Effects of Steaming Time and Frequency for Manufactured Red Liriope platyphylla on the Insulin Secretion Ability and Insulin Receptor Signaling Pathway.
10.5625/lar.2011.27.2.117
- Author:
Sun Il CHOI
1
;
Hye Ryun LEE
;
Jun Seo GOO
;
Ji Eun KIM
;
So Hee NAM
;
In Sik HWANG
;
Young Ju LEE
;
So Hae PRAK
;
Hee Seob LEE
;
Jong Sup LEE
;
In Surk JANG
;
Hong Ju SON
;
Dae Youn HWANG
Author Information
1. College of Natural Resources and Life Science, Pusan National University, Miryang, Republic of Korea. dyhwang@pusan.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Liriope platyphylla;
diabetes;
steaming process;
insulin;
glucose
- MeSH:
Animals;
Asthma;
Down-Regulation;
Glucose;
Glucose Transport Proteins, Facilitative;
Insulin;
Medicine, East Asian Traditional;
Mice;
Mice, Inbred ICR;
Neurodegenerative Diseases;
Phosphorylation;
Receptor, Insulin;
Steam;
Streptozocin;
Up-Regulation
- From:Laboratory Animal Research
2011;27(2):117-126
- CountryRepublic of Korea
- Language:English
-
Abstract:
In oriental medicine, Liriope platyphylla (LP) has long been regarded as a curative herb useful for the treatment of diabetes, asthma, and neurodegenerative disorders. The principal objective of this study was to assess the effects of steaming time and frequency for manufactured Red LP (RLP) on insulin secretion ability and insulin receptor signaling pathway. To achieve our goal, several types of LPs manufactured under different conditions were applied to INS cells and streptozotocin (STZ)-induced diabetic ICR mice, after which alterations in insulin concentrations were detected in the culture supernatants and sera. The optimal concentration for the investigation of insulin secretion ability was found to be 50 ug/mL of LP. At this concentration, maximum insulin secretion was observed in the INS cells treated with LP extract steamed for 3 h (3-SLP) with two repeated steps (3 h steaming and 24 h air-dried) carried out 9 times (9-SALP); no significant changes in viability were detected in any of the treated cells. Additionally, the expression and phosphorylation levels of most components in the insulin receptor signaling pathway were increased significantly in the majority of cells treated with steaming-processed LP as compared to the cells treated with LP prepared without steaming. With regard to glucose transporter (GLUT) expression, alterations of steaming time induced similar responses on the expression levels of GLUT-2 and GLUT-3. However, differences in steaming frequency were also shown to induce dose-dependent responses in the expression level of GLUT-2 only; no significant differences in GLUT-3 expression were detected under these conditions. Furthermore, these responses observed in vitro were similarly detected in STZ-induced diabetic mice. 24-SLP and 9-SALP treatment applied for 14 days induced the down-regulation of glucose concentration and upregulation of insulin concentration. Therefore, these results indicated that the steaming processed LP may contribute to the relief of diabetes symptoms and should be regarded as an excellent candidate for a diabetes treatment.
