scholarly journals Therapeutic Effects of Momordica charantia L. Ethanolic Extract on Acetic Acid-Induced Ulcerative Colitis in Rats

2021 ◽  
Vol 0 (0) ◽  
pp. 119-128
Author(s):  
Dilek Özbeyli ◽  
Ali Şen ◽  
Aslı Aykaç ◽  
Kerem Teralı ◽  
Özlem Çilingir Kaya ◽  
...  
2018 ◽  
Vol 13 (3) ◽  
pp. 241
Author(s):  
Bharati Zaware ◽  
Ritu Gilhotra ◽  
Sanjay Ravindra Chaudhari

<p class="Abstract">The aim of present investigation was to validate its folk use in the treatment of ulcerative colitis in the rat model. Sprague Dawley rats were divided into nine groups with six animals in each group. The rats received seven days of pretreatment with chloroform, ethyl acetate or ethanolic extract of <em>Mimosa pudica</em>. For induction of ulcerative colitis, rats were administered with 2 mL of 4% acetic acid solution intrarectally. Ulcer index, macroscopical study of the colon, myeloperoxidase and malondialdehyde levels in colon tissue and blood, and histopathology of the colon tissue were studied. Intrarectal instillation of acetic acid caused increased ulcer index, colonic myeloperoxidase and malondialdehyde. Pretreatment with <em>M. pudica</em> ethanolic extract (400 mg/kg) significantly lowered the ulcer index, colonic myeloperoxidase and malondialdehyde as compared with the standard drug prednisolone. The present investigation demonstrates that the ethanol extract of <em>M. pudica</em> leaf is effective in the treatment of ulcerative colitis.</p><p class="Abstract"><strong>Video Clip of Methodology:</strong></p><p class="Abstract">Embedding or block making: 24 sec   <a href="https://www.youtube.com/v/Y1I4tKYMLsE">Full Screen</a>   <a href="https://www.youtube.com/watch?v=Y1I4tKYMLsE">Alternate</a></p><p class="Abstract">Tissue processing: 19 sec   <a href="https://www.youtube.com/v/7nYpxL2qPhg">Full Screen</a>   <a href="https://www.youtube.com/watch?v=7nYpxL2qPhg">Alternate</a></p><p class="Abstract">Section cutting: 33 sec   <a href="https://www.youtube.com/v/_amFL9kNLBw">Full Screen</a>   <a href="https://www.youtube.com/watch?v=_amFL9kNLBw">Alternate</a></p>


2020 ◽  
Vol 12 (3) ◽  
pp. 154-161 ◽  
Author(s):  
Negar Hassanshahi ◽  
Seyed Jalil Masoumi ◽  
Davood Mehrabani ◽  
Seyedeh Sara Hashemi ◽  
Morteza Zare

BACKGROUND The use of herbal and synthetic compounds can be effective in improving the areas and repair of tissues that have been affected during the processes like what happens in ulcerative colitis (UC) as a common inflammatory disorder. According to the beneficial effects of aloe vera, in this study, we aimed to assess the therapeutic effects of oral aloe vera gel on acetic acid-induced colitis in rats by histopathological and molecular analysis of Bax, and BCL-2 genes expression (using RT-PCR technique) in colon tissue samples. METHODS This experimental study comprised 32 adult male Sprague Dawley rats weighting 220 ± 20 g that were randomly divided into four groups as follows. The control group (healthy rats), colitis group in which UC was induced by transrectal administration of 3% acetic acid with no treatment, oral form of sulfasalazine group in which UC was induced by transrectal administration of 3% acetic acid, then was treated by oral administration of sulfasalazine 500 mg/kg body weight, and the fourth group which received oral form of aloe vera gel (200 mg / kg) for 21 days, respectively after induction of UC. Then, the therapeutic effects of treatment groups were compared with the control group and the colitis group with no treatment, by the assessment of histopathological and molecular changes in the colon tissues of rats on the 7th, 14th, and 21st days. Finally, the collected data were analyzed using statistical tests. RESULTS Histologically, aloe vera gel treatment could reduce and heal colon tissue damages in induced colitis. Also, this gel reduced apoptosis in rat’s colon with acetic acid-induced colitis, which showed in significantly decreased in Bax mRNA expression and significantly increased BCL-2 mRNA expression compared with the colitis group with no treatment. CONCLUSION Aloe vera gel has a significant effect on the treatment of UC in rat because of the beneficial effect that was found from aloe vera such as decreasing the severity of colitis as evidenced by histopathological findings, and with respect to apoptosis and gene expression that were related to wound healing process, and suppression of the elevation of Bax mRNA with the upregulation of Bcl-2, which can be considered effective in the treatment of UC.


2020 ◽  
Vol 9 (3) ◽  
pp. 223
Author(s):  
Gholamreza Bahrami ◽  
Hossein Malekshahi ◽  
Shahram Miraghaee ◽  
Hamid Madani ◽  
Atefeh Babaei ◽  
...  

Author(s):  
Michel Archange Fokam Tagne ◽  
Anatole Tchoffo ◽  
Paul Aimé Noubissi ◽  
Aimée Gisolène Mazo ◽  
Blaise Kom ◽  
...  

2013 ◽  
Vol 32 (4) ◽  
pp. 926-930 ◽  
Author(s):  
XIAO KE ◽  
FAN ZHOU ◽  
YOULIANG GAO ◽  
BINGYING XIE ◽  
GUANGHONG HU ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ning Li ◽  
Yichi Zhang ◽  
Narayan Nepal ◽  
Guoqing Li ◽  
Ningning Yang ◽  
...  

Abstract Background Ulcerative colitis (UC) is a chronic and recurrent disease without satisfactory treatment strategies. Dental pulp stem cell (DPSC) transplantation has been proposed as a potential therapy for UC. This study aimed to investigate the therapeutic effects of the rat hepatocyte growth factor (HGF) gene transduced into DPSCs for UC. Methods The therapeutic effects of HGF-DPSCs transplanted intravenously into a rat model of UC induced by 5% dextran sulphate sodium (DSS) were compared with the other treatment groups (LV-HGF group, DPSCs group and GFP-DPSCs group). Immunofluorescence and immunohistochemistry were used to observe the localization and proliferation of HGF-DPSCs at the site of colon injury. The expression levels of inflammatory factors were detected by real-time quantitative PCR (RT-PCR) and western blotting. The oxidative stress markers were detected by ELISA. DAI scores and body weight changes were used to macroscopically evaluate the treatment of rats in each group. Results Immunofluorescence and immunohistochemistry assays showed that HGF-DPSCs homed to colon injury sites and colocalized with intestinal stem cell (ISC) markers (Bmi1, Musashi1 and Sox9) and significantly promoted protein expression (Bmi1, Musashi1, Sox9 and PCNA). Anti-inflammatory cytokine (TGF-β and IL-10) expression was the highest in the HGF-DPSCs group compared with the other treatment groups, while the expression of pro-inflammatory cytokines (TNF-α and INF-γ) was the lowest. Additionally, the oxidative stress response results showed that malondialdehyde (MDA) and myeloperoxidase (MPO) expression decreased while superoxide dismutase (SOD) expression increased, especially in the HGF-DPSCs group. The DAI scores showed a downward trend with time in the five treatment groups, whereas body weight increased, and the changes were most prominent in the HGF-DPSCs group. Conclusions The study indicated that HGF-DPSCs can alleviate injuries to the intestinal mucosa by transdifferentiating into ISC-like cells, promoting ISC-like cell proliferation, suppressing inflammatory responses and reducing oxidative stress damage, which provides new ideas for the clinical treatment of UC.


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