scholarly journals Oral administration of Lactobacillus�plantarum 06CC2 prevents experimental colitis in mice via an anti‑inflammatory response

Author(s):  
Akihito Tanaka ◽  
Shuji Kanmura ◽  
Yuko Morinaga ◽  
Katsuto Kawabata ◽  
Shiho Arima ◽  
...  
2020 ◽  
Vol 21 (23) ◽  
pp. 9283
Author(s):  
Mijin Kwon ◽  
Jaehoon Lee ◽  
Sangkyu Park ◽  
Oh-Hee Kwon ◽  
Jeongmin Seo ◽  
...  

Inflammation is a biological response of the immune system to defend the body from negative stimulation. However, the excessive inflammatory response can damage host tissues and pose serious threats. Exopolysaccharide (EPS), one of the postbiotics, is secreted from lactic acid bacteria. Although many studies have described the beneficial effects of EPS, such as its anti-inflammatory and anti-oxidant effects, its underlying mechanisms have remained to be poorly understood. Thus, we identified that EPS obtained from Lactobacillus plantarum L-14 was a homogeneous polysaccharide primarily comprised of glucose. To examine these anti-inflammatory effects, an inflammatory response was induced by lipopolysaccharide (LPS) administration to mouse macrophage RAW 264.7 cells that were pretreated with EPS. The anti-inflammatory effects of EPS were identified by analyzing the changes within inflammatory markers at the molecular level. We demonstrate here that EPS suppressed proinflammatory mediators, such as cyclooxygenase-2, interleukin-6, tumor necrosis factor-α, and interleukin-1β, and downregulated the expression of an inducible nitric oxide synthase known to lead to oxidative stress. It was also confirmed that EPS had anti-inflammatory effects by blocking the interaction of LPS with Toll-like receptor 4 (TLR4), as demonstrated by using the known TLR4 inhibitor TAK-242. In addition, we found that EPS itself could suppress the expression of TLR4. Consequently, our data suggest that EPS can be a potential target for the development of natural product-derived medicine for treating inflammatory diseases related to TLR4.


2019 ◽  
Vol 67 ◽  
pp. 14-19 ◽  
Author(s):  
Emi Makino ◽  
Tomoki Fukuyama ◽  
Yuko Watanabe ◽  
Risako Tajiki-Nishino ◽  
Hitoshi Tajima ◽  
...  

2020 ◽  
Vol 26 (38) ◽  
pp. 4934-4943
Author(s):  
Mit Joshi ◽  
Neetinkumar D. Reddy ◽  
Nitesh Kumar ◽  
Suhani Sumalatha ◽  
Mallikarjuna Rao Chamallamudi

Background: Histone deacetylase (HDAC) inhibition has been found to be effective in the treatment of inflammatory bowel disease. Previous studies have reported that Cinnamyl sulfonamide hydroxamate derivatives possess non-selective HDAC inhibition. Objective: The present study was designed to screen three selected Cinnamyl sulfonamide hydroxamate derivatives, NMJ-1, NMJ-2, and NMJ3, for in vitro anti-inflammatory response by assessing the expression of pNF-κB in lipopolysaccharide (LPS)-induced inflammatory changes on RAW 264.7 cells, and in vivo anti-inflammatory response in acetic acid (AA) and 2.4-dinitrochlorobenzene (DNCB)-induced colitis models in Wistar rats. Method: AA-induced colitis was produced in Wistar rats by intra-colonic administration of 1 ml AA. DNCBinduced colitis was produced by spraying 250 μL DNCB in acetone (20g/L) on the nape of the rats for 14 days, followed by the intracolonic administration on day 15. Drugs were administered for three days after the induction of colitis. Results: In vitro anti-inflammatory effect was observed by NMJ1 and NMJ2 through a significant decrease in pNF-κB overexpression-induced by LPS. Similar effect was observed in anti-colitis response by NMJ2 in both models by reversing the colitis-induced changes in length, weight, anti-oxidant profile and histopathology of the colon. Conclusion: NMJ2 was found to be most effective among the tested compounds as an anti-inflammatory agent in both in vitro and in vivo inflammatory studies.


Planta Medica ◽  
2007 ◽  
Vol 73 (09) ◽  
Author(s):  
S Popov ◽  
G Popova ◽  
V Golovchenko ◽  
R Ovodova

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