Estrogens exert route- and dose-dependent effects on insulin-like growth factor (IGF)-binding protein-3 and the acid-labile subunit of the IGF ternary complex.

Article Details

Citation

Kam GY, Leung KC, Baxter RC, Ho KK

Estrogens exert route- and dose-dependent effects on insulin-like growth factor (IGF)-binding protein-3 and the acid-labile subunit of the IGF ternary complex.

J Clin Endocrinol Metab. 2000 May;85(5):1918-22.

PubMed ID
10843175 [ View in PubMed
]
Abstract

We have previously shown that exogenous estrogens exert route-dependent effects on serum GH and insulin-like growth factor I (IGF-I) levels. IGF-I circulates as a ternary complex with IGF-binding protein-3 (IGFBP-3) and the acid-labile subunit (ALS). It is not known whether IGFBP-3 and ALS in blood are regulated by estrogen and, if so, whether this is also route dependent. In the present study we investigate the effects on IGFBP-3 and ALS of oral and transdermal estrogens (study 1), of different oral estrogen formulations (ethinyl estradiol, conjugated estrogen, and estradiol valerate; study 2), of different estrogen dosages (study 3) in normal postmenopausal women, and of oral estrogen in hypogonadal GH-deficient women (study 4). Administration of oral, but not transdermal, estrogen in normal postmenopausal women significantly decreased serum levels of IGFBP-3 and ALS (P < or = 0.005). The suppressive effects were similar with different oral estrogen formulations, and the degree of suppression increased with estrogen dosage. In hypogonadal GH-deficient women, oral estrogen treatment also significantly reduced IGFBP-3 and ALS (P = 0.02). The changes in IGF-I in each of the four studies paralleled the changes in both IGFBP-3 and ALS. In conclusion, exogenous estrogens suppress serum IGFBP-3 and ALS in a route- and dose-dependent manner, which are in parallel with the effects on serum IGF-I. These actions of oral estrogen are independent of endogenous GH status.

DrugBank Data that Cites this Article

Pharmaco-proteomics
DrugDrug GroupsGeneGene IDChangeInteractionChromosome
EstradiolApproved Investigational Vet ApprovedFSHB2488
decreased
estradiol valerate results in decreased expression of FSHB protein11p14.1
EstradiolApproved Investigational Vet ApprovedIGF13479
decreased
estradiol valerate results in decreased expression of IGF1 protein12q23.2
EstradiolApproved Investigational Vet ApprovedIGFALS3483
decreased
estradiol valerate results in decreased expression of IGFALS protein16p13.3
EstradiolApproved Investigational Vet ApprovedIGFBP33486
decreased
estradiol valerate results in decreased expression of IGFBP3 protein7p12.3
EstradiolApproved Investigational Vet ApprovedLHB3972
decreased
estradiol valerate results in decreased expression of LHB protein19q13.3
EthinylestradiolApprovedIGFALS3483
decreased
Ethinyl Estradiol results in decreased expression of IGFALS protein16p13.3
EthinylestradiolApprovedIGFBP33486
decreased
Ethinyl Estradiol results in decreased expression of IGFBP3 protein7p12.3
EstradiolApproved Investigational Vet ApprovedGH12688
increased
estradiol valerate results in increased expression of GH1 protein17q23.3
EthinylestradiolApprovedGH12688
increased
Ethinyl Estradiol results in increased expression of GH1 protein17q23.3
EthinylestradiolApprovedLHB3972
decreased
Ethinyl Estradiol results in decreased expression of LHB protein19q13.3
EthinylestradiolApprovedLHB3972
decreased
Ethinyl Estradiol results in decreased expression of LHB protein19q13.3
EthinylestradiolApprovedFSHB2488
decreased
Ethinyl Estradiol results in decreased expression of FSHB protein11p14.1
EthinylestradiolApprovedFSHB2488
decreased
Ethinyl Estradiol results in decreased expression of FSHB protein11p14.1
EthinylestradiolApprovedFSHB2488
decreased
Ethinyl Estradiol results in decreased expression of FSHB protein11p14.1
EthinylestradiolApprovedIGF13479
decreased
Ethinyl Estradiol results in decreased expression of IGF1 protein12q23.2
EthinylestradiolApprovedIGF13479
decreased
Ethinyl Estradiol results in decreased expression of IGF1 protein12q23.2