| Literature DB >> 24060215 |
Su Hyun Park1, Hyun Jae Lee1, Jiho Ryu1, Kun Ho Son2, Sang Yong Kwon2, Sang Kook Lee3, Yeong Shik Kim3, Jang-Hee Hong1, Jeong Ho Seok1, Choong Jae Lee4.
Abstract
In the present study, we investigated whether aqueous extract of Liriope Tuber, ophiopogonin D and spicatoside A derived from Liriope Tuber affect basal or phorbol ester (phorbol 12-myristate 13-acetate, PMA)-induced airway mucin production and secretion from airway epithelial cells. Confluent NCI-H292 cells were treated with each agent for 24 h (basal production) or pretreated with each agent for 30 min and then stimulated with PMA for 24 h (PMA-induced production and secretion), respectively. MUC5AC airway mucin production and secretion were measured by ELISA. The results were as follows: (1) aqueous extract of Liriope Tuber stimulated basal mucin production and did not inhibit but increased PMA-induced mucin production; (2) ophiopogonin D and spicatoside A stimulated basal mucin production and did not inhibit but increased PMA-induced mucin production; (3) two compounds increased PMA-induced mucin secretion. These results suggest that ophiopogonin D and spicatoside A can increase mucin production and secretion, by directly acting on airway epithelial cells and, at least in part, explain the traditional use of aqueous extract of Liriope Tuber as expectorants in diverse inflammatory pulmonary diseases.Entities:
Keywords: Airway mucin; EGF; ELISA; Liriope tuber; Ophiopogonin D; PBS; PMA; RT-PCR; Spicatoside A; enzyme-linked immunosorbent assay; epidermal growth factor; phorbol 12-myristate 13-acetate; phosphate-buffered saline; reverse transcription-polymerase chain reaction
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Year: 2013 PMID: 24060215 DOI: 10.1016/j.phymed.2013.08.013
Source DB: PubMed Journal: Phytomedicine ISSN: 0944-7113 Impact factor: 5.340