Title Genistein Antagonizes 17 beta-Estradiol Effects on Glutamate-Evoked Masseter Muscle Hypernociception in Rats
Authors Jie, Hui-Fei
Yang, Guang-Ju
Bi, Rui-Yun
Mo, Si-Yi
Gan, Ye-Hua
Xie, Qiu-Fei
Affiliation Peking Univ, Sch & Hosp Stomatol, Dept Prosthodont, Beijing, Peoples R China.
Peking Univ, Sch & Hosp Stomatol, Ctr Oral Funct Diag Treatment & Res, Beijing, Peoples R China.
Peking Univ, Sch & Hosp Stomatol, Dent Ctr 3, Beijing, Peoples R China.
Peking Univ, Sch & Hosp Stomatol, Cent Lab, Beijing, Peoples R China.
Peking Univ, Sch & Hosp Stomatol, Ctr TMD & Orofacial Pain, Beijing, Peoples R China.
Peking Univ, Sch & Hosp Stomatol, Dept Prosthodont, Beijing, Peoples R China.
Xie, QF (reprint author), Peking Univ, Sch & Hosp Stomatol, Ctr Oral Funct Diag Treatment & Res, Beijing, Peoples R China.
Gan, YH (reprint author), Peking Univ, Sch & Hosp Stomatol, Cent Lab, Beijing, Peoples R China.
Gan, YH (reprint author), Peking Univ, Sch & Hosp Stomatol, Ctr TMD & Orofacial Pain, Beijing, Peoples R China.
Keywords genistein
17 beta-estradiol
orofacial pain
NMDAR
ERK1/2
hippocampus
TEMPOROMANDIBULAR-JOINT INFLAMMATION
CORD DORSAL-HORN
NMDA RECEPTOR
SPINAL-CORD
PAIN HYPERSENSITIVITY
OVARIECTOMIZED RATS
INDUCED NOCICEPTION
UP-REGULATION
NR1 SUBUNIT
MAP KINASE
Issue Date 2018
Publisher FRONTIERS IN NEUROLOGY
Citation FRONTIERS IN NEUROLOGY. 2018, 9.
Abstract Temporomandibular disorders (TMDs) predominantly affect women of reproductive ages, with pain as the mains symptom. The aim of the present study was to examine the effects of 17 beta-estradiol (E2) on glutamate-evoked hypernociception of masseter muscle and to examine whether genistein could antagonize the effects of E2 in female rats. Injection of glutamate into the masseter muscle dose-dependently decreased head withdrawal thresholds, a parameter for mechanical hypernociception. Head withdrawal thresholds in ovariectomized rats also decreased with increasing doses of E2 replacement, and were further aggravated by injection of glutamate (1M, 40 mu L) into the masseters. Genistein at doses of 7.5 and 15 mg/kg antagonized E2-induced hypernociception of masseter muscle, and at doses of 7.5, 15, and 30 mg/kg also antagonized E2 potentiation of glutamate-evoked hypernociception of masseter muscle. Genistein produced optimal antagonistic effects of E2 on nociception behavior at a dose of 15 mg/kg. On the molecular level, tyrosine phosphorylation of the NR2B subunit of the N-methyl-D-aspartate receptor (pNR2B) and phosphorylated mitogen-activated protein kinase (pERK1/2) were significantly upregulated in the hippocampus following glutamate injection and were further potentiated by E2 replacement. Genistein at dose of 15 mg/kg partially reversed E2-potentiated glutamate-evoked upregulation of pNR2B and pERK1/2 expression in the hippocampus. These results indicated that moderate doses of genistein could antagonize E2 enhanced glutamate-evoked hypernociception of masseter muscle possibly via N-methyl-D-aspartate receptor and ERK1/2 signaling pathways in the hippocampus.
URI http://hdl.handle.net/20.500.11897/517870
ISSN 1664-2295
DOI 10.3389/fneur.2018.00649
Indexed SCI(E)
PubMed
Medline
Appears in Collections: 口腔医院

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