experimental myopia, and ocular growth in chick. Invest Ophthalmol Vis Sci.

Abstract

PURPOSE. To learn whether ␥-aminobutyric acid (GABA) participates in retinal mechanisms that influence refractive development. METHODS. White leghorn chicks, some of which wore a unilateral goggle to induce myopia, received daily intravitreal injections of agonists or antagonists to the major GABA receptor subtypes. Eyes were studied with refractometry, ultrasound, and calipers. Retinas of other chicks wearing unilateral goggles were assayed for GABA content. RESULTS. Antagonists to GABA A or GABA A0r (formerly known as GABA C ) receptors inhibited form-deprivation myopia. GABA A antagonists showed greater inhibition of myopic growth in the equatorial than the axial dimension. A GABA A0r antagonist displayed parallel inhibition in the axial and equatorial dimensions. A GABA A0r agonist but not GABA A agonists altered the myopic refraction of goggled eyes. GABA B receptor antagonists, more so than an agonist, also slowed development of myopia, inhibiting axial growth more effectively than equatorial expansion of goggled eyes. When administered to nongoggled eyes, GABA A or GABA A0r agonists or antagonists also altered eye growth, chiefly stimulating it. Only a GABA A agonist induced a myopic refraction. Several of these agents stimulated eye growth in the axial, but not the equatorial, dimension. Retinal GABA content was slightly reduced in goggled eyes. CONCLUSIONS. GABA A , GABA A0r , and GABA B receptors modulate eye growth and refractive development. The anatomic effects of these drugs reinforce the notion that eye shape and not just eye size is regulated. A retinal site of action is consistent with the known ocular localizations of GABA and its receptors and with the altered retinal biochemistry in form-deprived eyes