病態モデル先端医学研究センター

yoshimura aya

  (吉村 文)

Profile Information

Affiliation
Education and Research Center of Animal Models for Human Diseases, Fujita Health University
Degree
博士(農学)(岩手大学大学院)

Researcher number
90466483
J-GLOBAL ID
201701001372319426
researchmap Member ID
7000019882

Education

 3

Papers

 31
  • 白水 貴大, 吉村 文, 坂田 美和, 熊本 海生航, 釘田 雅則, 八代 百合子, 鈴木 慶幸, 大畑 敬一, 秋江 靖樹, 山口 太美雄, 高橋 和男, 長尾 静子
    日本腎臓学会誌, 66(4) 657-657, Jun, 2024  
  • 白水 貴大, 吉村 文, 坂田 美和, 熊本 海生航, 釘田 雅則, 高橋 和男, 長尾 静子
    日本腎臓学会誌, 65(3) 317-317, May, 2023  
  • Hitomi Matsuno, Shoko Tsuchimine, Kazunori O'Hashi, Kazuhisa Sakai, Kotaro Hattori, Shinsuke Hidese, Shingo Nakajima, Shuichi Chiba, Aya Yoshimura, Noriko Fukuzato, Mayumi Kando, Megumi Tatsumi, Shintaro Ogawa, Noritaka Ichinohe, Hiroshi Kunugi, Kazuhiro Sohya
    Molecular psychiatry, May 26, 2022  Peer-reviewed
    Several lines of evidence suggest that stress induces the neurovascular dysfunction associated with increased blood-brain barrier (BBB) permeability, which could be an important pathology linking stress and psychiatric disorders, including major depressive disorder (MDD). However, the detailed mechanism resulting in BBB dysfunction associated in the pathophysiology of MDD still remains unclear. Herein, we demonstrate the role of vascular endothelial growth factor (VEGF), a key mediator of vascular angiogenesis and BBB permeability, in stress-induced BBB dysfunction and depressive-like behavior development. We implemented an animal model of depression, chronic restraint stress (RS) in BALB/c mice, and found that the BBB permeability was significantly increased in chronically stressed mice. Immunohistochemical and electron microscopic observations revealed that increased BBB permeability was associated with both paracellular and transcellular barrier alterations in the brain endothelial cells. Pharmacological inhibition of VEGF receptor 2 (VEGFR2) using a specific monoclonal antibody (DC101) prevented chronic RS-induced BBB permeability and anhedonic behavior. Considered together, these results indicate that VEGF/VEGFR2 plays a crucial role in the pathogenesis of depression by increasing the BBB permeability, and suggest that VEGFR2 inhibition could be a potential therapeutic strategy for the MDD subtype associated with BBB dysfunction.
  • Kyongtae T. Bae*(*Equally-Contributed First Authors), Kanako Kumamoto*, Aya Yoshimura*, Masanori Kugita, Shigeo Horie, Tamio Yamaguchi, Junu T. Bae, Shizuko Nagao
    Journal of Nephrology, Nov 10, 2021  Peer-reviewedLead author
  • MD Uga Naoko, MD PhD Watanabe Shunsuke, MD Yasui Toshihiro, MD PhD Hara Fujio, MD PhD Suzuki Tatsuya, PhD Nakatani Masashi, PhD Yoshimura Aya, PhD Kumamoto Kanako, MD PhD Tsuchida Kunihiro, PhD Nagao Shizuko, MD Tsuchiya Tomonori, MD Kondo Yasuhiro, MD Naoe Atsuki
    Fujita Medical Journal, 7(2) 41-49, 2021  Peer-reviewed
    <p>Objectives: Proximal stoma creation in neonates results in growth failure and distal intestinal atrophy. "Recycling stool" consists of stool injection from the proximal limb to the distal limb of a stoma. Because this method may prevent distal bowel atrophy and increase body weight, we investigated the effects of recycling stool upon distal intestinal mucosa by generating an ileostomy model in rats.</p><p>Methods: An ileostomy was created 5 cm proximal to the cecum in male Wistar/ST rats. Discharged stool or saline was injected into the distal limb, twice per day for 7 days. The intestinal adaptation was assessed by measuring the villus height and counting goblet cell number. Proliferation and apoptosis were analyzed by Ki67 and TUNEL immunostaining.</p><p>Results: The ratios of the height of the distal villi (D) to the that of proximal villi (P) were 0.97 (median [range] of D and P length: 421 [240–729] μm and 436 [294–638] μm, P<0.05) in the stool-injected group and 0.81 in the saline-injected group (442 [315–641] μm and 548 [236–776] μm, P<0.05). Compared with the saline-injected group, the stool-injected group showed elevated numbers of goblet cells (3.6 [2.0–7.6] vs. 4.9 [2.4–7.5] cells/100-μm villus length) and Ki67-positive cells (26.8% [13.8%–35.4%] vs. 40.1% [31.2%–45.7%]), along with a reduced number of apoptotic cells (5.0 [2.0–14.0] vs. 4.0 [1.0–9.0] cells/100-μm villus length).</p><p>Conclusions: Recycling stool prevented distal intestinal atrophy; this experimental design may facilitate further studies concerning alternative methods to prevent intestinal atrophy and growth failure.</p>

Misc.

 43

Research Projects

 11