mRNA levels measured by qRT-PCR from the uterus and endometriosis vesicles.

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AI-generated summary by claude@2026-07, 2026-07-15

This study measured mRNA levels of CRHR1, CRHR2, and GR in uterine tissue and endometriosis vesicles of rats, comparing results to sham-operated controls.

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AI-generated deep summary by claude@2026-07, 2026-07-15 · read from full text

The study examined whether antagonizing corticotropin-releasing hormone receptor 1 (CRHR1) with the antagonist antalarmin alters uterine and lesion-related gene expression in an endometriosis rat model. Using qRT-PCR, the authors measured mRNA levels of CRHR1, CRHR2, and the glucocorticoid receptor (GR), normalizing expression to the uterus of sham rats, with n=9 per vehicle and antalarmin group. They reported significant differences (p<0.05) indicated by comparing antalarmin-treated tissue to sham uterus, although the figure text does not specify directionality for each gene. This paper is centrally about endometriosis — it focuses on reducing endometriosis progression via CRHR1 antagonism and includes qRT-PCR of uterine and endometriosis vesicle gene expression.

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Abstract

(A) corticotropin releasing hormone receptor type 1 (CRHR1). (B) corticotropin releasing hormone receptor type 2 (CRHR2). (C) Glucocorticoid receptor (GR). Data normalized to the uterus of sham rats. * represents p< 0.05 compared to sham rats’ uterus. For all panels, n = 9 in vehicle and antalarmin groups.
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Antagonizing the corticotropin releasing hormone receptor 1 with antalarmin reduces the progression of endometriosis Fig 9 mRNA levels measured by qRT-PCR from the uterus and endometriosis vesicles. (A) corticotropin releasing hormone receptor type 1 (CRHR1). (B) corticotropin releasing hormone receptor type 2 (CRHR2). (C) Glucocorticoid receptor (GR). Data normalized to the uterus of sham rats. * represents p< 0.05 compared to sham rats’ uterus. For all panels, n = 9 in vehicle and antalarmin groups.

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endometriosis

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last seen: 2026-05-13T20:12:55.465734+00:00
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