In GH1 rat tumor cells, hexarelin significantly stimulated GH release, with the greatest effect at 1 microM.
In plain wordsIn rat tumour cells that do not respond to GHRH, hexarelin raised growth hormone release, most at 1 microM.
- Peptide
- Hexarelin
- Outcome
- IncreaseGH release in GH1 cells
- Study
ratn: not reported in source
GH1 rat tumor cell line, insensitive to GHRH- Comparator
- Control wells
- Outcome group
- Growth hormone and IGF-1 · Endocrine and hormones
- Studied dose
- 0.01-1 microMAs given in this study (rat).
Measurements
- GH release
- 155 % vs control wells
- GH1 cells, 1 microM
Source sentences
The GHRP-6 analog hexarelin (0.01-1 microM) significantly stimulated GH release in both normal and GH1 rat cells.
2 context sentences(design, population, supporting numbers)
The greatest GH-releasing effect of hexarelin was observed with the 1 microM dose both in GH1 (155+/-25% vs. control wells) and in normal rat pituitary cells (185+/-23% vs. control wells).
The aim of the study was to assess for the first time the effect on GH secretion of the GHRP-6 analog, hexarelin, in the GH1 cells; moreover, we investigated the potential involvement of GHRH in the effects of hexarelin in the GH1 rat cell line.