フルテキストURL fulltext.pdf
著者 Asanuma, Masato| Miyazaki, Ikuko|
キーワード glutathione neuroprotection parkinsonism astrocyte region specificity striatum mesencephalon oxidative stress Nrf2 metallothionein serotonin 5-HT1A receptor
発行日 2021-08-13
出版物タイトル International Journal of Molecular Sciences
22巻
16号
出版者 MDPI
開始ページ 8689
ISSN 1422-0067
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2021 by the authors.
論文のバージョン publisher
PubMed ID 34445395
DOI 10.3390/ijms22168689
Web of Science KeyUT 000690633200001
関連URL isVersionOf https://doi.org/10.3390/ijms22168689
フルテキストURL fulltext20210831-4.pdf
著者 Masai, Kaori| Kuroda, Keita| Isooka, Nami| Kikuoka, Ryo| Murakami, Shinki| Kamimai, Sunao| Wang, Dengli| Liu, Keyue| Miyazaki, Ikuko| Nishibori, Masahiro| Asanuma, Masato|
キーワード methamphetamine dopamine neuron high mobility group box-1 hyperthermia inflammation neurotoxicity
備考 This is a post-peer-review, pre-copyedit version of an article published in Neurotoxicity Research. The final authenticated version is available online at: https://doi.org/10.1007/s12640-021-00402-5
This fulltext is available in Aug. 2022.|
発行日 2021-8-21
出版物タイトル Neurotoxicity Research
39巻
出版者 Springer Science and Business Media LLC
開始ページ 1511
終了ページ 1523
ISSN 1029-8428
NCID AA11570800
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2021 Springer Nature Switzerland AG
論文のバージョン author
PubMed ID 34417986
DOI 10.1007/s12640-021-00402-5
Web of Science KeyUT 000687003700001
関連URL isVersionOf https://doi.org/10.1007/s12640-021-00402-5
フルテキストURL fulltext.pdf
著者 Asanuma, Masato| Okumura-Torigoe, Nao| Miyazaki, Ikuko| Murakami, Shinki| Kitamura, Yoshihisa| Sendo, Toshiaki|
キーワード astrocyte neuroprotection region-specificity striatum mesencephalon oxidative stress 6-hydroxydopamine Nrf2 phase II detoxifying molecules
発行日 2019-01-30
出版物タイトル International Journal of Molecular Sciences
20巻
3号
出版者 MDPI
開始ページ 598
ISSN 1422-0067
NCID AA12038549
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
論文のバージョン publisher
PubMed ID 30704073
DOI 10.3390/ijms20030598
Web of Science KeyUT 000462412500142
関連URL isVersionOf https://doi.org/10.3390/ijms20030598
フルテキストURL fulltext.pdf
著者 Miyazaki, Ikuko| Asanuma, Masato|
キーワード astrocyte Parkinson’s disease dopaminergic neuron neuroinflammation neuroprotection alpha-synuclein mitochondria
発行日 2020-12-07
出版物タイトル Cells
9巻
12号
出版者 MDPI
開始ページ 2623
ISSN 2073-4409
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2020 by the authors.
論文のバージョン publisher
PubMed ID 33297340
DOI 10.3390/cells9122623
Web of Science KeyUT 000601806600001
関連URL isVersionOf https://doi.org/10.3390/cells9122623
フルテキストURL fulltext.pdf
著者 Kikuoka, Ryo| Miyazaki, Ikuko| Kubota, Natsuki| Maeda, Megumi| Kagawa, Daiki| Moriyama, Masaaki| Sato, Asuka| Murakami, Shinki| Kitamura, Yoshihisa| Sendo, Toshiaki| Asanuma, Masato|
発行日 2020-11-26
出版物タイトル Scientific Reports
10巻
1号
出版者 Nature Research
開始ページ 20698
ISSN 2045-2322
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © The Author(s) 2020
論文のバージョン publisher
PubMed ID 33244123
DOI 10.1038/s41598-020-77652-4
Web of Science KeyUT 000596329600054
関連URL isVersionOf https://doi.org/10.1038/s41598-020-77652-4
フルテキストURL fulltext.pdf
著者 Kidani, Naoya| Hishikawa, Tomohito| Hiramatsu, Masafumi| Nishihiro, Shingo| Kin, Kyohei| Takahashi, Yu| Murai, Satoshi| Sugiu, Kenji| Yasuhara, Takao| Miyazaki, Ikuko| Asanuma, Masato| Date, Isao|
キーワード apoptosis cerebral blood flow crossed cerebellar diaschisis ischemic stroke oxidative stress
発行日 2020-06-10
出版物タイトル International Journal of Molecular Sciences
21巻
11号
出版者 MDPI
開始ページ 4137
ISSN 1422-0067
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2020 by the authors.
論文のバージョン publisher
PubMed ID 32531947
DOI 10.3390/ijms21114137
Web of Science KeyUT 000543400300399
関連URL isVersionOf https://doi.org/10.3390/ijms21114137
フルテキストURL fulltext.pdf Table&Figs.pdf
著者 Miyazaki, Ikuko| Kikuoka, Ryo| Isooka, Nami| Takeshima, Mika| Sonobe, Kanau| Arai, Rei| Funakoshi, Hidemaru| Quin, Kyle E.| Smart, Smart| Zensho, Kazumasa| Asanuma, Masato|
キーワード Bisphenol A diglycidyl ether Epoxy resin Brain development Neuronal differentiation Anxiety behavior
備考 This fulltext is available in March 2021.|
発行日 2020-03-03
出版物タイトル Food and Chemical Toxicology
138巻
出版者 Pergamon
開始ページ 111235
ISSN 0278-6915
NCID AA10627174
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2020 Elsevier Ltd.
論文のバージョン author
PubMed ID 32142877
DOI 10.1016/j.fct.2020.111235
Web of Science KeyUT 000542938400012
関連URL isVersionOf https://doi.org/10.1016/j.fct.2020.111235
著者 Asanuma, Masato| Miyazaki, Ikuko| Francisco J., Diaz-Corrales| Higashi, Youichirou| Namba, Masayoshi| Ogawa, Norio|
発行日 2013-06-12
出版物タイトル PLOS ONE
8巻
6号
資料タイプ 学術雑誌論文
JaLCDOI 10.18926/AMO/53020
フルテキストURL 68_6_317.pdf
著者 Kasahara, Kyosuke| Miyoshi, Ko| Murakami, Shinki| Miyazaki, Ikuko| Asanuma, Masato|
抄録 In vertebrates, almost all somatic cells extend a single immotile cilium, referred to as a primary cilium. Increasing evidence suggests that primary cilia serve as cellular antennae in many types of tissues by sensing chemical or mechanical stimuli in the milieu surrounding the cells. In rodents an antibody to adenylyl cyclase 3 (AC3) has been widely used to label the primary cilia of neurons in vivo by immunostaining, whereas the lack of markers for the primary cilia of astrocytes has made it difficult to observe astrocytic primary cilia in vivo. Here, we obtained a visualization of astrocytic primary cilia in the mouse brain. In the somatosensory cortex, a large portion of neurons and astrocytes at postnatal day 10 (P10), and of neurons at P56 had AC3-positive primary cilia, whereas only approx. one-half of the astrocytes in the P56 mice carried primary cilia weakly positive for AC3. In contrast, the majority of astrocytes had ADP-ribosylation factor-like protein 13B (Arl13b)-positive primary cilia in the somatosensory cortex and other brain regions of P56 mice. The lengths of astrocytic primary cilia positive for Arl13b varied among the brain regions. Our data indicate that Arl13b is a noteworthy marker of astrocytic primary cilia in the brain.
キーワード primary cilia astrocyte ADP-ribosylation factor-like protein 13B
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2014-12
68巻
6号
出版者 Okayama University Medical School
開始ページ 317
終了ページ 322
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 CopyrightⒸ 2014 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 25519025
Web of Science KeyUT 000346882200001
著者 Murakami, Shinki| Miyazaki, Ikuko| Sogawa, Norio| Miyoshi, Ko| Asanuma, Masato|
発行日 2014-10
出版物タイトル Neurotoxicity Research
26巻
3号
資料タイプ 学術雑誌論文
JaLCDOI 10.18926/AMO/47009
フルテキストURL 65_5_279.pdf
著者 Miyoshi, Ko| Kasahara, Kyosuke| Miyazaki, Ikuko| Asanuma, Masato|
抄録 Almost all mammalian cells carry one primary cilium that functions as a biosensor for chemical and mechanical stimuli. Genetic damages that compromise cilia formation or function cause a spectrum of disorders referred to as ciliapathies. Recent studies have demonstrated that some pharmacological agents and extracellular environmental changes can alter primary cilium length. Renal injury is a well-known example of an environmental insult that triggers cilia length modification. Lithium treatment causes primary cilia to extend in several cell types including neuronal cells;this phenomenon is likely independent of glycogen synthase kinase-3β inhibition. In renal epithelial cell lines, deflection of the primary cilia by fluid shear shortens them by reducing the intracellular cyclic AMP level, leading to a subsequent decrease in mechanosensitivity to fluid shear. Primary cilium length is also influenced by the dynamics of actin filaments and microtubules through the levels of soluble tubulin in the cytosol available for primary cilia extension. Thus, mammalian cells can adapt to the extracellular environment by modulating the primary cilium length, and this feedback system utilizing primary cilia might exist throughout the mammalian body. Further investigation is required concerning the precise molecular mechanisms underlying the control of primary cilium length in response to environmental factors.
キーワード primary cilium length lithium cyclic AMP soluble tubulin intraflagellar transport
Amo Type Review
出版物タイトル Acta Medica Okayama
発行日 2011-10
65巻
5号
出版者 Okayama University Medical School
開始ページ 279
終了ページ 285
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 CopyrightⒸ 2011 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 22037264
Web of Science KeyUT 000296116400001
JaLCDOI 10.18926/AMO/40129
フルテキストURL 64_4_219.pdf
著者 Doi, Maho| Miyazaki, Ikuko| Nagamachi, Tomoko| Shinomiya, Kazuaki| Matsunaga, Hisashi| Sendo, Toshiaki| Kawasaki, Hiromu| Asanuma, Masato| Gomita, Yutaka| Kitamura, Yoshihisa|
抄録 We examined the influence of chronic adrenocorticotropic hormone (ACTH) treatment on the number of Ki-67-positive cells in the dentate gyrus of the hippocampus in rats. ACTH treatment for 14 days decreased the number of such cells. The administration of imipramine or lithium alone for 14 days had no effect in saline-treated rats. The effect of ACTH was blocked by the administration of imipramine. Furthermore, the coadministration of imipramine and lithium for 14 days significantly increased the number of Ki-67-positive cells in both the saline and ACTH-treated rats. The coadministration of imipramine and lithium normalized the cell proliferation in the dentate gyrus of the hippocampus in rats treated with ACTH.
キーワード ACTH imipramine lithium proliferation Ki-67
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2010-08
64巻
4号
出版者 Okayama University Medical School
開始ページ 219
終了ページ 223
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 20802538
Web of Science KeyUT 000281384400002
JaLCDOI 10.18926/AMO/32278
フルテキストURL fulltext.pdf
著者 Tanaka, Ken-ichi| Fujita, Naoko| Asanuma, Masato| Ogawa, Norio|
抄録

We examined the effects of FK506 and its non-immunosuppressive derivative, GPI1046, on H2O2-induced reduction of cell viability and apoptotic cell death in Neuro 2A cells. Our results suggest that the protective properties of GPI1046 against H2O2-induced reduction of cell viability are equipotent with those of FK506 and may be mediated by increased intracellular concentrations of glutathione (GSH). In addition, both FK506 and GPI1046 prevented apoptotic cell death in Neuro 2A cells, although the antiapoptotic effect of FK506 was somewhat stronger than that of GPI1046. These findings suggest that non-immunosuppressive immunophilin ligands such as GPI1046 might be potentially useful in treatment of neurodegenerative diseases without serious side effects such as immune deficiency.

キーワード hydrogen peroxide immunophilin ligands apoptosis glutathione FK506 GPI1046
Amo Type Article
出版物タイトル Acta Medica Okayama
発行日 2000-12
54巻
6号
出版者 Okayama University Medical School
開始ページ 275
終了ページ 280
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
論文のバージョン publisher
査読 有り
PubMed ID 11132921
Web of Science KeyUT 000166042900006
JaLCDOI 10.18926/AMO/32199
フルテキストURL fulltext.pdf
著者 Takayama, Haruhiko| Ogawa, Norio| Asanuma, Masato| Hirata, Hiroshi| Ogura, Toshio| Ota, Zensuke|
抄録

To gain further insight into the central nervous system (CNS)-action of beta-adrenergic blocking agents (beta-blockers), we examined the effects of various kinds of beta-blockers on opioid receptors (Op-Rs) using radiolabeled receptor assay (RRA). We demonstrated that beta-blockers are competitively bound to Op-Rs in the CNS. Sodium index of beta-blockers in [3H]naloxone binding study indicated that beta-blockers had the mixed agonist-antagonist activity of opiates. The relative potency of beta-blockers in opioid RRA was negatively correlated with their membrane stabilizing activity. Neither beta-blocking activity nor intrinsic sympathomimetic activity was correlated with IC50 values of beta-blockers in opioid RRA. While it is widely accepted that beta-blockers have a tranquilizing activity, a part of the tranquilizing action of beta-blockers may be mediated through Op-Rs in the CNS. Although beta-blockers may have effects on their own receptors (beta-receptors) in the CNS, the more precise mechanisms of central action of these drugs must be further investigated.

キーワード ?-blocker opioid receptor membrane stabilizing activity sodium index
Amo Type Article
出版物タイトル Acta Medica Okayama
発行日 1991-10
45巻
5号
出版者 Okayama University Medical School
開始ページ 295
終了ページ 299
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
論文のバージョン publisher
査読 有り
PubMed ID 1684486
Web of Science KeyUT A1991GN53800001
JaLCDOI 10.18926/AMO/32105
フルテキストURL fulltext.pdf
著者 Asanuma, Masato| Miyazaki, Ikuko| Diaz-Corrales, Francisco J| Ogawa, Norio|
抄録

Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by dopaminergic neuron-specific degeneration in the substantia nigra. A number of gene mutations and deletions have been reported to play a role in the pathogenesis of familial PD. Moreover, a number of pathological and pharmacological studies on sporadic PD and dopaminergic neurotoxin-induced parkinsonism have hypothesized that mitochondrial dysfunction, inflammation, oxidative stress, and dysfunction of the ubiquitin-proteasome system all play important roles in the pathogenesis and progress of PD. However, these hypotheses do not yet fully explain the mechanisms of dopaminergic neuron-specific cell loss in PD. Recently, the neurotoxicity of dopamine quinone formation by auto-oxidation of dopamine has been shown to cause specific cell death of dopaminergic neurons in the pathogenesis of sporadic PD and dopaminergic neurotoxin-induced parkinsonism. Furthermore, this quinone formation is closely linked to other representative hypotheses in the pathogenesis of PD. In this article, we mainly review recent studies on the neurotoxicity of quinone formation as a dopaminergic neuron-specific oxidative stress and its role in the etiology of PD, in addition to several neuroprotective approaches against dopamine quinone-induced toxicity.

キーワード dopamine quinone quinoprotein Parkinson’sdisease oxidative stress neurotoxin
Amo Type Article
出版物タイトル Acta Medica Okayama
発行日 2004-10
58巻
5号
出版者 Okayama University Medical School
開始ページ 221
終了ページ 233
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
論文のバージョン publisher
査読 有り
PubMed ID 15666991
Web of Science KeyUT 000224708800001
JaLCDOI 10.18926/AMO/32031
フルテキストURL fulltext.pdf
著者 Aoki, Sogawa Chiharu| Asanuma, Masato| Sogawa, Norio| Miyazaki, Ikuko| Nakanishi, Tohru| Furuta, Hiroaki| Ogawa, Noriko|
抄録

The metallothionein (MT) family is a class of low molecular, intracellular, and cysteine-rich proteins with a high affinity for metals. Although the first of these proteins was discovered nearly 40 years ago, their functional significance remains obscure. Four major isoforms (MT-I, MT-II, MT-III, and MT-IV) have been identified in mammals. MT-I and MT-II are ubiquitously expressed in various organs including the brain, while expression of MT-III and MT-IV is restricted in specific organs. MT-III was detected predominantly in the brain, and characterized as a central nervous system-specific isomer. The role of MTs in the central nervous system has become an intense focus of scientific research. An isomer of MTs, MT-III, of particular interest, was originally discovered as a growth inhibitory factor, and has been found to be markedly reduced in the brain of patients with Alzheimer's disease and several other neurodegenerative diseases. MT-III fulfills unique biological roles in homeostasis of the central nervous system and in the etiology of neuropathological disorders.

キーワード neuroprotectin metal transport localization gene expression neurodegenerative disease
Amo Type Review
出版物タイトル Acta Medica Okayama
発行日 2001-02
55巻
1号
出版者 Okayama University Medical School
開始ページ 1
終了ページ 9
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
論文のバージョン publisher
査読 有り
PubMed ID 11246971
Web of Science KeyUT 000167249900001
JaLCDOI 10.18926/AMO/30980
フルテキストURL fulltext.pdf
著者 Miyazaki, Ikuko| Asanuma, Masato|
抄録

Oxidative stress, including the reactive oxygen or nitrogen species generated in the enzymatical oxidationor auto-oxidation of an excess amount of dopamine, is thought to play an important role in dopaminergic neurotoxicity. Dopamine and its metabolites containing 2 hydroxyl residues exert cytotoxicityin dopaminergic neuronal cells, primarily due to the generation of highly reactive dopamine and DOPA quinones. Dopamine and DOPA quinones may irreversibly alter protein function through the formation of 5-cysteinyl-catechols on the proteins. Furthermore, the quinone formation is closely linked to other representative hypotheses such as mitochondrial dysfunction, inflammation, oxidative stress, and dysfunction of the ubiquitin-proteasome system, in the pathogenesis of neurodegenerative diseases. Therefore, pathogenic effects of the dopamine quinone have recently focused on dopaminergicneuron-specific oxidative stress. In this article, we primarily review recent studies on the pathogenicity of quinone formation, in addition to several neuroprotective approaches against dopaminequinone-induced dysfunction of dopaminergic neurons.

キーワード dopamine quinone quinoprotein methamphetamine Parkinson?s disease L-DOPA
Amo Type Review
出版物タイトル Acta Medica Okayama
発行日 2008-06
62巻
3号
出版者 Okayama University Medical School
開始ページ 141
終了ページ 150
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
論文のバージョン publisher
査読 有り
PubMed ID 18596830
Web of Science KeyUT 000257130300001
JaLCDOI 10.18926/AMO/30724
フルテキストURL Fulltext.pdf erratum_61_2_121.pdf
著者 Fujita, Osamu| Asanuma, Masato| Yokoyama, Teruhiko| Miyazaki, Ikuko| Ogawa, Norio| Kumon, Hiromi|
抄録 We examined the involvement of the signal transducer and activator of transcription 3 (STAT3) in bladder outlet obstruction (BOO)-induced bladder smooth muscle hypertrophy using a rat in vivo and in vitro study. BOO induced increases in bladder weight and bladder smooth muscle thickness 1 week after the operation. By using antibody microarrays, 64 of 389 proteins blotted on the array met our selection criteria of an INR value between > or = 2.0 and < or = 0.5. This result revealed up-regulation of transcription factors, cell cycle regulatory proteins, apoptosis-associated proteins and so on. On the other hand, down-regulation (INR value < or = 0.5) of proteins was not found. In a profiling study, we found an increase in the expression of STAT3. A significant increase in nuclear phosphorylated STAT3 expression was confirmed in bladder smooth muscle tissue by immunohistochemistry and Western blot analysis. Cyclical stretch-relaxation (1 Hz) at 120% elongation significantly increased the expression of STAT3 and of alpha-smooth muscle actin in primary cultured bladder smooth muscle cells. Furthermore, the blockade of STAT3 expression by the transfection of STAT3 small interfering RNA (siRNA) significantly prevented the stretch-induced increase in alpha-smooth muscle actin expression. These results suggest that STAT3 has an important role in the induction of bladder smooth muscle hypertrophy.
キーワード benign prostatic hyperplasia bladder outlet obstruction bladder smooth muscle signal transducer and activator of transcription 3 (STAT3) small interfering RNA (siRNA)
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2006-12
60巻
6号
出版者 Okayama University Medical School
開始ページ 299
終了ページ 309
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
論文のバージョン publisher
査読 有り
PubMed ID 17189973
Web of Science KeyUT 000243019000001
著者 宮崎 育子| 浅沼 幹人| Francisco J. Diaz-Corrales| 三好 耕| 小川 紀雄|
発行日 2008-01-04
出版物タイトル 岡山医学会雑誌
119巻
3号
資料タイプ 学術雑誌論文
著者 淺沼 幹人|
発行日 1992-03-31
出版物タイトル
資料タイプ 学位論文