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Published on: August 17, 2014
Swelling in the isolated perfused cornea induced by 12(R)hydroxyeicosatetraenoic acid
H F Edelhauser1, D H Geroski, W D Woods
1Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia.
Investigative Ophthalmology & Visual Science
|September 1, 1993
Summary
12(R)hydroxyeicosatetraenoic acid (12(R)HETE) causes corneal swelling by inhibiting endothelial pump function. This effect is linked to the inhibition of Na/K adenosine triphosphatase activity.
Area of Science:
- Ocular Surface Research
- Corneal Physiology
- Biochemistry
Background:
- Corneal edema is a significant clinical concern.
- Understanding the molecular mechanisms of corneal swelling is crucial for developing effective treatments.
- The role of specific eicosanoids in regulating corneal hydration is an active area of investigation.
Purpose of the Study:
- To investigate the impact of 12(R)hydroxyeicosatetraenoic acid (12(R)HETE) on corneal swelling.
- To determine the effect of 12(R)HETE on human and rabbit corneal endothelium.
- To elucidate the mechanism by which 12(R)HETE influences corneal hydration.
Main Methods:
- Excised human and rabbit corneas were utilized for in vitro experiments.
- Corneal endothelium was perfused with varying concentrations of 12(R)HETE.
- Comparisons were made between 12(R)HETE and its isomer 12(S)HETE, as well as with ouabain.
- Endothelial permeability and Na/K adenosine triphosphatase activity were assessed.
Main Results:
- 12(R)HETE induced a dose-dependent corneal swelling in a concentration-dependent manner.
- The swelling caused by 12(R)HETE was reversible upon removal of the compound.
- 12(R)HETE significantly inhibited Na/K adenosine triphosphatase activity, unlike 12(S)HETE.
- Endothelial permeability to carboxyfluorescein remained unaffected.
Conclusions:
- 12(R)HETE is identified as a causative agent of corneal swelling.
- The mechanism involves the inhibition of endothelial pump function.
- This inhibition is, at least partially, mediated by the suppression of Na/K adenosine triphosphatase activity.

