Updated on 2024/07/15

写真a

 
Yasu-Taka Azuma
 
Organization
Graduate School of Veterinary Science Department of Veterinary Science Professor
School of Veterinary Science Department of Veterinary Science
Title
Professor
Affiliation
Institute of Veterinary Science
Affiliation campus
Rinku Campus

Position

  • Graduate School of Veterinary Science Department of Veterinary Science 

    Professor  2022.04 - Now

  • School of Veterinary Science Department of Veterinary Science 

    Professor  2022.04 - Now

Degree

  • 博士(獣医学)

  • 博士(歯学) ( Others )

  • 修士(薬学) ( Others )

Research Areas

  • Life Science / Immunology  / Inflammatory Disease

  • Life Science / Gastroenterology  / Inflammatory Bowel Disease

  • Life Science / Veterinary medical science  / Mucosal Immunology

  • Life Science / Pharmacology

Research Interests

  • NASH・肝炎

  • 炎症性腸疾患

  • Cytokine

  • Macrophage

  • 臓器連関

  • 炎症性疾患

  • 消化器疾患

  • マウス病態モデル

  • インターロイキン-19(IL-19)

Research subject summary

  • IL-19の免疫学的役割

  • 免疫系細胞におけるカルシウムシグナリングの役割解明

  • MASH/MAFLD発症機構の解明

  • 消化管と肝臓間の臓器連関機構の解明

  • IBD発症機構の解明

Research Career

  • The immunological role of interleukin-19

    Individual

    1992.10 - Now 

Job Career (off-campus)

  • 大阪公立大学大学院獣医学研究科教授

    2022.04 - Now

  • 大阪府立大学大学院生命環境科学研究科教授

    2021.04 - 2022.03

Papers

  • Deficiency of interleukin-19 exacerbates acute lung injury induced by intratracheal treatment of hydrochloric acid

    Kazuhiro Nishiyama, Joji Horikoshi, Toko Maehara, Miyuu Tanaka, Takashi Tanida, Koichi Kawada, Susumu Takeshita, Naoshige Ono, Takeshi Izawa, Mitsuru Kuwamura, Yasu Taka Azuma

    Journal of Pharmacological Sciences   155 ( 3 )   94 - 100   2024.07( ISSN:1347-8613 ( eISSN:1347-8648

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    Publishing type:Research paper (scientific journal)  

    Interleukin (IL-19) belongs to the IL-10 family of cytokines and plays diverse roles in inflammation, cell development, viral responses, and lipid metabolism. Acute lung injury (ALI) is a severe respiratory condition associated with various diseases, including severe pneumonia, sepsis, and trauma, lacking established treatments. However, the role of IL-19 in acute inflammation of the lungs is unknown. We reported the impact of IL-19 functional deficiency in mice crossed with an ALI model using HCl. Lungs damages, neutrophil infiltration, and pulmonary edema induced by HCl were significantly worse in IL-19 knockout (KO) mice than in wild-type (WT) mice. mRNA expression levels of C-X-C motif chemokine ligand 1 (CXCL1) and IL-6 in the lungs were significantly higher in IL-19 KO mice than in WT mice. Little apoptosis was detected in lung injury in WT mice, whereas apoptosis was observed in exacerbated area of lung injury in IL-19 KO mice. These results are the first to show that IL-19 is involved in acute inflammation of the lungs, suggesting a novel molecular mechanism in acute respiratory failures. If it can be shown that neutrophils have IL-19 receptors and that IL-19 acts directly on them, it would be a novel drug target.

    DOI: 10.1016/j.jphs.2024.04.003

    PubMed

  • Inhibition of Drp1-Filamin Protein Complex Prevents Hepatic Lipid Droplet Accumulation by Increasing Mitochondria-Lipid Droplet Contact.

    Kohei Ariyoshi, Kazuhiro Nishiyama, Yuri Kato, Xinya Mi, Tomoya Ito, Yasu-Taka Azuma, Akiyuki Nishimura, Motohiro Nishida

    International journal of molecular sciences   25 ( 10 )   2024.05

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:International journal  

    Lipid droplet (LD) accumulation in hepatocytes is one of the major symptoms associated with fatty liver disease. Mitochondria play a key role in catabolizing fatty acids for energy production through β-oxidation. The interplay between mitochondria and LD assumes a crucial role in lipid metabolism, while it is obscure how mitochondrial morphology affects systemic lipid metabolism in the liver. We previously reported that cilnidipine, an already existing anti-hypertensive drug, can prevent pathological mitochondrial fission by inhibiting protein-protein interaction between dynamin-related protein 1 (Drp1) and filamin, an actin-binding protein. Here, we found that cilnidipine and its new dihydropyridine (DHP) derivative, 1,4-DHP, which lacks Ca2+ channel-blocking action of cilnidipine, prevent the palmitic acid-induced Drp1-filamin interaction, LD accumulation and cytotoxicity of human hepatic HepG2 cells. Cilnidipine and 1,4-DHP also suppressed the LD accumulation accompanied by reducing mitochondrial contact with LD in obese model and high-fat diet-fed mouse livers. These results propose that targeting the Drp1-filamin interaction become a new strategy for the prevention or treatment of fatty liver disease.

    DOI: 10.3390/ijms25105446

    PubMed

  • Pharmacological Activation of TRPC6 Channel Prevents Colitis Progression.

    Kazuhiro Nishiyama, Yuri Kato, Akiyuki Nishimura, Xinya Mi, Ryu Nagata, Yasuo Mori, Yasu-Taka Azuma, Motohiro Nishida

    International journal of molecular sciences   25 ( 4 )   2024.02

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:International journal  

    We recently reported that transient receptor potential canonical (TRPC) 6 channel activity contributes to intracellular Zn2+ homeostasis in the heart. Zn2+ has also been implicated in the regulation of intestinal redox and microbial homeostasis. This study aims to investigate the role of TRPC6-mediated Zn2+ influx in the stress resistance of the intestine. The expression profile of TRPC1-C7 mRNAs in the actively inflamed mucosa from inflammatory bowel disease (IBD) patients was analyzed using the GEO database. Systemic TRPC3 knockout (KO) and TRPC6 KO mice were treated with dextran sulfate sodium (DSS) to induce colitis. The Zn2+ concentration and the mRNA expression levels of oxidative/inflammatory markers in colon tissues were quantitatively analyzed, and gut microbiota profiles were compared. TRPC6 mRNA expression level was increased in IBD patients and DSS-treated mouse colon tissues. DSS-treated TRPC6 KO mice, but not TRPC3 KO mice, showed severe weight loss and increased disease activity index compared with DSS-treated WT mice. The mRNA abundances of antioxidant proteins were basically increased in the TRPC6 KO colon, with changes in gut microbiota profiles. Treatment with TRPC6 activator prevented the DSS-induced colitis progression accompanied by increasing Zn2+ concentration. We suggest that TRPC6-mediated Zn2+ influx activity plays a key role in stress resistance against IBD, providing a new strategy for treating colitis.

    DOI: 10.3390/ijms25042401

    PubMed

  • Functional role of IL-19 in a mouse model of L-arginine-induced pancreatitis and related lung injury.

    Naoshige Ono, Joji Horikoshi, Takeshi Izawa, Kazuhiro Nishiyama, Miyuu Tanaka, Takashi Fujita, Mitsuru Kuwamura, Yasu-Taka Azuma

    Experimental animals   73 ( 2 )   175 - 185   2023.12( ISSN:0007-5124

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:Domestic journal  

    IL-19 is a member of IL-10 family and is mainly produced by macrophages. Acute pancreatitis (AP) is an inflammatory disease characterized by acinar cell injury and necrosis. In the present study, the role of IL-19 in AP and AP-associated lung injury in mice was explored using L-arginine-induced pancreatitis. Experimental pancreatitis was induced by intraperitoneal injection of L-arginine in wild-type (WT) and IL-19 gene deficient (IL-19 KO) mice. In L-arginine treated mice, the serum amylase level was significantly increased in IL-19 KO mice, and interstitial edema, analyzed using hematoxylin and eosin (H&E)-stained sections, was aggravated mildly in IL-19 KO mice compared to WT mice. Compared to WT mice treated with L-arginine, mRNA expression of tumor necrosis factor (TNF)-α was significantly upregulated in IL-19 KO mice treated with L-arginine. In WT mice, IL-19 mRNA was equally expressed in the pancreas of both control and L-arginine treated mice. The condition of lung alveoli in WT and IL-19 KO mice treated with L-arginine was then evaluated. In mice with L-arginine-induced pancreatitis, alveolar area was remarkedly decreased, and expression of lung myeloperoxidase was significantly increased in IL-19 KO mice compared to WT mice. In the lungs, mRNA expressions of IL-6 and inducible nitric oxide synthase were significantly increased in IL-19 KO mice compared to WT mice. In summary, IL-19 was proposed to alleviate L-arginine-induced pancreatitis by regulating TNF-α production and to protect against AP-related lung injury by inhibiting neutrophil migration.

    DOI: 10.1538/expanim.23-0094

    PubMed

  • Interleukin-19 Gene-Deficient Mice Promote Liver Fibrosis via Enhanced TGF-β Signaling, and the Interleukin-19-CCL2 Axis Is Important in the Direction of Liver Fibrosis.

    Naoshige Ono, Takashi Fujita, Mariko Miki, Kazuhiro Nishiyama, Takeshi Izawa, Tomoko Aoyama, Mitsuru Kuwamura, Hideki Fujii, Yasu-Taka Azuma

    Biomedicines   11 ( 7 )   2023.07( ISSN:2227-9059

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:International journal  

    IL-19 is a cytokine discovered by homologous searching with IL-10 and is produced by non-immune cells, such as keratinocytes, in addition to immune cells, such as macrophages. Liver fibrosis results from the inflammation and activation of hepatic stellate cells via chronic liver injury. However, the participation of IL-19 in liver fibrosis remains to be sufficiently elucidated. Our group studied the immunological function of IL-19 in a mouse model of carbon tetrachloride (CCl4)-induced liver fibrosis. IL-19 gene-deficient (KO) mice and body weight-matched wild-type (WT) mice were used. A liver fibrosis mouse model was created via CCl4 administration (two times per week) for 8 weeks. In CCl4-induced liver fibrosis, serum analysis revealed that IL-19 KO mice had higher ALT levels compared to WT mice. IL-19 KO mice had worse fibrosis, as assessed by morphological evaluation of total area stained positive with Azan and Masson trichrome. In addition, the expression of α-SMA was increased in liver tissues of IL-19 KO mice compared to WT mice. Furthermore, mRNA expression levels of TGF-β and α-SMA were enhanced in IL-19 KO mice compared to WT mice. In vitro assays revealed that IL-19-high expressing RAW264.7 cells inhibited the migration of NIH3T3 cells via the inhibited expression of CCL2 in the presence of CCl4 and IL-4. These findings indicate that IL-19 plays a critical role in liver fibrosis by affecting TGF-β signaling and the migration of hepatic stellate cells during liver injury. Enhancement of the IL-19 signaling pathway is a potential treatment for liver fibrosis.

    DOI: 10.3390/biomedicines11072064

    PubMed

  • L-arginine-induced pancreatitis aggravated by inhibiting Na+/Ca2+ exchanger 1.

    Naoshige Ono, Joji Horikoshi, Takeshi Izawa, Kazuhiro Nishiyama, Miyuu Tanaka, Mitsuru Kuwamura, Yasu-Taka Azuma

    The Journal of veterinary medical science   85 ( 6 )   657 - 666   2023.04( ISSN:0916-7250

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:Domestic journal  

    Na+/Ca2+ exchangers (NCX) are an exchange transporter of Na+ and Ca2+ ions on the plasma membrane. There are three types of NCX: NCX1, NCX2, and NCX3. We have been working for many years to understand the role of NCX1 and NCX2 in gastrointestinal motility. In this study, we focused on the pancreas, an organ closely related to the gastrointestinal tract, and used a mouse model of acute pancreatitis to investigate a possible role for NCX1 in the pathogenesis of pancreatitis. We characterized a model of acute pancreatitis induced by excessive doses of L-arginine. We administered the NCX1 inhibitor SEA0400 (1 mg/kg) 1 hr prior to L-arginine-induced pancreatitis and evaluated pathological changes. Mice treated with NCX1 inhibitors show exacerbation of the disease with decreased survival and increased amylase activity in response to L-arginine-induced experimental acute pancreatitis, and this exacerbation correlates with increased autophagy mediated by LC3B and p62. These results suggest that NCX1 has a role in regulating pancreatic inflammation and acinar cell homeostasis.

    DOI: 10.1292/jvms.22-0569

    PubMed

  • Stress decreases contraction of the colon, and the effects of stress are different among the regions of the colon.

    Ono N, Suzuki S, Kawada K, Yamaguchi T, Azuma YT

    The Journal of veterinary medical science   84 ( 8 )   1061 - 1064   2022.08( ISSN:0916-7250

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  • Redox-dependent internalization of the purinergic P2Y6 receptor limits colitis progression.

    Kazuhiro Nishiyama, Akiyuki Nishimura, Kakeru Shimoda, Tomohiro Tanaka, Yuri Kato, Takahiro Shibata, Hiroshi Tanaka, Hitoshi Kurose, Yasu-Taka Azuma, Hideshi Ihara, Yoshito Kumagai, Takaaki Akaike, Philip Eaton, Koji Uchida, Motohiro Nishida

    Science signaling   15 ( 716 )   eabj0644   2022.01

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:International journal  

    After ligand stimulation, many G protein–coupled receptors (GPCRs) undergo β-arrestin–dependent desensitization, during which they are internalized and either degraded or recycled to the plasma membrane. Some GPCRs are not subject to this type of desensitization because they lack the residues required to interact with β-arrestins. We identified a mechanism of redox-dependent alternative internalization (REDAI) that promotes the internalization and degradation of the purinergic P2Y6 receptor (P2Y6R). Synthetic and natural compounds containing electrophilic isothiocyanate groups covalently modified P2Y6R at Cys220, which promoted the ubiquitylation of Lys137 and receptor internalization and degradation in various mouse and human cultured cell lines. Endogenous electrophiles also promoted ligand-dependent P2Y6R internalization and degradation. P2Y6R is highly abundant in inflammatory cells and promotes the pathogenesis of colitis. Deficiency in P2Y6R protected mice against experimentally induced colitis, and mice expressing a form of P2Y6R in which Cys220 was mutated to nonmodifiable serine were more sensitive to the induction of colitis. Several other GPCRs, including A2BAR, contain cysteine and lysine residues at the appropriate positions to mediate REDAI, and isothiocyanate stimulated the internalization of A2BAR and of a form of P2Y2R with insertions of the appropriate residues. Thus, endogenous and exogenous electrophiles may limit colitis progression through cysteine modification of P2Y6R and may also mediate internalization of other GPCRs.

    DOI: 10.1126/scisignal.abj0644

    PubMed

  • Recent topics on interorgan communication networks and gut microbiota

    Ono Naoshige, Azuma Yasu-Taka

    Folia Pharmacologica Japonica   157 ( 5 )   321 - 324   2022( ISSN:00155691 ( eISSN:13478397

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    <p>The living body is composed of diverse organ systems, each of which has its own characteristic control mechanisms and complex in vivo responses. Between the brain and organs such as the heart, kidney, liver, pancreas, gastrointestinal tract, and even muscles, there is a sophisticated and complex regulatory system. Coordinated interactions through communication between organs are essential for maintaining health. In this review, we introduce four research trends in inter-organ networks, with a focus on the digestive system: 1) Inter-organ networks on metabolic systems, 2) Inter-organ networks originating from the gastrointestinal tract, 3) Intestinal bacteria, that is one of the biggest topics in recent years, 4) Research results on the involvement of gut microbiota in the inter-organ network between the kidney and the gastrointestinal tract. An integrated understanding and investigation of the regulatory mechanisms of inter-organ communication networks are expected to extend healthy life span and improve quality of life.</p>

    DOI: 10.1254/fpj.22038

    PubMed

  • IL-19 Contributes to the Development of Nonalcoholic Steatohepatitis by Altering Lipid Metabolism.

    Yasu-Taka Azuma, Takashi Fujita, Takeshi Izawa, Kana Hirota, Kazuhiro Nishiyama, Airi Ikegami, Tomoko Aoyama, Mikihito Ike, Yumi Ushikai, Mitsuru Kuwamura, Hideki Fujii, Koichi Tsuneyama

    Cells   10 ( 12 )   2021.12

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:International journal  

    Interleukin (IL)-19, a member of the IL-10 family, is an anti-inflammatory cytokine produced primarily by macrophages. Nonalcoholic steatohepatitis (NASH) is a disease that has progressed from nonalcoholic fatty liver disease (NAFLD) and is characterized by inflammation and fibrosis. We evaluated the functions of IL-19 in a NAFLD/NASH mouse model using a 60% high fat diet with 0.1% methionine, without choline, and with 2% cholesterol (CDAHFD). Wild-type (WT) and IL-19 gene-deficient (KO) mice were fed a CDAHFD or standard diet for 9 weeks. Liver injury, inflammation, and fibrosis induced by CDAHFD were significantly worse in IL-19 KO mice than in WT mice. IL-6, TNF-α, and TGF-β were significantly higher in IL-19 KO mice than in WT mice. As a mechanism using an in vitro experiment, palmitate-induced triglyceride and cholesterol contents were decreased by the addition of IL-19 in HepG2 cells. Furthermore, addition of IL-19 decreased the expression of fatty acid synthesis-related enzymes and increased ATP content in HepG2 cells. The action of IL-19 in vitro suppressed lipid metabolism. In conclusion, IL-19 may play an important role in the development of steatosis and fibrosis by directly regulating liver metabolism and may be a potential target for the treatment of liver diseases.

    DOI: 10.3390/cells10123513

    PubMed

  • IL-19の抗炎症作用を活かした治療への応用 Reviewed

    小野尚重,東 泰孝

    日本薬理学雑誌 雑誌   156 ( 5 )   288 - 291   2021.05

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    Kind of work:Joint Work  

  • Gastrointestinal motility modulation by stress is associated with reduced smooth muscle contraction through specific transient receptor potential channel.

    Yasu-Taka Azuma, Sho Suzuki, Kazuhiro Nishiyama, Taro Yamaguchi

    The Journal of veterinary medical science   2021.02

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:Domestic journal  

    Excessive stress response causes disability in social life. There are many diseases caused by stress, such as gastrointestinal motility disorders, depression, eating disorders, and cardiovascular diseases. Transient receptor potential (TRP) channels underlie non-selective cation currents and are downstream effectors of G protein-coupled receptors. Ca2+ influx is important for smooth muscle contraction, which is responsible for gastrointestinal motility. Little is known about the possible involvement of TRP channels in the gastrointestinal motility disorders due to stress. The purpose of this study was to measure the changes in gastrointestinal motility caused by stress and to elucidate the mechanism of these changes. The stress model used the water immersion restraint stress. Gastrointestinal motility, especially the ileum, was recorded responses to electric field stimulation (EFS) by isometric transducer. EFS-induced contraction was significantly reduced in the ileum of stressed mouse. Even under the conditions treated with atropine, EFS-induced contraction was significantly reduced in the ileum of stressed mouse. In addition, carbachol-induced, neurokinin A-induced, and substance P-induced contractions were all significantly reduced in the ileum of stressed mouse. Furthermore, the expression of TRPC3 was decreased in the ileum of stressed mouse. These results suggest that the gastrointestinal motility disorders due to stress is associated with specific non-selective cation channel.

    DOI: 10.1292/jvms.20-0490

    PubMed

  • Interleukin-19 as an immunoregulatory cytokine. Reviewed

    Fujimoto Y, Kuramoto N, Yoneyama M, Azuma YT.

    Curr. Mol. Pharmacol. 雑誌   14 ( 2 )   191 - 199   2021.02

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    Kind of work:Joint Work  

  • Interleukin-19 abrogates experimental autoimmune encephalomyelitis by attenuating antigen-presenting cell activation. Reviewed

    Horiuchi H, Parajuli B, Komiya H, Ogawa Y, Jin S, Takahashi K, Azuma YT, Tanaka F, Suzumura A, Takeuchi H.

    Front. Immunol. 雑誌   12   2021

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    Kind of work:Joint Work  

  • Ablation of interleukin-19 improves motor function in a mouse model of amyotrophic lateral sclerosis. Reviewed

    Komiya H, Takeuchi H, Ogawa Y, Suzuki K, Ogasawara A, Takahashi K, Azuma YT, Doi H, Tanaka F.

    Molecular Brain 雑誌   14 ( 1 )   2021

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    Kind of work:Joint Work  

  • Deficiency of interleukin-19 exacerbates lipopolysaccharide/D-galactosamine-induced acute liver failure. Reviewed

    Fujimoto Y, Kuwamura M, Azuma YT.

    J. Vet. Med. Sci. 雑誌   82 ( 10 )   1450 - 1455   2020.10

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    Kind of work:Joint Work  

  • Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes-7. Reviewed

    Gütschow M, Vanden Eynde JJ, Jampílek J, Kang CB, Mangoni AA, Fossa P, Karaman R, Trabocchi A, Scott PJH, Reynisson J, Rapposelli S, Galdiero S, Winum JY, Brullo C, Prokai-Tatrai K, Sharma AK, Schapira M, Azuma YT, Cerchia L, Spetea M, Torri G, Collina S, Geronikaki A, García-Sosa AT, Vasconcelos MH, Sousa ME, Kosalec I, Tuccinardi T, Duarte IF, Salvador JAR, Bertinaria M, Pellecchia M, Amato J, Rastelli G, Gomes PAC, Guedes RC, Sabatier JM, Estévez-Braun A, Pagano B, Mangani S, Ragno R, Kokotos G, Brindisi M, González FV, Borges F, Miloso M, Rautio J, Muñoz-Torrero D.

    Molecules 雑誌   2020.07

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    Kind of work:Joint Work  

  • Interleukin-19 enhances cytokine production induced by lipopolysaccharide and inhibits cytokine production induced by polyI:C in BALB/c mice. Reviewed

    Yasu-Taka Azuma, Kazuhiro Nishiyama

    The Journal of veterinary medical science   2020.05

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    Authorship:Corresponding author   International / domestic magazine:Domestic journal  

    Interleukin (IL)-19 is a cytokine of the IL-10 family. There are many reports on the involvement of IL-19 in several human diseases. There also are many reports elucidating the role of IL-19 using mouse disease models. Most reports use C57BL/6 mice, whereas few reports use BALB/c mice, in terms of the mouse disease model that the researchers used in the present study. To date, research on the role of IL-19 is diversified, yet some basic mechanisms are still unclear. In this study, we administered lipopolysaccharide (LPS), polyI:C, and CpG to BALB/c mice, measured more than 20 cytokines in the blood and compared them with that of the wild-type and IL-19-deficient (IL-19 KO) mice. LPS is associated with bacterial infection, polyI:C is associated with viral infection, and CpG is associated with both bacterial and viral infections. Among the cytokines measured, the results of experiments using LPS revealed that the production of some cytokines was suppressed in IL-19 KO mice. Interestingly, the experiments using polyI:C revealed that production of some cytokines was enhanced in IL-19 KO mice. However, the experiments using CpG have shown that the production of only one cytokine was enhanced in IL-19 KO mice. These results revealed that cytokine production in the blood was regulated by IL-19, and the type of regulation was dependent on the administered stimulant.

    DOI: 10.1292/jvms.20-0137

    PubMed

  • Interleukin-19 as an immunoregulatory cytokine

    Yasuyuki Fujimoto, Nobuyuki Kuramoto, Masanori Yoneyama, Yasu-Taka Azuma

    Current Molecular Pharmacology   13   2020.04( ISSN:1874-4672

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    Publishing type:Research paper (scientific journal)  

    <sec>
    <title>:</title>
    IL-19 is a type of anti-inflammatory cytokine. Since the receptor for IL-19 is common
    to IL-20 and IL-24, it is important to clarify the role of each of the three. If three
    different cytokines bind to the same receptor, these three may have been produced to
    complement the other two. However perhaps it is unlikely. Recently, the existence of a
    novel receptor for IL-19 was suggested. The distinction between the three roles still
    makes sense. On the other hand, because T cells do not produce IL-19, their role in
    acquired immunity is limited or indirect. It has been reported that IL-19 causes
    inflammation in some diseases but is not an anti-inflammatory effect. In this review, we
    introduce the current role of IL-19 in each disease. In addition, we will describe the
    molecular mechanism of IL-19 and its development for prevention. IL-19 was
    previously considered an anti-inflammatory cytokine, but we would like to propose
    what we call an immunoregulatory cytokine.



    </sec>

    DOI: 10.2174/1874467213666200424151528

  • Fucoxanthin Ameliorates Atopic Dermatitis Symptoms by Regulating Keratinocytes and Regulatory Innate Lymphoid Cells Reviewed

    Chika Natsume, Nao Aoki, Tomoko Aoyama, Keisuke Senda, Mio Matsui, Airi Ikegami, Kosuke Tanaka, Yasu-Taka Azuma, Takashi Fujita

    International Journal of Molecular Sciences   21 ( 6 )   2180 - 2180   2020.03( eISSN:1422-0067

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    Publishing type:Research paper (scientific journal)  

    Fucoxanthin (FX) is a xanthophyll that is contained abundantly in marine plants. The biological action of FX includes its antioxidant and anti-lipogenic activities, while the precise action of its mechanisms on skin cells has not yet been clarified. The current study examined the effect of FX in comparison with tacrolimus (TAC) on NC/Nga mice, which are an atopic dermatitis (AD) model. FX topical treatment dramatically ameliorated itching behavior over the TAC treatment, which was insufficient for improvement of AD symptoms. In Nc/Nga mice, FX or TAC applied to the skin inhibited eosinophil infiltration with decreased expression of Il-33. FX also stimulated Il-2, Il-5, Il-13, Il-10, and TGF-β expression levels, and Sca1+Il-10+TGF-β+ regulatory innate lymphoid cells (ILCreg) were dominantly observed in FX treated skin epidermal keratinocytes and dermal layers. This combined evidence demonstrated that FX exerts anti-inflammatory effects on keratinocytes and ameliorates AD symptoms by regulating ILCreg to normalize immune responses in an atopic dermatitis model.

    DOI: 10.3390/ijms21062180

  • Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes-6. Reviewed

    Vanden Eynde JJ, Mangoni AA, Rautio J, Leprince J, Azuma YT, García-Sosa AT, Hulme C, Jampilek J, Karaman R, Li W, Gomes PAC, Hadjipavlou-Litina D, Capasso R, Geronikaki A, Cerchia L, Sabatier JM, Ragno R, Tuccinardi T, Trabocchi A, Winum JY, Luque FJ, Prokai-Tatrai K, Spetea M, Gütschow M, Kosalec I, Guillou C, Vasconcelos MH, Kokotos G, Rastelli G, de Sousa ME, Manera C, Gemma S, Mangani S, Siciliano C, Galdiero S, Liu H, Scott PJH, de Los Ríos C, Agrofoglio LA, Collina S, Guedes RC, Muñoz-Torrero D.

    Molecules 雑誌   2020.01

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    Kind of work:Joint Work  

  • Fucoxanthin ameliorates atopic dermatitis symptoms by regulating keratinocytes and regulatory innate lymphoid cells. Reviewed

    Natsume C, Aoki N, Aoyama T, Senda K, Matsui M, Ikegami A, Tanaka K, Azuma YT, Fujita T.

    Int J Mol Sci 雑誌   2020

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    Kind of work:Joint Work  

  • Interleukin-19 enhances cytokine production induced by lipopolysaccharide and inhibits cytokine production induced by polyI:C in BALB/c mice. Reviewed

    Azuma YT, Nishiyama K.

    J Vet Med Sci 雑誌   2020

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    Kind of work:Joint Work  

  • Deficiency of interleukin-19 exacerbates lipopolysaccharide/D-galactosamine-induced acute liver failure Reviewed

    Yasuyuki FUJIMOTO, Mitsuru KUWAMURA, Yasu-Taka AZUMA

    Journal of Veterinary Medical Science   82 ( 10 )   1450 - 1455   2020( ISSN:0916-7250 ( eISSN:1347-7439

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    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)  

    DOI: 10.1292/jvms.20-0344

  • Ibudilast attenuates doxorubicin-induced cytotoxicity by suppressing formation of TRPC3 channel and NADPH oxidase 2 protein complexes. Reviewed

    Kazuhiro Nishiyama, Takuro Numaga-Tomita, Yasuyuki Fujimoto, Tomohiro Tanaka, Chiemi Toyama, Akiyuki Nishimura, Tomohiro Yamashita, Naoya Matsunaga, Satoru Koyanagi, Yasu-Taka Azuma, Yuko Ibuki, Koji Uchida, Shigehiro Ohdo, Motohiro Nishida

    British journal of pharmacology   176 ( 18 )   3723 - 3738   2019.09( ISSN:0007-1188

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    Publishing type:Research paper (scientific journal)   International / domestic magazine:International journal  

    BACKGROUND AND PURPOSE: Doxorubicin is a highly effective anticancer agent but eventually induces cardiotoxicity associated with increased production of ROS. We previously reported that a pathological protein interaction between TRPC3 channels and NADPH oxidase 2 (Nox2) contributed to doxorubicin-induced cardiac atrophy in mice. Here we have investigated the effects of ibudilast, a drug already approved for clinical use and known to block doxorubicin-induced cytotoxicity, on the TRPC3-Nox2 complex. We specifically sought evidence that this drug attenuated doxorubicin-induced systemic tissue wasting in mice. EXPERIMENTAL APPROACH: We used the RAW264.7 macrophage cell line to screen 1,271 clinically approved chemical compounds, evaluating functional interactions between TRPC3 channels and Nox2, by measuring Nox2 protein stability and ROS production, with and without exposure to doxorubicin. In male C57BL/6 mice, samples of cardiac and gastrocnemius muscle were taken and analysed with morphometric, immunohistochemical, RT-PCR and western blot methods. In the passive smoking model, cells were exposed to DMEM containing cigarette sidestream smoke. KEY RESULTS: Ibudilast, an anti-asthmatic drug, attenuated ROS-mediated muscle toxicity induced by doxorubicin treatment or passive smoking, by inhibiting the functional interactions between TRPC3 channels and Nox2, without reducing TRPC3 channel activity. CONCLUSIONS AND IMPLICATIONS: These results indicate a common mechanism underlying induction of systemic tissue wasting by doxorubicin. They also suggest that ibudilast could be repurposed to prevent muscle toxicity caused by anticancer drugs or passive smoking.

    DOI: 10.1111/bph.14777

    PubMed

  • Chronic kidney disease after 5/6 nephrectomy disturbs the intestinal microbiota and alters intestinal motility. Reviewed

    Kazuhiro Nishiyama, Kimiya Aono, Yasuyuki Fujimoto, Mitsuru Kuwamura, Toshiya Okada, Hayato Tokumoto, Takeshi Izawa, Ryoichi Okano, Hidemitsu Nakajima, Tadayoshi Takeuchi, Yasu-Taka Azuma

    Journal of cellular physiology   234 ( 5 )   6667 - 6678   2019.05( ISSN:0021-9541

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    International / domestic magazine:International journal  

    Organ-organ crosstalk is involved in homeostasis. Gastrointestinal symptoms are common in patients with renal failure. The aim of this study was to elucidate the relationship between gastrointestinal motility and gastrointestinal symptoms in chronic kidney disease. We performed studies in C57BL/6 mice with chronic kidney disease after 5/6 nephrectomy. Gastrointestinal motility was evaluated by assessing the ex vivo responses of ileum and distal colon strips to electrical field stimulation. Feces were collected from mice, and the composition of the gut microbiota was analyzed using 16S ribosomal RNA sequencing. Mice with chronic kidney disease after 5/6 nephrectomy showed a decreased amount of stool, and this constipation was correlated with a suppressed contraction response in ileum motility and decreased relaxation response in distal colon motility. Spermine, one of the uremic toxins, inhibited the contraction response in ileum motility, but four types of uremic toxins showed no effect on the relaxation response in distal colon motility. The 5/6 nephrectomy procedure disturbed the balance of the gut microbiota in the mice. The motility dysregulation and constipation were resolved by antibiotic treatments. The expression levels of interleukin 6, tumor necrosis factor-α, and iNOS in 5/6 nephrectomy mice were increased in the distal colon but not in the ileum. In addition, macrophage infiltration in 5/6 nephrectomy mice was increased in the distal colon but not in the ileum. We found that 5/6 nephrectomy altered gastrointestinal motility and caused constipation by changing the gut microbiota and causing colonic inflammation. These findings indicate that renal failure was remarkably associated with gastrointestinal dysregulation.

    DOI: 10.1002/jcp.27408

    PubMed

  • Correlation between toll-like receptor 4 and nucleotide-binding oligomerization domain 2 (NOD2) and pathological severity in dogs with chronic gastrointestinal diseases. Reviewed

    Kimiya Aono, Yasu-Taka Azuma, Tomoyo Nabetani, Shingo Hatoya, Masaru Furuya, Mariko Miki, Kana Hirota, Yasuyuki Fujimoto, Kazuhiro Nishiyama, Yoshiyuki Ogata, Tomofumi Mochizuki, Hiroyuki Tani

    Veterinary immunology and immunopathology   210   15 - 22   2019.04( ISSN:0165-2427

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    International / domestic magazine:International journal  

    Toll-like receptor 4 (TLR4), nucleotide-binding oligomerization domain 2 (NOD2), and TNF-α play important roles in human inflammatory bowel diseases. The aim of this study was to elucidate the relationship between Toll-like receptor 4, NOD2, and TNF-α and the severity of chronic gastrointestinal diseases in dogs. We examined the expression levels of TLR4, NOD2, and TNF-α in the stomach, duodenum, ileum, colon, and rectum obtained from 21 dogs with chronic gastrointestinal disease, including inflammatory bowel disease, high-grade lymphoma, food responsive enteropathy, chronic pancreatitis, low-grade lymphoma, inflammatory colorectal polyp, and chronic colitis. Next, we demonstrated whether there is good correlation between the expression levels of TLR4, NOD2, and TNF-α and the histopathological analysis of each sample. We found that the level of TLR4 expression in the ileum of dogs with chronic gastrointestinal disease was positively associated with the histopathological severity. We also found that the level of NOD2 expression in the duodenum, stomach, and rectum was positively associated with the histopathological severity. However, there was no correlation between TNF-α expression in the 5 regions tested in this study and the histopathological severity. These findings indicate that TLR4 and NOD2 are remarkably associated with the severity of chronic gastrointestinal disease in dogs.

    DOI: 10.1016/j.vetimm.2019.03.003

    PubMed

  • Chronic kidney disease following 5/6 nephrectomy disturbs the intestinal microbiota and alters intestinal motility. Reviewed

    Nishiyama K, Aono K, Fujimoto Y, Kuwamura M, Okada T, Tokumoto H, Izawa T, Okano R, Nakajima H, Takeuchi T, Azuma YT.

    J Cell Physiol 雑誌   234 ( 5 )   6667 - 6678   2019

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    Kind of work:Joint Work  

  • Ibudilast attenuates doxorubicin-induced cytotoxicity by suppressing formation of TRPC3-Nox2 protein complex. Reviewed

    Nishiyama K, Numaga-Tomita T, Fujimoto Y, Tanaka T, Toyama C, Nishimura A, Yamashita T, Matsunaga N, Koyanagi S, Azuma YT, Ibuki Y, Uchida K, Ohdo S, Nishida M.

    Br J Pharmacol 雑誌   2019

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    Kind of work:Joint Work  

  • Correlation between toll-like receptor 4 and nucleotide-binding oligomerization domain 2 (NOD2) and pathological severity in dogs with chronic gastrointestinal diseases. Reviewed

    Aono K, Azuma YT, Nabetani T, Hatoya S, Furuya M, Miki M, Hirota K, Fujimoto Y, Nishiyama K, Ogata Y, Mochizuki T, Tani H.

    Veterinary Immunology and Immunopathology 雑誌   210   15 - 22   2019

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    Kind of work:Joint Work  

  • Fatty acid transport protein 1 enhances the macrophage inflammatory response by coupling with ceramide and c-Jun N-terminal kinase signaling. Reviewed

    Nishiyama K, Fujita T, Fujimoto Y, Nakajima H, Takeuchi T, Azuma YT.

    Int Immunopharmacol 雑誌   55   205 - 215   2018

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    Kind of work:Joint Work  

  • Lauric acid alleviates neuroinflammatory responses by activated microglia: involvement of the GPR40-dependent pathway. Reviewed

    Nishimura Y, Moriyama M, Kawabe K, Satoh H, Takano K, Azuma YT, Nakamura Y.

    Neurochemical Research 雑誌   43 ( 9 )   723 - 1735   2018

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    Kind of work:Joint Work  

  • The Role of Interleukin-19 in Contact Hypersensitivity. Reviewed

    Fujimoto Y, Fujita T, Kuramoto N, Kuwamura M, Izawa T, Nishiyama K, Yoshida N, Nakajima H, Takeuchi T, Azuma YT.

    Biol Pharma Bull 雑誌   41 ( 2 )   182 - 189   2018

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    Kind of work:Joint Work  

  • Extracellular poly(ADP-ribose) is a neurotrophic signal that upregulates glial cell line-derived neurotrophic factor (GDNF) levels in vitro and in vivo. Reviewed

    4. Nakajima H, Itakura M, Sato K, Nakamura S, Azuma YT, Takeuchi T.

    Biochem Biophys Res Commun 雑誌   2017.03

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    Kind of work:Joint Work  

  • Na+/Ca2+ exchanger contribute to stool transport in mice with experimental diarrhea Reviewed

    Nishiyama K, Tanioka K, Azuma YT, Hayashi S, Fujimoto Y, Yoshida N, Kita S, Suzuki S, Nakajima H, Iwamoto T, Takeuchi T

    J Vet Med Sci 雑誌   2017.02

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    Kind of work:Joint Work  

  • Interleukin-19 is cardioprotective in dominant negative cyclic adenosine monophosphate response-element binding protein-mediated heart failure in a sex-specific manner. Reviewed

    Bruns DR, Ghincea AR, Ghincea CV, Azuma YT, Watson PA, Autieri MV, Walker LA.

    World J Cardiol 雑誌   9 ( 8 )   673 - 684   2017

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    Kind of work:Joint Work  

  • Exacerbated experimental pancreatitis in interleukin-19 knockout mice. Reviewed

    Fujimoto Y, Tsuneyama K, Kuramoto N, Hayashi S, Yoshida N, Morioka A, Teramoto M, Nakajima H, Takeuchi T, Azuma YT.

    Glob Drugs Therap 雑誌   2 ( 5 )   1 - 5   2017

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    Kind of work:Joint Work  

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MISC

  • Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes–7

    Michael Gütschow, Jean Jacques Vanden Eynde, Josef Jampilek, CongBao Kang, Arduino A. Mangoni, Paola Fossa, Rafik Karaman, Andrea Trabocchi, Peter J. H. Scott, Jóhannes Reynisson, Simona Rapposelli, Stefania Galdiero, Jean-Yves Winum, Chiara Brullo, Katalin Prokai-Tatrai, Arun K. Sharma, Matthieu Schapira, Yasu-Taka Azuma, Laura Cerchia, Mariana Spetea, Giangiacomo Torri, Simona Collina, Athina Geronikaki, Alfonso T. García-Sosa, M. Helena Vasconcelos, Maria Emília Sousa, Ivan Kosalec, Tiziano Tuccinardi, Iola F. Duarte, Jorge A. R. Salvador, Massimo Bertinaria, Maurizio Pellecchia, Jussara Amato, Giulio Rastelli, Paula A. C. Gomes, Rita C. Guedes, Jean-Marc Sabatier, Ana Estévez-Braun, Bruno Pagano, Stefano Mangani, Rino Ragno, George Kokotos, Margherita Brindisi, Florenci V. González, Fernanda Borges, Mariarosaria Miloso, Jarkko Rautio, Diego Muñoz-Torrero

    Molecules   25 ( 13 )   2968 - 2968   2020.06( eISSN:1420-3049

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    Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes is a series of editorials which is published on a biannual basis by the Editorial Board of the Medicinal Chemistry section of the journal Molecules [...]

    DOI: 10.3390/molecules25132968

  • Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes–6

    Jean Jacques Vanden Eynde, Arduino A. Mangoni, Jarkko Rautio, Jérôme Leprince, Yasu-Taka Azuma, Alfonso T. García-Sosa, Christopher Hulme, Josef Jampilek, Rafik Karaman, Wei Li, Paula A. C. Gomes, Dimitra Hadjipavlou-Litina, Raffaele Capasso, Athina Geronikaki, Laura Cerchia, Jean-Marc Sabatier, Rino Ragno, Tiziano Tuccinardi, Andrea Trabocchi, Jean-Yves Winum, F. Javier Luque, Katalin Prokai-Tatrai, Mariana Spetea, Michael Gütschow, Ivan Kosalec, Catherine Guillou, M. Helena Vasconcelos, George Kokotos, Giulio Rastelli, Maria Emília de Sousa, Clementina Manera, Sandra Gemma, Stefano Mangani, Carlo Siciliano, Stefania Galdiero, Hong Liu, Peter J. H. Scott, Cristóbal de los Ríos, Luigi A. Agrofoglio, Simona Collina, Rita C. Guedes, Diego Muñoz-Torrero

    Molecules   25 ( 1 )   119 - 119   2019.12( eISSN:1420-3049

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    Breakthroughs in Medicinal Chemistry: New Targets and Mechanisms, New Drugs, New Hopes is a series of Editorials that is published on a biannual basis by the Editorial Board of the Medicinal Chemistry section of the journal Molecules [...]

    DOI: 10.3390/molecules25010119

Presentations

  • 脂質代謝におけるインターロイキン-19の新規調節機構

    東 泰孝

    肝臓  2022.09  (一社)日本肝臓学会

  • 小腸消化管運動におけるストレス負荷に伴う収縮反応の抑制.

    東 泰孝、山口太郎

    第140回日本薬理学会近畿部会  2021.11 

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    Presentation type:Poster presentation  

  • インターロイキン-19は四塩化炭素による肝線維化形成に関与する. Domestic conference

    小野尚重、三木万梨子、東 泰孝

    第140回日本薬理学会近畿部会  2021.11 

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    Presentation type:Poster presentation  

  • Therapeutic application utilizing the anti-inflammatory effect of IL-19. Domestic conference

    東 泰孝

    第94回日本薬理学会年  2021.03 

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    Presentation type:Poster presentation  

Outline of collaborative research (seeds)

  • NASHモデルマウスを用いた治療作用点の解析

  • アレルギーモデルを用いた治療作用点の解析

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    遅発性アレルギーモデルである①DTHテスト、②接触性皮膚炎を用いた治療作用点の解析

  • IBDモデルマウスを用いた治療作用点の解析

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    IBDモデルマウスとして①DSS誘導性腸炎、②TNBS誘導性腸炎、③オキサゾロン誘導性腸炎)を用いた治療作用点の解析

Grant-in-Aid for Scientific Research

  • Elucidation of a novel regulatory mechanism by interleukin-19 in the pancreatic immune system

    Grant-in-Aid for Scientific Research(C)  2024

Charge of on-campus class subject

  • 獣医薬理学実習

    2024   Weekly class   Undergraduate

  • 獣医薬理学B

    2024   Weekly class   Undergraduate

  • 小動物基礎臨床実習

    2024   Intensive lecture   Undergraduate

  • 獣医学関連法規

    2024   Weekly class   Undergraduate

  • 獣医臨床薬理学

    2024   Weekly class   Undergraduate

  • 獣医薬理学A

    2024   Weekly class   Undergraduate

  • 生命環境科学概論

    2024   Intensive lecture   Undergraduate

  • 初年次ゼミナール

    2024   Weekly class   Graduate school

  • 国際・国内インターンシップ

    2024   Intensive lecture   Graduate school

  • 獣医科学特別演習2

    2024   Intensive lecture   Graduate school

  • 獣医科学特別研究1

    2024   Intensive lecture   Graduate school

  • 獣医科学特別演習1

    2024   Intensive lecture   Graduate school

  • 獣医科学演習

    2024   Intensive lecture   Graduate school

  • 病態機能学特論

    2024   Intensive lecture   Graduate school

  • 統合バイオ機能学特別講義B

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別講義

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別研究H

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別研究G

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別研究E

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別研究C

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別研究A

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別演習C

    2024   Intensive lecture   Graduate school

  • 動物構造機能学特別演習A

    2024   Intensive lecture   Graduate school

  • 創薬フィージビリティ研究実習

    2024   Intensive lecture   Undergraduate

  • 創薬学概論

    2024   Intensive lecture   Undergraduate

  • 獣医科学英語演習

    2024   Intensive lecture   Undergraduate

  • Veterinary Pharmacology B

    2021    

  • Laws and Regulations concerning Veterinary Science

    2021    

  • Veterinary Clinical Pharmacology

    2021    

  • Fundamental Experiments of Biology

    2021   Practical Training  

  • Practice in Veterinary Pharmacology

    2021   Practical Training  

  • Animal Physiology on Basic

    2021    

  • Veterinary Pharmacology B

    2021    

  • Veterinary Pharmacology B

    2021    

  • Veterinary Pharmacology A

    2021    

  • Biology B

    2021    

  • Basic clinical practices

    2021   Practical Training  

  • Veterinary English

    2021    

  • Special Lecture: Integrated Functional Biosciences B

    2021    

  • Practice in Feasibility Study on Drug Discovery

    2021   Practical Training  

  • Introduction to Drug Discovery and Development

    2021    

▼display all

Faculty development activities

  • 口演発表  2023

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    9月12日に開催された「大阪公立大学におけるFDのあり方について考える(2)」において、「複数の担当教員による成績評価のバラツキから学べること」の演題名にて発表を行った。

  • 成果報告  2022

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    「薬理学関連科目の成績評価に関する年次推移」の論文名にて、大阪公立大学「大学教育」第1巻に掲載した。

Number of instructed thesis, researches

  • 2023

    [Number of doctoral thesis reviews] (chief):

  • 2023

    [Number of instructed the Master's Program] (letter term):1

Job title

  • Job title within the department

    School of Veterinary Science Department of Veterinary Science 

    学科長  2022.04 - 2023.03

  • Job title within the department

    Graduate School of Veterinary Science Department of Veterinary Science 

    専攻長  2022.04 - 2023.03