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For in vitro laboratory research use only/Not for human or veterinary use
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HMG 75iu

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HMG

75iu · Single vial · Lyophilized powder

Single vial44.99CAD

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Sender: Vennori Biosciences · orders@vennori.com

Dose
75iu
Pack size
Single vial
Form
Lyophilized powder
Storage
2–8°C

In vitro laboratory research use only · Not for human or veterinary use · Batch documented · Third-party tested · Ships from Canada

§ Research

Research · HMG

Overview

Human menopausal gonadotropin (hMG), also known as menotropins, is a gonadotropin preparation extracted and purified from the urine of postmenopausal women, in whom circulating gonadotropin concentrations are elevated. It contains both follicle-stimulating hormone (FSH) and luteinizing hormone (LH) bioactivity; in highly purified preparations, much of the LH activity is contributed by human chorionic gonadotropin. Both FSH and LH are heterodimeric glycoproteins sharing a common alpha subunit and distinguished by hormone-specific beta subunits. hMG is widely used as a comparator in gonadotropin pharmacology research, particularly in studies contrasting urinary-derived and recombinant gonadotropin preparations and their glycoform composition.

Mechanism of action

The FSH component binds the FSH receptor, a G-protein-coupled receptor on ovarian granulosa and testicular Sertoli cells, activating Gs-cAMP-protein kinase A signaling that drives follicular development and aromatase expression. The LH-activity component binds the luteinizing hormone/choriogonadotropin receptor on theca and Leydig cells, stimulating androgen synthesis. Under the two-cell, two-gonadotropin model, theca-derived androgens serve as substrate for granulosa-cell aromatization to estradiol, so the combined FSH and LH activity of hMG supports both steps of follicular steroidogenesis.

Key research findings

  1. 01

    Established as a urinary-derived reference preparation in comparative studies of FSH and LH receptor activity.

  2. 02

    Meta-analyses of randomized trials (2010) have compared highly purified hMG with recombinant FSH in assisted reproduction studies across follicular and oocyte-yield endpoints.

  3. 03

    A Cochrane systematic review (2011) characterized recombinant versus urinary gonadotropin preparations for ovarian stimulation, reporting comparable live-birth outcomes across products.

  4. 04

    Analytical studies document batch-level variation in the FSH-to-LH activity ratio, glycoform distribution, and hCG content of urinary preparations, which complicates direct comparison with recombinant products.

Published references

  • Clinical efficacy of highly purified hMG versus recombinant FSH in IVF/ICSI cycles: a meta-analysis

    Jee BC et al. — Gynecol Obstet Invest, 2010 · PMID: 20389096

  • Recombinant versus urinary gonadotrophin for ovarian stimulation in assisted reproductive technology cycles

    van Wely M et al. — Cochrane Database Syst Rev, 2011 · PMID: 21328276

The information above is derived from published preclinical and clinical research. It is provided for educational purposes only and does not constitute medical advice, diagnosis, or treatment recommendations.