Changes in acetylcholine release from the chick retina are not associated with myopia development
Creators
- 1. The University of Melbourne, VIC (Australia). Department of Optometry and Vision Sciences
Description
Full text: The effectiveness of muscarinic receptor antagonists in inhibiting myopia progression in animal models and humans implicates cholinergic signalling in ocular growth regulation. Therefore to determine if changes in the release of acetylcholine from the retina are involved in myopia development, the efflux of acetylcholine from the in vitro retina of normal and myopic chick eyes was investigated. Chicks were monocularly deprived (MD) of pattern vision with translucent occluders for 2 or 7 days and refractive error of MD groups and age matched normals was monitored using retinoscopy (n=6 each group). 3H-choline-Cl (1 Ci in 7μL) was injected into the vitreous of each eye under 2.5% halothane anaesthesia. After 1hr, the eyes were enucleated, under terminal anaesthesia (sodium pentobarbital, 120 mg/kg, im). Retinas were flat-mounted on acetate filter discs and superfused with oxygenated physiological saline solution (PSS) for 30min at 0.4mL/min. Five baseline fractions were collected (B1-B5), then three stimulated fractions were collected in the presence of PSS containing 50mM KCl (K1-K3) at 2min intervals. 3H-acetylcholine ( 3H-ACh) in each fraction was quantified by liquid scintillation counting. Significant amounts of myopia were induced in MD eyes after 2 (-5.1±0.8D) and 7 days (-18.8±2.4D) relative to control eyes (paired t-test p<0.01). KCl evoked 3H-ACh release was 146±15% above basal levels (K2/B1%) from retinas of normal animals. After 2 days MD, there was no significant difference between KCl-evoked release of 3H-ACh from deprived eyes (147 39%) compared to control eyes (198±61%, paired t-test, p=0.27) or the eyes of normal animals (ANOVA, p>0.5). Similar results were obtained following 7 days MD. The results demonstrate that evoked acetylcholine release from the chick retina of myopic eyes is unaltered relative to control or normal eyes using an in vitro approach. Copyright (2002) Australian Neuroscience Society
Availability note (English)
Available in abstract form only, full text entered in this recordAdditional details
Publishing Information
- Journal Title
- Proceedings of the Australian Neuroscience Society
- Journal Volume
- 13
- Journal Page Range
- p. 301
- ISSN
- 1034-3237
Conference
- Title
- 22. Annual Meeting of the Australian Neuroscience Society
- Dates
- 4-6 Feb 2002
- Place
- Sydney, NSW (Australia)
INIS
- Country of Publication
- Australia
- Country of Input or Organization
- Australia
- INIS RN
- 34078422
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- BIOLOGICAL MODELS; CHICKENS; CHOLINE; DATA ANALYSIS; GROWTH; IN VITRO; LABELLED COMPOUNDS; RETINA; SCINTISCANNING; SENSE ORGANS DISEASES; STATISTICS; TIME DEPENDENCE; TRITIUM
- Descriptors DEC
- ALCOHOLS; AMINES; AMMONIUM COMPOUNDS; ANIMALS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BIRDS; BODY; COUNTING TECHNIQUES; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EYES; FACE; FOWL; HEAD; HYDROGEN ISOTOPES; HYDROXY COMPOUNDS; ISOTOPES; LIGHT NUCLEI; LIPOTROPIC FACTORS; MATHEMATICS; NUCLEI; ODD-EVEN NUCLEI; ORGANIC COMPOUNDS; ORGANS; QUATERNARY COMPOUNDS; RADIOISOTOPE SCANNING; RADIOISOTOPES; SENSE ORGANS; VERTEBRATES; YEARS LIVING RADIOISOTOPES