Manipulation of intraocular pressure for studying the effects on accommodation.

A reliable experimental system in which IOP can be manipulated or a rapid IOP change can be induced while simultaneously and continuously measuring IOP and the ocular accommodative changes would be useful for understanding the physiological effect of intraocular pressure (IOP) on the accommodative mechanism. In this study, an IOP perfusion and recording system was developed and tested using 13 enucleated pig eyes. The vitreous chamber of the pig eyes was cannulated with a needle connected to two fluid reservoirs at different heights. One reservoir was set to achieve one of three baseline pressures of 5.5 mmHg, 13.0 mmHg and 20.5 mmHg. The other reservoir was moved to achieve pressures of 1.5 mmHg, 3.0 mmHg, 4.5 mmHg and 6.0 mmHg higher than the baseline pressure. The height differential between the reservoirs determined the amplitude of IOP changes. Rapid IOP changes were induced by switching the reservoirs with a solenoid pinch-valve. Two needles, one each attached to a pressure transducer were inserted into the anterior chamber and vitreous chamber respectively. Custom developed software was used to measure the anterior chamber pressure and vitreous chamber pressure at 80 Hz. A high-resolution continuous A-scan ultrasound biometer (CUB) was used to dynamically measure changes in ocular biometry including anterior chamber depth (ACD), lens thickness (LT) and vitreous chamber depth (VCD) while the vitreous chamber pressure was manipulated. The changes in ACD, LT and VCD were analyzed as a function of the pressure change. Perfusion-induced axial biometric changes were quantified by the slopes of linear regression relationships. Both anterior chamber pressure and vitreous chamber pressure changed relatively systematically with the induced vitreous chamber pressure changes (anterior chamber: y = 0.863x + 0.030, r(2) = 0.983; vitreous chamber: y = 0.883x + 0.009, r(2) = 0.981). At perfusion pressures of 5.5, 13.0 and 20.5 mmHg, the slopes for ACD were -5.72, -2.75 and -2.36 μm/mmHg, for LT were -3.31, -1.59 and -1.03 μm/mmHg and for VCD were 19.05, 8.63 and 5.18 μm/mmHg. The system was able to manipulate and monitor IOP while axial biometry changes were recorded. This system will allow the relationship between IOP and accommodation to be studied in non-human primate eyes.