Altered expression of COX-2 in subdivisions of the hippocampus during aging and in Alzheimer's disease: The Hisayama study

Kouhei Fujimi, Kazuhito Noda, Kensuke Sasaki, Yoshinobu Wakisaka, Yumihiro Tanizaki, Mitsuo Iida, Yutaka Kiyohara, Shigenobu Kanba, Toru Iwaki

研究成果: ジャーナルへの寄稿学術誌査読

38 被引用数 (Scopus)

抄録

Background: It has been reported that nonsteroidal anti-inflammatory drugs may delay the onset of Alzheimer's disease (AD). Since nonsteroidal anti-inflammatory drugs inhibit cyclooxygenase (COX), COX-2, an inducible form of COX, may be involved in the pathology of AD in association with the arachidonic acid cascade. In addition, it has been suggested that alterations in the balance of polyunsaturated fatty acids are associated with brain dysfunctions such as neurodegerative pathologies of the aging brain. Method: To explore COX-2 expression in the hippocampus, we analyzed 45 consecutive autopsy subjects without dementia and 25 AD patients derived from the town of Hisayama, Japan. Results: The neuronal expression of COX-2 in the CA3 subdivision of the hippocampus, subiculum, entorhinal cortex and transentorhinal cortex were consistently observed in both nondemented and AD brains, and COX-2 immunoreactivity correlated with age in nondemented brains. In AD patients, neurons of CA1 exhibited increased COX-2 immunoreactivity which correlated with the severity of AD pathology. This correlation was not apparent in nondemented subjects. Conclusion: These results suggest that COX-2 expression may be differentially regulated among subdivisions of the hippocampus and that elevated COX-2 expression in the CA1 of AD brains may be associated with AD pathology and thus cognitive dysfunction.

本文言語英語
ページ(範囲)423-431
ページ数9
ジャーナルDementia and Geriatric Cognitive Disorders
23
6
DOI
出版ステータス出版済み - 5月 2007

!!!All Science Journal Classification (ASJC) codes

  • 老年医学
  • 認知神経科学
  • 精神医学および精神衛生

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