March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Estrogenic Effects on Rat Lacrimal Gland Function
Author Affiliations & Notes
  • Justin A. Saunders
    Ophthalmology, West Virginia Univ Eye Inst, Morgantown, West Virginia
  • Leon Rachel
    Neurosurgery, West Virginia Univ Department of Neurosurgery, Morgantown, West Virginia
  • Matheson Harris
    Ophthalmology, West Virginia Univ Eye Inst, Morgantown, West Virginia
  • Jason Huber
    Pharmacology, West Virginia Univ Department of Pharmacology, Morgantown, West Virginia
  • Charles Rosen
    Neurosurgery, West Virginia Univ Department of Neurosurgery, Morgantown, West Virginia
  • Jennifer Sivak
    Ophthalmology, West Virginia Univ Eye Inst, Morgantown, West Virginia
  • Footnotes
    Commercial Relationships  Justin A. Saunders, None; Leon Rachel, None; Matheson Harris, None; Jason Huber, None; Charles Rosen, None; Jennifer Sivak, None
  • Footnotes
    Support  Research to Prevent Blindness
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 621. doi:
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    • Get Citation

      Justin A. Saunders, Leon Rachel, Matheson Harris, Jason Huber, Charles Rosen, Jennifer Sivak; Estrogenic Effects on Rat Lacrimal Gland Function. Invest. Ophthalmol. Vis. Sci. 2012;53(14):621.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract
 
Purpose:
 

1. Determine estrogenic effects on tear production & breakup time. 2. Determine whether the rat lacrimal gland contains progesterone/estrogen sensitive receptors and the effect of estrogen..

 
Methods:
 

24 female Sprague-Dawlet rats, aged 15 months divided into two treatment arms. 1. 12 rats received subQ placebo pellet (Intact) 2. 12 rats received subQ pellet containing 1.5 mg of 17 beta-estradiol in a 90-day release matrix (E2) Both groups received treatment until 18 months of age. Serum estrogen level was measured prior to treatment and at 18 months of age using [I125] radioimmunoassay. Rats underwent induction with isoflurane anesthesia for 3 mins. Tear Volume Assessment: Modified Schirmer's filter paper strips placed in upper palpebral fissure for 5 mins. After 5 mins, test strips removed and tear height recorded. Tear Breakup Time: 1.0 microliter of fluorescein placed on the corneal surface followed by 3 manual blinks. Time to first break in tear film measured. Procedure was then repeated 3 times. Exenteration was performed on all 24 subjects. The orbital lacrimal gland was segmented and processed using H+E staining techniques as well as estrogen/progesterone sensitive histochemical processing.

 
Results:
 

1. Rats treated with placebo pellets had signficantly higher tear volume compared with estrogen-treated rats (one-way ANOVA with Tukey's post hoc analysis).2. Time to first breakup of tear film was significantly higher in rats treated with placebo pellets compared with those receiving estrogen (one-way ANOVA with Tukey's post hoc analysis).

 
Conclusions:
 

Estrogen supplementation leads to reduced tear volume and more rapid tear breakup time compared with age-matched controls.By using aged female rats treated with estrogen for 3 months, we created a model of keratoconjunctivitis sicca arising from hormone replacement therapy.  

 

 
Keywords: lacrimal gland • clinical laboratory testing • cornea: tears/tear film/dry eye 
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