[1]   RELEASE OF ADENOSINE FROM ISCHEMIC BRAIN - EFFECT ON CEREBRAL VASCULAR-RESISTANCE AND INCORPORATION INTO CEREBRAL ADENINE-NUCLEOTIDES [J].
BERNE, RM ;
RUBIO, R ;
CURNISH, RR .
CIRCULATION RESEARCH, 1974, 35 (02) :262-271
[2]  
BLAZYNSKI C, 1989, INVEST OPHTH VIS SCI, V30, P2533
[3]   DISCRETE-DISTRIBUTIONS OF ADENOSINE RECEPTORS IN MAMMALIAN RETINA [J].
BLAZYNSKI, C .
JOURNAL OF NEUROCHEMISTRY, 1990, 54 (02) :648-655
[4]   ADENOSINE IN VERTEBRATE RETINA - LOCALIZATION, RECEPTOR CHARACTERIZATION, AND FUNCTION [J].
BLAZYNSKI, C ;
PEREZ, MTR .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 1991, 11 (05) :463-484
[5]   HIGH-AFFINITY CAMP-PHOSPHODIESTERASE AND ADENOSINE LOCALIZED IN SENSORY ORGANS [J].
BORISY, FF ;
HWANG, PN ;
RONNETT, GV ;
SNYDER, SH .
BRAIN RESEARCH, 1993, 610 (02) :199-207
[6]   ENDOGENOUS ADENOSINE AND ADENOSINE RECEPTORS LOCALIZED TO GANGLION-CELLS OF THE RETINA [J].
BRAAS, KM ;
ZARBIN, MA ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (11) :3906-3910
[7]   THE POTENTIAL ROLE OF ADENOSINE IN REGULATING BLOOD-FLOW IN THE EYE [J].
BRAUNAGEL, SC ;
XIAO, JG ;
CHIOU, GCY .
JOURNAL OF OCULAR PHARMACOLOGY, 1988, 4 (01) :61-73
[8]   ADENOSINE AND ITS AGONISTS CAUSE RETINAL VASODILATION AND HEMORRHAGES - IMPLICATIONS FOR ISCHEMIC RETINOPATHIES [J].
CAMPOCHIARO, PA ;
SEN, HA .
ARCHIVES OF OPHTHALMOLOGY, 1989, 107 (03) :412-416
[9]   A2A adenosine receptor deficiency attenuates brain injury induced by transient focal ischemia in mice [J].
Chen, JF ;
Huang, ZH ;
Ma, JY ;
Zhu, JM ;
Moratalla, R ;
Standaert, D ;
Moskowitz, MA ;
Fink, JS ;
Schwarzschild, MA .
JOURNAL OF NEUROSCIENCE, 1999, 19 (21) :9192-9200
[10]   ADENOSINE, AN ENDOGENOUS ANTIINFLAMMATORY AGENT [J].
CRONSTEIN, BN .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 76 (01) :5-13