Fluid circulation determined in the isolated bovine lens

Invest Ophthalmol Vis Sci. 2012 Oct 11;53(11):7087-96. doi: 10.1167/iovs.12-10295.

Abstract

Purpose: In 1997, a theoretical model was developed that predicted the existence of an internal, Na(+)-driven fluid circulation from the poles to the equator of the lens. In the present work, we demonstrate with a novel system that fluid movement can be measured across the polar and equatorial surface areas of isolated cow lenses. We have also determined the effects of ouabain and reduced bath [Na(+)].

Methods: Lenses were isolated in a chamber with three compartments separated by two thin O-rings. Each compartment, anterior (A), equatorial (E), and posterior (P), was connected to a vertical capillary graduated in 0.25 μL. Capillary levels were read every 15 minutes. The protocols consisted of 2 hours in either open circuit or short circuit. The effects of ouabain and low-Na(+) solutions were determined under open circuit.

Results: In 21 experiments, the E capillary increased at a mean rate of 0.060 μL/min while the A and P levels decreased at rates of 0.044 and 0.037 μL/min, respectively, closely accounting for the increase in E. The first-hour flows under short circuit were approximately 40% larger than those in open-circuit conditions. The first-hour flows were always larger than those during the second hour. Preincubation of lenses with either ouabain or low-[Na(+)] solutions resulted in reduced rates of fluid transport. When KCl was used to replace NaCl, a transitory stimulation of fluid transport occurred.

Conclusions: These experiments support that a fluid circulation consistent with the 1997 model is physiologically active.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Fluids / metabolism*
  • Capillaries / physiology
  • Capillary Permeability / drug effects
  • Cattle
  • Diffusion Chambers, Culture
  • Electronics / methods
  • Enzyme Inhibitors / pharmacology
  • Equipment Design
  • Hydrostatic Pressure
  • In Vitro Techniques
  • Lens, Crystalline / physiology*
  • Models, Biological
  • Ouabain / pharmacology
  • Potassium / pharmacokinetics
  • Sodium / pharmacokinetics
  • Sodium Chloride / pharmacokinetics
  • Water-Electrolyte Balance / drug effects
  • Water-Electrolyte Balance / physiology*

Substances

  • Enzyme Inhibitors
  • Sodium Chloride
  • Ouabain
  • Sodium
  • Potassium