X. Chen, W. Pan, The Treatment Strategies for Neurodegenerative Diseases by Integrative Medicine. Integr. Med. Int. 1(4), 223–225 (2015). https://doi.org/10.1159/000381546
T.J. Moore, H. Abrahamse, Neuronal Differentiation of Adipose-Derived Stem Cells: Progress So Far. Int. J. Photoenergy. 1–8 (2014). https://doi.org/10.1155/2014/827540
M.A. Ajmone-Cat, A. Bernardo, A. Greco, L. Minghetti, Non-Steroidal Anti-Inflammatory Drugs and Brain Inflammation: Effects on Microglial Functions. Pharmceuticals 3(6), 1949–1965 (2010). https://doi.org/10.3390/ph3061949
M. Terzi, G. Altun, S. Şen, A. Kocaman, A.A. Kaplan, K.K. Yurt, S. Kaplan, The use of non-steroidal anti-inflammatory drugs in neurological diseases. J. Chem. Neuroanat. 87, 12–24 (2018). https://doi.org/10.1016/j.jchemneu.2017.03.003
Article CAS PubMed Google Scholar
K.P. Townsend, D. Praticò, Novel therapeutic opportunities for Alzheimer’s disease: focus on nonsteroidal anti-inflammatory drugs. FASEB J. 19(12), 1592–1601 (2005). https://doi.org/10.1096/fj.04-3620rev
Article CAS PubMed Google Scholar
B.A. in t’ Veld, A. Ruitenberg, A. Hofman, L.J. Launer, C.M. van Duijn, T. Stijnen, M.M. Breteler, B.H. Stricker, Nonsteroidal antiinflammatory drugs and the risk of Alzheimer’s disease. N. Engl. J. Med. 345(21), 1515–1521 (2001). https://doi.org/10.1056/NEJMoa010178
K.D. Rainsford, Safety and Efficacy of Non-prescription, Over-the-counter (OTC) Ibuprofen. In Ibuprofen: Discovery, Development and Therapeutics. John Wiley. 313–345, (2015). https://doi.org/10.1002/9781118743614.ch7.
P.H. Ashjian, A.S. Elbarbary, B. Edmonds, D. DeUgarte, M. Zhu, P.A. Zuk, H.P. Lorenz, P. Benhaim, M.H. Hedrick, In vitro differentiation of human processed lipoaspirate cells into early neural progenitors. Plast. Reconstr. Surg. 111(6), 1922–1931 (2003). https://doi.org/10.1097/01.PRS.0000055043.62589.05
J.A. McGuiness, R.B. Scheinert, A. Asokan, V.C. Stadler, C.S. Lee, A. Rani, A. Kumar, T.C. Foster, B.K. Ormerod, Indomethacin Increases Neurogenesis across Age Groups and Improves Delayed Probe Trial Difference Scores in Middle-Aged Rats. Front. Aging Neurosci. 9, 280 (2017). https://doi.org/10.3389/fnagi.2017.00280
Article CAS PubMed PubMed Central Google Scholar
E.G. Hain, M. Sparenberg, J. Rasińska, C. Klein, L. Akyüz, B. Steiner, Indomethacin promotes survival of new neurons in the adult murine hippocampus accompanied by anti-inflammatory effects following MPTP-induced dopamine depletion. J. Neuroinflammation 15(1), 162 (2018). https://doi.org/10.1186/s12974-018-1179-4
Article CAS PubMed PubMed Central Google Scholar
Y. Zhang, X. Wang, S.V. Baranov, S. Zhu, Z. Huang, W. Fellows-Mayle, J. Jiang, A.L. Day, B.S. Kristal, R.M. Friedlander, Dipyrone inhibits neuronal cell death and diminishes hypoxic/ischemic brain injury. Neurosurgery 69(4), 942–956 (2011). https://doi.org/10.1227/NEU.0b013e318222afb2
E.F. Collares, L.E.A. Troncon, Effects of dipyrone on the digestive tract. Braz. J. Med. Biol. Res. 52(2), e8103 (2019). https://doi.org/10.1590/1414-431X20188103
Article CAS PubMed PubMed Central Google Scholar
M. Fukuchi, Identifying inducers of BDNF gene expression from pharmacologically validated compounds; antipyretic drug dipyrone increases BDNF mRNA in neurons. Biochem. Biophys. Res. Commun. 524(4), 957–962 (2020). https://doi.org/10.1016/j.bbrc.2020.02.019
Article CAS PubMed Google Scholar
I. Nikolova, L. Marinov, A. Georgieva, R. Toshkova, M. Malchev, Y. Voynikov, I. Kostadinova, Metamizole (dipyrone) – cytotoxic and antiproliferative effects on HeLa, HT-29 and MCF-7 cancer cell lines. Biotechnol. Biotechnological Equip. 32(5), 1327–1337 (2018). https://doi.org/10.1080/13102818.2018.1511382
E. Maytalman, D.N. Samur, O.C. Gunizi, I. Kozanoglu, The effects of metamizole on hematopoietic progenitor cells: Suppression of hematopoiesis stimulation in vitro. Bratisl. Lek. Listy 124(4), 320–329 (2023). https://doi.org/10.4149/BLL_2023_049
D. Mizuno, K. Konoha-Mizuno, M. Mori, K. Yamazaki, T. Haneda, H. Koyama, M. Kawahara, An In Vitro System Comprising Immortalized Hypothalamic Neuronal Cells (GT1-7 Cells) for Evaluation of the Neuroendocrine Effects of Essential Oils. Evid. Based Complement Altern. Med 2015, 343942 (2015). https://doi.org/10.1155/2015/343942
L. Casati, S. Ciceri, R. Maggi, D. Bottai, Physiological and pharmacological overview of the gonadotropin releasing hormone. Biochem. Pharm. 212, 115553 (2023). https://doi.org/10.1016/j.bcp.2023.115553
Article CAS PubMed Google Scholar
B. Connor, M. Dragunow, The role of neuronal growth factors in neurodegenerative disorders of the human brain. Brain Res. Rev. 27(1), 1–39 (1998). https://doi.org/10.1016/s0165-0173(98)00004-6
Article CAS PubMed Google Scholar
F. Martorana, D. Gaglio, M.R. Bianco, F. Aprea, A. Virtuoso, M. Bonanomi, L. Alberghina, M. Papa, A.M. Colangelo, Differentiation by nerve growth factor (NGF) involves crosstalk mechanisms between energy homeostasis and mitochondrial remodeling. Cell Death Dis. 9(3), 391 (2018). https://doi.org/10.1038/s41419-018-0429-9
Article CAS PubMed PubMed Central Google Scholar
J. Biane, J.M. Conner, M.H. Tuszynski, Nerve growth factor is primarily produced by GABAergic neurons of the adult rat cortex. Front. Cell Neurosci. 8, 220 (2014). https://doi.org/10.3389/fncel.2014.00220
Article PubMed PubMed Central Google Scholar
J. Luo, Y. Yang, T. Zhang, Z. Su, D. Yu, Q. Lin, H. Chen, Q. Zhang, Q. Xiang, W. Xue, R. Ge, Y. Huang, Nasal delivery of nerve growth factor rescue hypogonadism by up-regulating GnRH and testosterone in aging male mice. EBioMedicine 35, 295–306 (2018). https://doi.org/10.1016/j.ebiom.2018.08.021
Article PubMed PubMed Central Google Scholar
M.H. Ratto, L. Paiva, R. Carrasco, M.E. Silva, C. Ulloa-Leal, V.F. Ratto, J. Goicochea, Review: Unveiling the effect of beta-nerve growth factor on the reproductive function in llamas and cows. Animal 17(Suppl 1), 100754 (2023). https://doi.org/10.1016/j.animal.2023.100754
Article CAS PubMed Google Scholar
F. Pimpinelli, E. Redaelli, R. Restano-Cassulini, G. Curia, P. Giacobini, A. Cariboni, E. Wanke, G.P. Bondiolotti, F. Piva, R. Maggi, Depolarization differentially affects the secretory and migratory properties of two cell lines of immortalized luteinizing hormone-releasing hormone (LHRH) neurons. Eur. J. Neurosci. 18(6), 1410–1418 (2003). https://doi.org/10.1046/j.1460-9568.2003.02866.x
S. Suzuki, J. Namiki, S. Shibata, Y. Mastuzaki, H. Okano, The neural stem/progenitor cell marker nestin is expressed in proliferative endothelial cells, but not in mature vasculature. J. Histochem. Cytochem. 58(8), 721–730 (2010). https://doi.org/10.1369/jhc.2010.955609
Article CAS PubMed PubMed Central Google Scholar
M.L. Hendrickson, A.J. Rao, O.N. Demerdash, R.E. Kalil, Expression of nestin by neural cells in the adult rat and human brain. PLoS One 6(4), e18535 (2011). https://doi.org/10.1371/journal.pone.0018535
Article CAS PubMed PubMed Central Google Scholar
R.G. Romanelli, T. Barni, M. Maggi, M. Luconi, P. Failli, A. Pezzatini, E. Pelo, F. Torricelli, C. Crescioli, P. Ferruzzi, R. Salerno, M. Marini, C.M. Rotella, G.B. Vannelli, Expression and function of gonadotropin-releasing hormone (GnRH) receptor in human olfactory GnRH-secreting neurons: an autocrine GnRH loop underlies neuronal migration. J. Biol. Chem. 279(1), 117–126 (2004). https://doi.org/10.1074/jbc.M307955200
Article CAS PubMed Google Scholar
E.M. Jouhilahti, S. Peltonen, J. Peltonen, Class III beta-tubulin is a component of the mitotic spindle in multiple cell types. J. Histochem. Cytochem. 56(12), 1113–1119 (2008). https://doi.org/10.1369/jhc.2008.952002
Article CAS PubMed PubMed Central Google Scholar
E. Dráberová, L. Del Valle, J. Gordon, V. Marková, B. Smejkalová, L. Bertrand, J.P. de Chadarévian, D.P. Agamanolis, A. Legido, K. Khalili, P. Dráber, C.D. Katsetos, Class III beta-tubulin is constitutively coexpressed with glial fibrillary acidic protein and nestin in midgestational human fetal astrocytes: implications for phenotypic identity. J. Neuropathol. Exp. Neurol. 67(4), 341–354 (2008). https://doi.org/10.1097/NEN.0b013e31816a686d
S.A. Malone, G.E. Papadakis, A. Messina, N.E.H. Mimouni, S. Trova, M. Imbernon, C. Allet, I. Cimino, J. Acierno, D. Cassatella, C. Xu, R. Quinton, G. Szinnai, P. Pigny, L. Alonso-Cotchico, L. Masgrau, J.D. Maréchal, V. Prevot, N. Pitteloud, P. Giacobini, Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism. Elife 8, e47198 (2019). https://doi.org/10.7554/eLife.47198
Article CAS PubMed PubMed Central Google Scholar
P.I. Lorenzo, C. Ménard, F.D. Miller, J. Bernal, Thyroid hormone-dependent regulation of Talpha1 alpha-tubulin during brain development. Mol. Cell Neurosci. 19(3), 333–343 (2002). https://doi.org/10.1006/mcne.2001.1087
Article CAS PubMed Google Scholar
P.R. Kramer, S. Wray, Midline nasal tissue influences nestin expression in nasal-placode-derived luteinizing hormone-releasing hormone neurons during development. Dev. Biol. 227(2), 343–357 (2000). https://doi.org/10.1006/dbio.2000.9896
Article CAS PubMed Google Scholar
R. Tsutsumi, N.J. Webster, GnRH pulsatility, the pituitary response and reproductive dysfunction. Endocr. J. 56(6), 729–737 (2009). https://doi.org/10.1507/endocrj.k09e-185
Article CAS PubMed PubMed Central Google Scholar
N. Wickramasuriya, R. Hawkins, C. Atwood, T. Butler, The roles of GnRH in the human central nervous system. Horm. Behav. 145, 105230 (2022). https://doi.org/10.1016/j.yhbeh.2022.105230
留言 (0)