hCG
| Category | Compounds |
|---|---|
| Also known as | Human Chorionic Gonadotropin, Choriogonadotropin |
| Last updated | 2026-04-14 |
| Reading time | 3 min read |
| Tags | reproductiveendocrinegonadotropinfertilityresearch |
Overview
Human chorionic gonadotropin (hCG) is a placental glycoprotein hormone best known for its role in early pregnancy, where it supports the corpus luteum and progesterone production. hCG is structurally and functionally similar to luteinizing hormone (LH) and activates the same receptor. This LH-like activity makes hCG a valuable tool in reproductive endocrinology research, fertility treatment, and hypogonadism studies.
Clinically, hCG is used to trigger ovulation in assisted reproduction protocols, to stimulate testicular testosterone production in men with secondary hypogonadism, and in certain pediatric endocrine conditions such as undescended testes. Recombinant forms (choriogonadotropin alfa) are available alongside urinary-derived preparations from pooled pregnancy urine.
hCG is frequently discussed in peptide research contexts alongside GnRH analogs including Gonadorelin, Buserelin, Triptorelin, and Leuprolide, because all these compounds operate within the hypothalamic-pituitary-gonadal axis that hCG influences downstream.
Structure / Chemistry
hCG is a heterodimeric glycoprotein with α and β subunits. Its α subunit is shared with LH, FSH, and TSH. The β subunit is largely unique to hCG and is the basis of specific immunoassays. Extensive glycosylation — including N- and O-linked glycans — contributes to its long half-life relative to LH.
Mechanism of Action
hCG binds LH/CG receptors on ovarian theca cells, granulosa cells, and testicular Leydig cells. Activation stimulates cAMP production and steroidogenesis, leading to testosterone production in men and progesterone/estradiol production in women. The LH-like action enables hCG to "mimic" an LH surge for ovulation induction and to sustain testicular steroidogenesis when endogenous LH is suppressed.
Research Summary
| Area | Finding | Reference |
|---|---|---|
| Ovulation induction | hCG triggers ovulation after FSH stimulation | Multiple ART trials |
| Hypogonadism | Maintains spermatogenesis with testosterone-replacement alternatives | Coviello et al., J Clin Endocrinol Metab 2005 |
| Pregnancy | Supports corpus luteum progesterone | Classical reproductive endocrinology |
| Cryptorchidism | Historical pediatric use for testicular descent | Pediatric endocrinology literature |
| Assay | β-subunit used for pregnancy testing | Standard diagnostic practice |
Pharmacokinetics
hCG has a long half-life for a glycoprotein hormone — approximately 24-36 hours for the initial phase after intramuscular or subcutaneous injection. Clinical protocols use dosing schedules ranging from a single ovulation-trigger injection to intermittent smaller injections for chronic testicular support. Specific doses are clinical parameters, not guidance.
Common Discussion Topics
- Distinction from testosterone replacement in male hypogonadism research.
- Preservation of testicular volume and spermatogenesis.
- Use in IVF and ART protocols.
- Relationship to LH and cross-reactivity with its receptor.
- Unapproved off-label weight-loss claims and associated regulatory concerns.
Related Compounds
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Related entries
- Buserelin—
- GnRH (Gonadotropin-Releasing Hormone)— A hypothalamic decapeptide that serves as the master regulator of the hypothalamic-pituitary-gonadal axis, controlling reproduction through pulsatile release patterns, with numerous synthetic analogs used clinically for fertility, cancer, and endocrine disorders.
- Gonadorelin— A synthetic form of the naturally occurring gonadotropin-releasing hormone (GnRH), a hypothalamic decapeptide that stimulates pituitary release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), used clinically in fertility treatment and diagnostics.
- Leuprolide— A synthetic GnRH agonist that, through sustained administration, suppresses gonadotropin release and downstream sex hormone production, used in prostate cancer, endometriosis, precocious puberty, and other hormone-dependent conditions.
- Triptorelin— A synthetic decapeptide GnRH agonist used for prostate cancer, central precocious puberty, and endometriosis, achieving sex hormone suppression through pituitary GnRH receptor downregulation after initial stimulatory phase.