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Stimulation of Ovulation in Immature Female Rats Using Orthosteric and Allosteric Luteinizing Hormone Receptor
E A Fokina1, K V Derkach1, A A Bakhtyukov1
1Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia.
A novel compound, TP03, shows promise as an ovulation inducer and ovarian steroidogenesis stimulator. It acts similarly to human chorionic gonadotropin (hCG) but without causing ovarian hyperstimulation syndrome.
Area of Science:
- Reproductive Endocrinology
- Pharmacology
Background:
- Human chorionic gonadotropin (hCG) and luteinizing hormone (LH) are standard treatments for reproductive disorders and ovulation induction.
- Their clinical use is restricted by potential side effects.
Purpose of the Study:
- To evaluate TP03, an allosteric agonist of the LH/hCG receptor, as a potential alternative to hCG and LH.
- To assess TP03's efficacy in inducing ovulation and stimulating ovarian steroidogenesis.
Main Methods:
- Immature female rats were pretreated with Follimag.
- TP03 (50 mg/rat, i.p.) was administered.
- Progesterone levels and corpus luteum formation were assessed post-treatment.
- Vascular endothelial growth factor (VEGF) expression was analyzed.
Main Results:
- TP03 administration increased progesterone levels within 8 hours and induced ovulation, evidenced by corpus luteum formation (8.6 ± 0.5 per ovary at 24 h).
- TP03 demonstrated comparable activity to hCG but with a more moderate effect.
- Unlike hCG, TP03 did not elevate VEGF expression, mitigating the risk of ovarian hyperstimulation syndrome.
Conclusions:
- TP03 is a potent ovulation inducer and ovarian steroidogenesis stimulator.
- Its mechanism of action offers a potentially safer alternative to hCG, avoiding VEGF-related side effects.
- TP03 represents a promising therapeutic candidate for reproductive treatments.
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