Results 71 to 80 of about 8,222 (228)

Chicken LEAP2 Level Substantially Changes with Feed Intake and May Be Regulated by CDX4 in Small Intestine

Animals, 2022
Ghrelin O-acyltransferase (GOAT), ghrelin, and GHSR have been reported to play important roles that influence feed intake in mammals. LEAP2, an endogenous antagonist of GHSR, plays an important role in the regulation of feed intake.
Xiaotong Zheng, Ziwei Chen, Wuchao Zhuang, Jilong Zhang, Jiaheng He, Yinku Xie, Jianfei Chen   +6 more
doaj   +1 more source

Obesity-Induced PVAT Dysfunction and Atherosclerosis Development: The Role of GHSR-1a in Increased Macrophage Infiltration and Adipocytokine Secretion. [PDF]

J Cardiovasc Dev Dis
In obesity, recent research revealed that increased expression of the growth hormone secretagogue receptor (GHSR) in macrophages plays a pivotal role in the development of meta-inflammation, promoting macrophage infiltration and pro-inflammatory ...
Peiu SN, Zugun-Eloae F, Stoica B, Anisie E, Iosep DG, Danciu M, Silivestru-Crețu I, Akad F, Avadanei AN, Condur L, Popa RF, Mocanu V.   +11 more
europepmc   +2 more sources

Smartphone based music intervention in the treatment of episodic migraine headaches – A pilot trial

Complementary Therapies in Medicine, 2021
Objectives: Migraine headaches are a prevalent and burdening disorder for the public worldwide. Both traditional preventive drugs and behavioral-based interventions have been used as treatment in the prevention of migraine attacks.
Guilhem Parlongue, Emmanuelle Vuillaume Cerdan, Julian Koenig, DeWayne P. Williams   +3 more
doaj   +1 more source

Stress‐induced hyperphagia? Characterising the activity of the ghrelin axis in male rats with high anxiety behaviour

Journal of Neuroendocrinology, Volume 38, Issue 1, January 2026.
Abstract While evidence is emerging that the temporal pattern of feeding may influence anxiety, it is unclear to what extent anxiety may itself impact spontaneous feeding behaviour. To address this, we have quantified spontaneous feeding, ghrelin secretion and adult hippocampal neurogenesis (AHN) in male low (LAB) and high (HAB) anxiety‐behaviour rats.
Amanda K. E. Hornsby, Bradley Haywood‐Sheldrake, Katharina Gryksa, Andrea Havasi, Luke D. Roberts, Trevor Humby, Inga D. Neumann, Jeffrey S. Davies, Timothy Wells   +8 more
wiley   +1 more source

Nucleotide polymorphisms of the bovine growth hormone secretagogue receptor 1a (GHSR1a) gene and their association with growth and carcass traits in Japanese Black cattle [PDF]

, 2010
Ghrelin growth hormone secretagogue receptor 1a (GHSR1a) is involved in many important functions, including growth hormone secretion and food intake (Howard et al. 1996).
Fujimori, Y, Itoh, T, Komatsu, M, Malau-Aduli, AEO, Sato, Y, Satoh, M, Takahashi, H   +6 more
core   +3 more sources

The gatekeepers of growth: The neural roles and regulation of growth hormone‐releasing hormone neurons

Journal of Neuroendocrinology, Volume 38, Issue 1, January 2026.
Abstract The neuroendocrine control of growth is mediated by the hypothalamic–pituitary–somatic (HPS) axis. This involves the hypothalamic release of growth hormone‐releasing hormone (GHRH), which stimulates the pituitary secretion of growth hormone (GH).
Bradley B. Jamieson
wiley   +1 more source

Endogenous production of ghrelin and beneficial effects of its exogenous administration in monocrotaline-induced pulmonary hypertension [PDF]

, 2004
We investigated the endogenous production of ghrelin as well as cardiac and pulmonary vascular effects of its administration in a rat model of monocrotaline (MCT)-induced pulmonary hypertension (PH).
Baptista, MJ, Brandão-Nogueira, A, Correia-Pinto, J, Fortunato, JM, Henriques-Coelho, T, Leite-Moreira, AF, Lourenço, AP, Oliveira, SM, Roncon-Albuquerque R, Jr., Teles, A   +9 more
core   +1 more source

Enhanced Growth and Immune Response in Common Carp Fry (Cyprinus carpio) Treated With a Novel Growth Hormone‐Releasing Peptide Analog (F5WAC)

Aquaculture Research, Volume 2026, Issue 1, 2026.
Growth hormone (GH)‐releasing peptides (GHRPs) regulate growth and immune responses in fish, offering potential aquaculture applications. This study evaluated the effects of GHRP‐6 and its recombinant analog, F5WAC (acetylation of the N‐terminal Histidine [His1] and substitution of D‐Phenylalanine with D‐Tryptophan at position 5), on growth performance,
AbdolMajid Valipour, Behrooz Heidari, Sorour Ramezanpour, Navid Omidian   +3 more
wiley   +1 more source

Expression of Ghrelin and GHSR-1a in Long Term Diabetic Rat's Kidney [PDF]

Brazilian Archives of Biology and Technology, 2016
The aim of this work was to study the relative ghrelin and growth hormone secretagogue receptor (GHS-R)1a gene expression in the kidney of long-term diabetic rats. Forty male Wistar albino rats were divided into four groups: C- control group, DI- one month diabetic rats group, DII- two months diabetic rats group, and DIII- three months diabetic rats ...
Yildirim, Aysegul Burcin, Karabulut, Derya, Dundar, Munis, Ulusoy, Hasan Basri, Sonmez, Mehmet Fatih   +4 more
openaire   +4 more sources

Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits [PDF]

, 2016
The growth hormone/insulin-like growth factor (IGF) axis can be manipulated in animal models to promote longevity, and IGF-related proteins including IGF-I and IGF-binding protein-3 (IGFBP-3) have also been implicated in risk of human diseases including ...
Aschard, H. (Hugues), Bandinelli, S. (Stefania), Beekman, M. (Marian), Berndt, S.I. (Sonja), Bidlingmaier, M. (Martin), Broer, L. (Linda), Cappola, A.R. (Anne), Ceda, G.P. (Gian Paolo), Chanock, S.J. (Stephen), Chen, M.-H. (Ming-Huei), Chen, T.C. (Tai C.), Chen, Y.D. (Y.), Chung, J. (Jonathan), Del Greco Miglianico, F. (Fabiola), Duijn, C.M. (Cornelia) van, Eriksson, J. (Joel), Ferrucci, L. (Luigi), Friedrich, N. (Nele), Gnewuch, C. (Carsten), Goodarzi, M. (Mark), Grarup, N. (Niels), Guo, T. (Tingwei), Hammer, E. (Elke), Hayes, R.B. (Richard), Heemst, D. (Diana) van, Hicks, A.A. (Andrew), Hofman, A. (Albert), Houwing-Duistermaat, J.J. (Jeanine), Hu, F. (Frank), Hunter, D. (David), Husemoen, L.L.N. (Lise Lotte), Isaacs, A.J. (Aaron), Jacobs, K.B. (Kevin), Janssen, J.A.M.J.L. (Joop), Jansson, J.-O. (John-Olov), Jehmlich, N. (Nico), Johnson, S. (Simon), Juul, A. (Anders), Kaplan, R.C. (Robert), Karlsson, M. (Magnus), Kilpeläinen, T.O. (Tuomas), Kovacs, P. (Peter), Kraft, P. (Peter), Li, C. (Chao), Linneberg, A. (Allan), Liu, Y. (YongMei), Loos, R.J.F. (Ruth), Lorentzon, M. (Mattias), Lu, Y. (Yingchang), Maggio, M. (Marcello), Meigs, J.B. (James), Mellström, D. (Dan), Mägi, R. (Reedik), Nauck, M. (Matthias), Nethander, M. (Maria), Newman, A.B. (Anne B.), Ohlsson, C. (Claes), Pollak, M.N. (Michael), Pramstaller, P.P. (Peter Paul), Prokopenko, I. (Inga), Psaty, B.M. (Bruce), Qi, Q., Reincke, M. (Martin), Rimm, E.B. (Eric B.), Rotter, J.I. (Jerome I.), Saint Pierre, A. (Aude), Schurmann, C. (Claudia), Seshadri, S. (Sudha), Sjögren, K. (Klara), Slagboom, P.E. (Eline), Strickler, H.D. (Howard D.), Stumvoll, M. (Michael), Suh, Y. (Yousin), Sun, Q. (Qi), Svensson, J. (Johan), Tanaka, T. (Toshiko), Tare, A. (Archana), Teumer, A. (Alexander), Tönjes, A. (Anke), Uh, H.-W. (Hae-Won), Vandenput, L. (Liesbeth), Vasan, R.S. (Ramachandran Srini), Völker, U. (Uwe), Wallaschofski, H. (Henri), Willems, S.M. (Sara), Zhang, C. (Cuilin)   +85 more
core   +1 more source