Sodium butyrate has context-dependent actions on dipeptidyl peptidase-4 and other metabolic parameters.
10.4196/kjpp.2017.21.5.519
- Author:
Eun Sol LEE
1
;
Dong Sung LEE
;
Prakash Raj PANDEYA
;
Youn Chul KIM
;
Dae Gil KANG
;
Ho Sub LEE
;
Byung Chul OH
;
Dae Ho LEE
Author Information
1. College of Pharmacy, Wonkwang University, Iksan 54538, Korea.
- Publication Type:Original Article
- Keywords:
Dipeptidyl peptidase 4;
HepG2 cells;
Mesangial cells;
Obesity;
Sodium butyrate
- MeSH:
Animals;
Blood Cells;
Blood Glucose;
Body Weight;
Butyric Acid*;
Cytokines;
Diet;
Dipeptidyl Peptidase 4;
Hep G2 Cells;
In Vitro Techniques;
Insulin;
Interleukin-6;
Kidney;
Liver;
Mesangial Cells;
Metabolic Diseases;
Mice;
Mice, Obese;
Obesity;
RNA, Messenger;
Sodium*
- From:The Korean Journal of Physiology and Pharmacology
2017;21(5):519-529
- CountryRepublic of Korea
- Language:English
-
Abstract:
Sodium butyrate (SB) has various metabolic actions. However, its effect on dipeptidyl peptidase 4 (DPP-4) needs to be studied further. We aimed to evaluate the metabolic actions of SB, considering its physiologically relevant concentration. We evaluated the effect of SB on regulation of DPP-4 and its other metabolic actions, both in vitro (HepG2 cells and mouse mesangial cells) and in vivo (high fat diet [HFD]-induced obese mice). Ten-week HFD-induced obese C57BL/6J mice were subjected to SB treatment by adding SB to HFD which was maintained for an additional 16 weeks. In HepG2 cells, SB suppressed DPP-4 activity and expression at sub-molar concentrations, whereas it increased DPP-4 activity at a concentration of 1,000 µM. In HFD-induced obese mice, SB decreased blood glucose, serum levels of insulin and IL-1β, and DPP-4 activity, and suppressed the increase in body weight. On the contrary, various tissues including liver, kidney, and peripheral blood cells showed variable responses of DPP-4 to SB. Especially in the kidney, although DPP-4 activity was decreased by SB in HFD-induced obese mice, it caused an increase in mRNA expression of TNF-α, IL-6, and IL-1β. The pro-inflammatory actions of SB in the kidney of HFD-induced obese mice were recapitulated by cultured mesangial cell experiments, in which SB stimulated the secretion of several cytokines from cells. Our results showed that SB has differential actions according to its treatment dose and the type of cells and tissues. Thus, further studies are required to evaluate its therapeutic relevance in metabolic diseases including diabetes and obesity.
