Inhibitory effects of oleanane-type triterpenes and saponins from the stem bark of Kalopanax pictus on LPS-stimulated pro-inflammatory cytokine production in bone marrow-derived dendritic cells |
| |
Authors: | Tran Hong Quang Nguyen Thi Thanh Ngan Chau Van Minh Phan Van Kiem Nguyen Xuan Nhiem Bui Huu Tai Nguyen Phuong Thao Doobyeong Chae Vivek Bhakta Mathema Young-Sang Koh Je-Hyun Lee Seo Young Yang Young Ho Kim |
| |
Affiliation: | 1. College of Pharmacy, Chungnam National University, Daejeon, 305-764, Korea 2. Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Caugiay, Hanoi, Vietnam 3. School of Medicine, Brain Korea 21 Program, Institute of Medical Science, Jeju National University, Jeju, 690-756, South Korea 4. College of Oriental Medicine, Dongguk University, Gyeongju, 780-714, Korea
|
| |
Abstract: | ![]() Kalopanax pictus (Araliaceae) is a deciduous tree distributed in Korea, Japan, and China. The stem bark of K. pictus has been functionally used as a traditional crude drug for the treatment of various inflammatory diseases. In the present study, we describe the inhibitory effects of oleanane-type triterpenes and saponins isolated from the stem bark of K. pictus on production of pro-inflammatory cytokines in LPS-stimulated bone marrow-derived dendritic cells. Of the compounds tested, 16,23,29-trihydroxy-3-oxo-olean-12-en-28-oic acid (1), 4,23,29-trihydroxy-3,4-seco-olean-12-en-3-oate-28-oic acid (2), 3β,6β,23-trihydroxyolean-12-en-28-oic acid 28-O-β-D-glucopyranoside (3), nipponogenin E (6), 3β,6β,23-trihydroxyolean-12-en-28-oic acid (7), and caulophyllogenin (19) significantly inhibited the production of IL-12 p40 and IL-6 with IC50 values ranging from 3.3 to 9.1 μM. Compounds 2, 3, 7, and 19 significantly suppressed the secretion of TNF-α with IC50 ranging from 8.8 to 20.0 μM. These data provide scientific support for the use of K. pictus stem bark and its triterpene and saponin components in the inhibition of pro-inflammatory cytokine secretion, including IL-12 p40, IL-6, and TNF-α, and for prevention and treatment of inflammatory diseases. |
| |
Keywords: | |
本文献已被 SpringerLink 等数据库收录! |
|