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Published on: April 19, 2017
The Adenosine Receptor Antagonist, 7-Methylxanthine, Alters Emmetropizing Responses in Infant Macaques
Li-Fang Hung1,2, Baskar Arumugam1,2, Lisa Ostrin1
1College of Optometry, University of Houston, Houston, Texas, United States.
Purpose:
Previous studies suggest that the adenosine receptor antagonist, 7-methylxanthine (7-MX), retards myopia progression. Our aim was to determine whether 7-MX alters the compensating refractive changes produced by defocus in rhesus monkeys.
Methods:
Starting at age 3 weeks, monkeys were reared with -3 diopter (D; n = 10; 7-MX -3D/pl) or +3D (n = 6; 7-MX +3D/pl) spectacles over their treated eyes and zero-powered lenses over their fellow eyes. In addition, they were given 100 mg/kg of 7-MX orally twice daily throughout the lens-rearing period (age 147 ± 4 days). Comparison data were obtained from lens-reared controls (-3D/pl, n = 17; +3D/pl, n = 9) and normal monkeys (n = 37) maintained on a standard diet. Refractive status, corneal power, and axial dimensions were assessed biweekly.
Results:
The -3D/pl and +3D/pl lens-reared controls developed compensating myopic (-2.10 ± 1.07 D) and hyperopic anisometropias (+1.86 ± 0.54 D), respectively. While the 7-MX +3D/pl monkeys developed hyperopic anisometropias (+1.79 ± 1.11 D) that were similar to those observed in +3D/pl controls, the 7-MX -3D/pl animals did not consistently exhibit compensating myopia in their treated eyes and were on average isometropic (+0.35 ± 1.96 D). The median refractive errors for both eyes of the 7-MX -3D/pl (+5.47 D and +4.38 D) and 7-MX +3D/pl (+5.28 and +3.84 D) monkeys were significantly more hyperopic than that for normal monkeys (+2.47 D). These 7-MX-induced hyperopic ametropias were associated with shorter vitreous chambers and thicker choroids.
Conclusions:
In primates, 7-MX reduced the axial myopia produced by hyperopic defocus, augmented hyperopic shifts in response to myopic defocus, and induced hyperopia in control eyes. The results suggest that 7-MX has therapeutic potential in efforts to slow myopia progression.
Insights
7-methylxanthine (7-MX) altered refractive development in rhesus monkeys. This adenosine receptor antagonist reduced myopia progression and induced hyperopia, suggesting therapeutic potential for myopia control.
Area of Science:
- Ophthalmology
- Pharmacology
- Primate Research
Background:
- Myopia progression is a significant concern.
- Adenosine receptor antagonists, like 7-methylxanthine (7-MX), have shown potential in slowing myopia.
- The effect of 7-MX on compensatory refractive changes is not well understood.
Purpose of the Study:
- To investigate whether 7-methylxanthine (7-MX) alters compensatory refractive changes induced by defocus in rhesus monkeys.
- To evaluate the therapeutic potential of 7-MX in myopia control.
Main Methods:
- Rhesus monkeys were reared with -3D or +3D spectacles from 3 weeks of age.
- Monkeys received oral 7-MX (100 mg/kg twice daily) throughout the lens-rearing period.
- Refractive status, corneal power, and axial dimensions were assessed biweekly.
Main Results:
- Monkeys treated with 7-MX and -3D lenses did not develop expected myopia and became isometropic.
- Monkeys treated with 7-MX and +3D lenses showed hyperopic anisometropias similar to controls.
- Both 7-MX groups exhibited significant hyperopia compared to normal monkeys, associated with shorter vitreous chambers and thicker choroids.
Conclusions:
- In primates, 7-MX reduced myopia induced by hyperopic defocus and increased hyperopic shifts with myopic defocus.
- 7-MX also induced hyperopia in control eyes, suggesting a broader impact on refractive development.
- These findings support the therapeutic potential of 7-MX for slowing myopia progression.
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