» Articles » PMID: 16574776

Growth Hormone is Produced Within the Hippocampus Where It Responds to Age, Sex, and Stress

Overview
Specialty Science
Date 2006 Apr 1
PMID 16574776
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

Recent studies by our group and others have demonstrated that growth hormone (GH) is produced endogenously within the hippocampal formation, a brain structure associated with learning and aspects of emotional experience. Here, we demonstrate that this endogenously produced GH is modulated by age and sex differences and the presence of estrogen. GH mRNA levels were higher in females than males, especially during proestrus, a stage of estrus when estrogen levels are elevated. Moreover, GH expression was increased in ovariectomized females that were treated with estradiol. This increase in GH mRNA in response to estrogen was followed by the appearance of GH protein and was negatively correlated with the expression levels of insulin-like growth factor-I mRNA, suggesting a feedback relationship between insulin-like growth factor-I and GH in the brain. GH mRNA levels were also elevated in primary neuronal cultures exposed to 17-beta-estradiol in vitro, further confirming the direct influence of estrogen on GH expression. Finally, exposure to an acute stressful event increased the expression and production of GH in both males and females. However, the stress-induced increase of GH in females depended on the stage of the estrous cycle in which they were exposed to the stressful event. Together, these data further demonstrate that GH is endogenously produced in the adult hippocampal formation, where it is regulated by age, estrogen, and exposure to environmental stimuli. These results suggest that GH may be involved in functions ascribed to the hippocampus, such as learning and the response to stressful experience.

Citing Articles

The effect of growth hormone on motor findings and dendrite morphology in an experimental Parkinson's disease model.

Kirazli O, Ozkan M, Verimli U, Gulhan R, Arman A, Sehirli U Anat Sci Int. 2024; 100(1):79-87.

PMID: 39085683 DOI: 10.1007/s12565-024-00790-6.


The metabolic effects of resumption of a high fat diet after weight loss are sex dependent in mice.

Guerra-Cantera S, Frago L, Jimenez-Hernaiz M, Collado-Perez R, Canelles S, Ros P Sci Rep. 2023; 13(1):13227.

PMID: 37580448 PMC: 10425431. DOI: 10.1038/s41598-023-40514-w.


Non-pituitary GH regulation of the tissue microenvironment.

Chesnokova V, Melmed S Endocr Relat Cancer. 2023; 30(7).

PMID: 37066857 PMC: 10247477. DOI: 10.1530/ERC-23-0028.


The multiple roles of GH in neural ageing and injury.

Blackmore D, Waters M Front Neurosci. 2023; 17:1082449.

PMID: 36960169 PMC: 10027725. DOI: 10.3389/fnins.2023.1082449.


Aberrant glial activation and synaptic defects in CaMKIIα-iCre and nestin-Cre transgenic mouse models.

Alia A, Jeon S, Popovic J, Salvo M, Sadleir K, Vassar R Sci Rep. 2022; 12(1):22099.

PMID: 36543864 PMC: 9772212. DOI: 10.1038/s41598-022-26671-4.


References
1.
Aberg M, Aberg N, Hedbacker H, Oscarsson J, Eriksson P . Peripheral infusion of IGF-I selectively induces neurogenesis in the adult rat hippocampus. J Neurosci. 2001; 20(8):2896-903. PMC: 6772218. View

2.
Sonntag W, Ramsey M, Carter C . Growth hormone and insulin-like growth factor-1 (IGF-1) and their influence on cognitive aging. Ageing Res Rev. 2005; 4(2):195-212. DOI: 10.1016/j.arr.2005.02.001. View

3.
Kopchick J, Andry J . Growth hormone (GH), GH receptor, and signal transduction. Mol Genet Metab. 2000; 71(1-2):293-314. DOI: 10.1006/mgme.2000.3068. View

4.
Hull K, Harvey S . Growth hormone: a reproductive endocrine-paracrine regulator?. Rev Reprod. 2000; 5(3):175-82. DOI: 10.1530/ror.0.0050175. View

5.
Nyberg F . Growth hormone in the brain: characteristics of specific brain targets for the hormone and their functional significance. Front Neuroendocrinol. 2000; 21(4):330-48. DOI: 10.1006/frne.2000.0200. View