1. Academic Validation
  2. The Inhibitory Effect of Alisol A 24-Acetate from Alisma canaliculatum on Osteoclastogenesis

The Inhibitory Effect of Alisol A 24-Acetate from Alisma canaliculatum on Osteoclastogenesis

  • Int J Endocrinol. 2015:2015:132436. doi: 10.1155/2015/132436.
Kwang-Jin Kim 1 Alain Simplice Leutou 2 Jeong-Tae Yeon 3 Sik-Won Choi 4 Seong Hwan Kim 4 Sung-Tae Yee 1 Kyung Hee Choi 1 Sang-Jip Nam 2 Young-Jin Son 1
Affiliations

Affiliations

  • 1 Department of Pharmacy, Sunchon National University, Suncheon, Jeonnam 540-742, Republic of Korea.
  • 2 Department of Chemistry and Nano Science, Global Top 5 Program, Ewha Womans University, Seoul 120-750, Republic of Korea.
  • 3 Research Institute of Basic Science, Sunchon National University, Suncheon 540-742, Republic of Korea.
  • 4 Laboratory of Translational Therapeutics, Pharmacology Research Center, Division of Drug Discovery Research, Korea Research Institute of Chemical Technology, Daejeon 305-600, Republic of Korea.
Abstract

Osteoporosis is a disease that decreases bone mass. The number of patients with osteoporosis has been increasing, including an increase in patients with bone fractures, which lead to higher medical costs. Osteoporosis treatment is all-important in preventing bone loss. One strategy for osteoporosis treatment is to inhibit osteoclastogenesis. Osteoclasts are bone-resorbing multinucleated cells, and overactive osteoclasts and/or their increased number are observed in bone disorders including osteoporosis and rheumatoid arthritis. Bioactivity-guided fractionations led to the isolation of alisol A 24-acetate from the dried tuber of Alisma canaliculatum. Alisol A 24-acetate inhibited RANKL-mediated osteoclast differentiation by downregulating NFATc1, which plays an essential role in osteoclast differentiation. Furthermore, it inhibited the expression of DC-STAMP and Cathepsin K, which are related to cell-cell fusion of osteoclasts and bone resorption, respectively. Therefore, alisol A 24-acetate could be developed as a new structural scaffold for inhibitors of osteoclast differentiation in order to develop new drugs against osteoporosis.

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