The combination of letrozole and melatonin causes regression in size not histopathological scores on endometriosis in an experimental rat model
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Original Investigation
VOLUME: 10 ISSUE: 4
P: 199 - 204
December 2009

The combination of letrozole and melatonin causes regression in size not histopathological scores on endometriosis in an experimental rat model

J Turk Ger Gynecol Assoc 2009;10(4):199-204
1. Department Of Gynecology And Obstetrics Medical Faculty, Yeditepe University, Istanbul, Turkey
2. Center For Reproductive Medicine, Department Of Obstetrics And Gynecology, Yeditepe University Hospital, Istanbul, Turkey
3. Yeditepe University Hospital, Center For Reproductive Medicine, Head Of The Department Of Obstetrics, And Gynecology, Istanbul, Turkey
4. Yeditepe University Hospital, Department Of Obstetrics And Gynecology, Istanbul, Turkey
5. Yeditepe University Hospital, Department Of Pathology, Istanbul, Turkey
6. Yeditepe University Hospital, Department Of Physiology, Istanbul, Turkey
7. Department Of Physiology And Experimental Studies And Research Center, Yeditepe University School Of Medicine, Istanbul, Turkey
8. Department Of Obstetrics And Gynecology, Yeditepe University School Of Medicine, Istanbul, Turkey
No information available.
No information available
Received Date: 12.11.2009
Accepted Date: 30.11.2009
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ABSTRACT

Objective:

To determine the effects of the combination of letrozole and melatonin on surgically induced endometriosis.

Material and Methods:

This prospective, randomized, controlled, experimental study was carried out at Yeditepe University Experimental Research Center (YUDETAM). Female non-pregnant, 17 nulligravid Wistar - Hannover albino rats with surgically induced endometriosis were used in this study. Endometriosis was induced by using homologous uterine horn transplantation in the rats. Four operations were performed on each rat. The induction of endometriosis was performed in the first operation. After two weeks of estradiol treatment the second operation was performed and endometriotic lesions were evaluated. Estrogen was then discontinued and in the study groups medications were started. During two weeks the rats were given medications and the third operation was performed for the assessment of the effects of the medications on the endometriotic foci. Then all the medications were stopped and estrogen was started again. Two weeks later all the rats were euthanized and recurrence of endometriosis was evaluated.

Results:

The sum of the lesion volumes in the control group was 93.6±31.7 mm3 at the end of the second week. After the cessation of estradiol it decreased to 85.0±23.8 mm3 (P=0.31) and increased to 119.7±29.4 mm3 at the sixth week (P=0.02). A significant reduction in histopathologic scores were seen after cessation of the estradiol (p=0.04). At the end of the sixth week, histopathological scores reached the pretreatment values. In the letrozole and melatonin group the sum of the lesion volumes decreased significantly after the treatment (82.8±21.0 mm3 and 15.7±8.0 mm3 respectively). At the end of the sixth week, the mean volume was calculated as 43.9±31.8 mm3 (p=0.002). Histopathologic scores were 2.3±0.1, 2.0±0.2 and 2.2±0.3 at the end of the second, fourth and sixth weeks, respectively, in the letrozole and melatonin group.

Conclusions:

Letrozole and melatonin caused a significant regression in lesion volumes; however, histopathological scores of endometriotic lesions did not change significantly.

Keywords:
Endometriosis, melatonin, letrozole, rat endometriosis