In MT-GHRH transgenic mice, single iv doses of MZ-4-71 and MZ-5-156 decreased serum GH by 39-72% at 1 h.
In plain wordsIn mice with excess GHRH, one injection of either GHRH-blocking drug lowered blood growth hormone by 39 to 72% after one hour.
- Peptide
- Sermorelin
- Outcome
- DecreaseSerum GH after single iv antagonist dose
- Study
mousen: not reported in source
MT-GHRH transgenic mice overexpressing human GHRH- Outcome group
- Growth hormone and IGF-1 · Endocrine and hormones
Measurements
- Serum GH decrease
- 39 to 72%
- 1 h after iv antagonist
Source sentences
To ascertain whether MZ-4-71 and MZ-5-156 could antagonize the effect of hGHRH hyperstimulation in vivo, each antagonist was administered to MT-GHRH transgenic mice in a single iv dose of 10-200 microg. Both compounds decreased serum GH levels in transgenic mice by 39-72% at 1 h after injection.
1 context sentence(design, population, supporting numbers)
Transgenic mice overexpressing the human GH-releasing hormone (hGHRH) gene, an animal model of acromegaly, were used to investigate the effects of potent GHRH antagonists MZ-4-71 and MZ-5-156 on the excessive GH and insulin-like growth factor I (IGF-I) secretion caused by overproduction of hGHRH.
In this study, Sermorelin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Sermorelin.