scholarly journals Therapeutic Potency of Gallium verum Extract on Ethanol-Induced Gastric Ulcer in Rats

2021 ◽  
Vol 12 (5) ◽  
pp. 6010-6020
Keyword(s):  
Gastric Juice ◽  
Gastric Ulcers ◽  
Ethanol Administration ◽  
Gastric Injury ◽  
Glutathione S Transferase ◽  
Histological Lesion ◽  
Immunohistochemical Markers ◽  
Ulcer Group ◽  
Tnf Α ◽  
Promising Treatment

Gallium verum, lady's bedstraw is an herbaceous annual plant belonging to the genus Rubiaceae; it possessed antioxidant, cytotoxic for cancer cells, antimicrobial, protective and endocrine effects. This work aimed to investigate the curative effects of G. verum extract on gastric ulcers following absolute ethanol administration in the healthy rat. Eighteen rats were randomly divided into three main groups; rats were fastened for 24 hours before ethanol administration. All groups except control administered ethanol (5 ml/kg body weight; orally). The rats were administrated distilled water (Ulcer group) or G. verum extract (100mg/kg) one hour later. G. verum extract caused a significant decrease in ulcer index, gastric juice volume, malondialdehyde, and nitric oxide, while gastric juice pH, glutathione, glutathione-S-transferase, and catalase increased significantly. The histological lesion score showed a significant enhancement in group G. verum compared to the ulcer group that scored the highest pathological destruction score. Immunohistochemical markers of NF-κB p65 and TNF-α showed a significant decrease in G. verum group. G. verum extract is a promising treatment modality against gastric injury through its powerful antioxidant, acid neutralizing, healing promotion, and ant-inflammation effects.

scholarly journals Methanolic Extract of Distemonanthus benthamianus (Caesalpiniaceae) Stem Bark Suppresses Ethanol/Indomethacin-Induced Chronic Gastric Injury in Rats

2020 ◽  
Vol 2020 ◽  
pp. 1-14
Author(s):  
Vanessa Mba Matah Marte ◽  
Gilbert Ateufack ◽  
Marius Mbiantcha ◽  
Albert Donatien Atsamo ◽  
Carine Flore Adjouzem ◽  
...  
Keyword(s):  
Methanolic Extract ◽  
Protein Denaturation ◽  
Hematological Parameters ◽  
Mechanisms Of Action ◽  
Male Rats ◽  
Gastric Ulcers ◽  
Gastric Injury ◽  
Ros Production ◽  
Tnf Α ◽  
Anti Inflammatory

Distemonanthus benthamianus (Caesalpiniaceae) is a plant from the Cameroon pharmacopoeia very widely used in the treatment of many pathologies among which are gastrointestinal disorders. The main purpose of this study was to assess the healing properties of gastric ulcer from the methanolic extract of Distemonanthus benthamianus and its mechanisms of action. The healing properties of gastric ulcers (chronic ulcer model induced by ethanol and indomethacin) were evaluated in vivo in adult male rats, while the mechanisms of action were evaluated in vitro by anti-inflammatory assay (protein denaturation, cyclooxygenase, and lipoxygenase assays) and immunomodulatory assay (ROS production (using technical chemiluminescence), cytokine (TNF-α, IL-1β, IL-6) production (using ELISA), proliferation of T cells (using liquid scintillation counter), and cytotoxicity (using MTT assay)). The methanolic extract of Distemonanthus benthamianus inhibited protein denaturation (75.63%) and the activities of cyclooxygenase (78.92%) and 5-lipoxygenase (81.54%). The extract also significantly ( p < 0.001 ) inhibited intracellular and extracellular ROS production and T cell proliferation and reduced significantly ( p < 0.01 , p < 0.001 ) TNF-α, IL-1β, IL-6, and PGE2 production. At all doses (125, 250, and 500 mg/kg), the extract significantly reduces the ulceration index and the area of ulceration and significantly increases the mass of gastric mucus. In addition, the extract significantly decreases the level of MDA, significantly increases the activities of catalase and glutathione, and then improves the hematological parameters in sick animals. Histological micrographs show that in the presence of the extract, there is advanced reepithelialization with recovery of the ulcerated epithelium. Thus, the extract of Distemonanthus benthamianus has healing properties against gastric ulcers which are associated with its anti-inflammatory, immunomodulatory, and antioxidant effects.

scholarly journals Gastroprotective Effect of Sinapic Acid on Ethanol-Induced Gastric Ulcers in Rats: Involvement of Nrf2/HO-1 and NF-κB Signaling and Antiapoptotic Role

2021 ◽  
Vol 12 ◽  
Author(s):  
Mohammad Raish ◽  
Mudassar Shahid ◽  
Yousef A. Bin Jardan ◽  
Mushtaq Ahmad Ansari ◽  
Khalid M. Alkharfy ◽  
...  
Keyword(s):  
Lipid Peroxidation ◽  
Gastric Juice ◽  
Caspase 3 ◽  
Sinapic Acid ◽  
Gastric Ulcers ◽  
Nuclear Factor ◽  
Total Acidity ◽  
Free Acidity ◽  
Tnf Α ◽  
Gastric Juice Volume

Background: In the current study, we evaluated the therapeutic potential of sinapic acid (SA) in terms of the mechanism underlying its gastroprotective action against ethanol-induced gastric ulcers in rats.Methods: These effects were examined through gross macroscopic evaluation of the stomach cavity [gastric ulcer index (GUI)], alteration in pH, gastric juice volume, free acidity, total acidity, total gastric wall mucus, and changes in PGE2. In addition, we evaluated lipid peroxidation (malondialdehyde), antioxidant systems (catalase and glutathione), inflammatory markers [tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), and myeloperoxidase (MPO)], apoptotic markers (caspase-3, Bax, and Bcl-2), nuclear factor-κB [NF-κB (p65)], NO levels, and histopathological staining (H and E and PAS).Results: In rats with ethanol-induced ulcers, pre-treatment with SA (40 mg/kg p. o.) decreased the sternness of ethanol-induced gastric mucosal injuries by decreasing the GUI, gastric juice volume, free acidity, and total acidity. In addition, the pH and total gastric mucosa were increased, together with histopathological alteration, neutrophil incursion, and increases in PGE2 and NO2. These effects were similar to those observed for omeprazole, a standard anti-ulcer drug. SA was shown to suppress gastric inflammation through decreasing TNF-α, IL-6, and MPO, as well as curbing gastric oxidative stress through the inhibition of lipid peroxidation (MDA) and restoration of depleted glutathione and catalase activity. SA inhibited Bcl-2-associated X (Bax) and caspase-3 activity, and restored the antiapoptotic protein Bcl-2; these findings indicate the antiapoptotic potential of SA, leading to enhanced cell survival. SA also repressed NF-κB signaling and increased IκBα. Moreover, SA upregulated the nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1), thereby restoring depleted antioxidant defense enzymes and implicating the NRF2/HO-1 signaling pathways.Conclusion: These results suggest that the prophylactic administration of SA (40 mg/kg) can ameliorate ethanol-induced gastric ulcers in rats primarily via the modulation of Nrf2/HO-1 and NF-κB signaling and subsequent enhancement of cell viability.

scholarly journals Preventive Effect of Liupao Tea Polyphenols on HCl/Ethanol-Induced Gastric Injury in Mice

2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Kai Zhu ◽  
Peng Peng ◽  
Ning Wu ◽  
Xianrong Zhou ◽  
Jianfei Mu ◽  
...  
Keyword(s):  
Gastric Juice ◽  
Tea Polyphenols ◽  
Gastric Injury ◽  
Mouse Serum ◽  
Gastric Tissue ◽  
Preventive Effect ◽  
High Concentration ◽  
Sod Activity ◽  
Bioactive Substances ◽  
Gastric Mucosal Lesions

Liupao tea is a traditional Chinese tea drink. The preventive effect of crude polyphenols in Liupao tea on HCl/ethanol-induced gastric injury was investigated in this study. After a model of gastric injury in mice was established, mouse serum and tissues were analyzed by biochemical and molecular biological methods. The results showed that Liupao tea polyphenols (LTPs) could effectively reduce the area of gastric mucosal lesions, decrease the volume of gastric juice, and increase the pH of gastric juice in mice with gastric injury. Observations of the pathology revealed that LTPs could alleviate cell necrosis and gastric mucosal injury in mice with gastric injury. The SOD activity and GSH level were decreased in mice after gastric injury, while the level of MDA was increased. LTPs could inhibit the changes caused by gastric injury and make the SOD activity, GSH, and MDA levels close to the normal levels. In addition, LTPs could upregulate the mRNA expression of Cu/Zn-SOD, Mn-SOD, CAT, nNOS, and eNOS and downregulate the expression of iNOS in the gastric tissue of mice with gastric injury. Therefore, LTPs can effectively prevent HCl/ethanol-induced gastric injury. HPLC analysis showed that LTP contains six bioactive substances of gallic acid, catechin, caffeine, epicatechin, epigallocatechin gallate, and epicatechin gallate, so the effect of LTP might mainly come from these six components. The effect of a high concentration of LTP is similar to that of ranitidine. LTPs represent a kind of active substance with a protective effect on gastric tissue.

Radiotherapy for gastric ulcers in the light of radiobiology and clinical data

1934 ◽  
Vol 30 (2) ◽  
pp. 310-316
Author(s):  
R. Ya. Gasul
Keyword(s):  
Gastric Juice ◽  
Clinical Data ◽  
Gastric Ulcers ◽  
Malignant Neoplasms ◽  
X Rays

In spite of the fact that already in 1913 the first quite successful attempts were made to treat gastric ulcers with X-rays (Kodo) and to influence the secretion and acidity of gastric juice with the help of illumination (Brgel, 1916), the clinic has not yet shown sufficient interest in the use of X-rays in the treatment of ulcers and their complications. Some clinicians still believe that only malignant neoplasms are treated with X-rays, and only those that are rejected by surgeons.

scholarly journals Succinamide Derivatives Ameliorate Neuroinflammation and Oxidative Stress in Scopolamine-Induced Neurodegeneration

Biomolecules ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 443 ◽  
Author(s):  
Sumbal Iqbal ◽  
Fawad Ali Shah ◽  
Komal Naeem ◽  
Humaira Nadeem ◽  
Sadia Sarwar ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Neuronal Injury ◽  
Binding Affinities ◽  
Glutathione S Transferase ◽  
In Vivo Experiments ◽  
Tnf Α ◽  
And Oxidative Stress ◽  
Necrosis Factor

Oxidative stress-mediated neuroinflammatory events are the hallmark of neurodegenerative diseases. The current study aimed to synthesize a series of novel succinamide derivatives and to further investigate the neuroprotective potential of these compounds against scopolamine-induced neuronal injury by in silico, morphological, and biochemical approaches. The characterization of all the succinamide derivatives was carried out spectroscopically via proton NMR (1H-NMR), FTIR and elemental analysis. Further in vivo experiments showed that scopolamine induced neuronal injury, characterized by downregulated glutathione (GSH), glutathione S-transferase (GST), catalase, and upregulated lipid peroxidation (LPO). Moreover, scopolamine increased the expression of inflammatory mediators such as cyclooxygenase2 (COX2), nuclear factor kappa B (NF-kB), tumor necrosis factor (TNF-α), further associated with cognitive impairment. On the other hand, treatment with succinamide derivatives ameliorated the biochemical and immunohistochemical alterations induced by scopolamine, further supported by the results obtained from molecular docking and binding affinities.

Xanthoangelol Isolated from Angelica keiskei Roots Prevents Dextran Sulfate Sodium-Treated Colitis in Mice

2020 ◽  
Vol 10 (5) ◽  
pp. 655-663
Author(s):  
Yoshiyuki Kimura ◽  
Kimye Baba
Keyword(s):  
Dextran Sulfate ◽  
Dextran Sulfate Sodium ◽  
Activity Index ◽  
Gastrointestinal Diseases ◽  
Gastric Ulcers ◽  
Eosinophil Infiltration ◽  
Full Blood Count ◽  
Therapeutic Effects ◽  
Tnf Α ◽  
Angelica Keiskei

Background: The therapeutic effects of a number of natural products on Inflammatory Bowel Disease (IBD) have recently been examined in detail. The whole herb and roots of Angelica keiskei (Umblliferae) have traditionally been used as a diuretic, to treat gastrointestinal diseases such as gastric ulcers and diarrhea in Japan. Objectives: The present study was performed to investigate the effects of xanthoangelol, a major chalcone of Angelica keiskei roots, on diarrhea and inflammation in the large intestine of IBD model mice. Methods: Xanthoangelol (10 & 25 mg/kg) was orally administered to mice with 3% Dextran Sulfate Sodium (DSS)-induced colitis. Blood samples were collected during the experimental period, subjected to a full blood count test, and colonic cytokine and chemokine levels were measured. Results: Xanthoangelol (25 mg/kg) reduced the Disease Activity Index (DAI) of colitis. It also attenuated DSS-induced reductions in red blood cell and platelet counts as well as Hb and Ht levels. A histological examination of the colon using direct fast scarlet staining showed that xanthoangelol prevented DSS-induced mucosal ulceration and eosinophil infiltration. Xanthoangelol also reduced DSS-induced increases in colonic MCP-1, IL-1β, and TNF-α levels. Conclusions: Xanthoangelol reduced DSS-induced increases in colonic IL-1β, TNF-α, and MCP-1 levels and prevented eosinophil infiltration, which supports its potential as a treatment for IBD.

scholarly journals Hydroxyproline, a Serum Biomarker Candidate for Gastric Ulcer in Rats: A Comparison Study of Metabolic Analysis of Gastric Ulcer Models Induced by Ethanol, Stress, and Aspirin

2014 ◽  
Vol 9 ◽  
pp. BMI.S15918 ◽  
Author(s):  
Kenichiro Takeuchi ◽  
Maki Ohishi ◽  
Keiko Endo ◽  
Kenichi Suzumura ◽  
Hitoshi Naraoka ◽  
...  
Keyword(s):  
Gastric Ulcer ◽  
Gastrointestinal Symptoms ◽  
Drug Effects ◽  
Serum Biomarker ◽  
Gastric Ulcers ◽  
Gastric Injury ◽  
Ethanol Stress ◽  
Metabolomic Profiling ◽  
Inflammatory Drugs ◽  
Common Manifestation

Gastrointestinal symptoms are a common manifestation of adverse drug effects. Non-steroid anti-inflammatory drugs (NSAIDs) are widely prescribed drugs that induce the serious side effect of gastric mucosal ulceration. Biomarkers for these side effects have not been identified and ulcers are now only detectable by endoscopy. We previously identified five metabolites as biomarker candidates for NSAID-induced gastric ulcer using capillary electrophoresis–mass spectrometry (CE–MS)-based metabolomic analysis of serum and stomach from rats. Here, to clarify mechanism of changes and limitations of indications of biomarker candidates, we performed CE–MS-based metabolomic profiling in stomach and serum from rats with gastric ulcers induced by ethanol, stress, and aspirin. The results suggest that a decrease in hydroxyproline reflects the induction of gastric injury and may be useful in identifying gastric ulcer induced by multiple causes. While extrapolation to humans requires further study, hydroxyproline can be a new serum biomarker of gastric injury regardless of cause.

scholarly journals Mechanisms of Gastroprotective Effects of Ethanolic Leaf Extract ofJasminum sambacagainst HCl/Ethanol-Induced Gastric Mucosal Injury in Rats

2012 ◽  
Vol 2012 ◽  
pp. 1-15 ◽  
Author(s):  
Ahmed S. AlRashdi ◽  
Suzy M. Salama ◽  
Salim S. Alkiyumi ◽  
Mahmood A. Abdulla ◽  
A. Hamid A. Hadi ◽  
...  
Keyword(s):  
Gastric Content ◽  
Gastric Wall ◽  
Mucosal Injury ◽  
Ethanol Solution ◽  
Normal Group ◽  
Gastric Mucosal Injury ◽  
Gastric Ulcers ◽  
Prostaglandin E ◽  
Bax Protein ◽  
Ulcer Group

Jasminum sambacis used in folk medicine as the treatment of many diseases. The aim of the present investigation is to evaluate the gastroprotective effects of ethanolic extracts ofJ. sambacleaves against acidified ethanol-induced gastric ulcers in rats. Seven groups of rats were orally pre-treated with carboxymethylcellulose (CMC) as normal group, CMC as ulcer group, 20 mg/kg of omeprazole as positive group, 62.5, 125, 250, and 500 mg/kg of extract as the experimental groups, respectively. An hour later, CMC was given orally to normal group and acidified ethanol solution was given orally to the ulcer control, positive control, and the experimental groups. The rats were sacrificed after an hour later. Acidity of gastric content, the gastric wall mucus, ulcer areas, and histology and immunohistochemistry of the gastric wall were assessed. Gastric homogenates were determined for prostaglandin E2(PGE2), superoxide dismutase (SOD), andmalondialdehyde (MDA) content. Ulcer group exhibited significantly severe mucosal injury as compared with omeprazole or extract which shows significant protection towards gastric mucosal injury the plant promotes ulcer protection as it shows significant reduction of ulcer area grossly, and histology showed marked reduction of edema and leucocytes infiltration of submucosal layer compared with ulcer group. Immunohistochemistry showed overexpression of Hsp70 protein and downexpression of Bax protein in rats pretreated with extract. Significant increased in the pH, mucus of gastric content and high levels of PGE2, SOD and reduced amount of MDA was observed.

scholarly journals Anti-inflammatory effects of angiotensin II AT1 receptor antagonism prevent stress-induced gastric injury

2003 ◽  
Vol 285 (2) ◽  
pp. G414-G423 ◽  
Author(s):  
Claudia Bregonzio ◽  
Ines Armando ◽  
Hiromichi Ando ◽  
Miroslava Jezova ◽  
Gustavo Baiardi ◽  
...  
Keyword(s):  
Blood Flow ◽  
Angiotensin Ii ◽  
Gastric Mucosa ◽  
Restraint Stress ◽  
Neutrophil Infiltration ◽  
Gastric Blood Flow ◽  
Gastric Injury ◽  
Tnf Α ◽  
Cold Restraint Stress ◽  
Cold Restraint

Stress reduces gastric blood flow and produces acute gastric mucosal lesions. We studied the role of angiotensin II in gastric blood flow and gastric ulceration during stress. Spontaneously hypertensive rats were pretreated for 14 days with the AT1 receptor antagonist candesartan before cold-restraint stress. AT1 receptors were localized in the endothelium of arteries in the gastric mucosa and in all gastric layers. AT1 blockade increased gastric blood flow by 40–50%, prevented gastric ulcer formation by 70–80% after cold-restraint stress, reduced the increase in adrenomedullary epinephrine and tyrosine hydroxylase mRNA without preventing the stress-induced increase in adrenal corticosterone, decreased the stress-induced expression of TNF-α and that of the adhesion protein ICAM-1 in arterial endothelium, decreased the neutrophil infiltration in the gastric mucosa, and decreased the gastric content of PGE2. AT1 receptor blockers prevent stress-induced ulcerations by a combination of gastric blood flow protection, decreased sympathoadrenal activation, and anti-inflammatory effects (with reduction in TNF-α and ICAM-1 expression leading to reduced neutrophil infiltration) while maintaining the protective glucocorticoid effects and PGE2 release. Angiotensin II has a crucial role, through stimulation of AT1 receptors, in the production and progression of stress-induced gastric injury, and AT1 receptor antagonists could be of therapeutic benefit.

Prophylactic Effect of Dragon-Pearl Tea on HCl/Ethanol Induced Gastric Injury in ICR Mice

2014 ◽  
Vol 651-653 ◽  
pp. 273-276
Author(s):  
Rui Wang ◽  
Xin Zhao
Keyword(s):  
Gastric Secretion ◽  
Inhibitory Effect ◽  
Gastric Injury ◽  
Prophylactic Effect ◽  
Preventive Effect ◽  
Icr Mice ◽  
Low Concentrations ◽  
Tnf Α ◽  
High Concentrations ◽  
Preventive Effects

Dragon-pearl tea is a traditional Chinese drink consumed in Southwest of China. In the present study, the preventive effect of Dragon-pearl tea on gastric injury was determined in ICR mice. High concentrations of Dragon-pearl tea were observed to reduce the levels of the serum proinflammatory cytokines, IL-6 and TNF-α, compared with low concentrations of Dragon-pearl tea. Gastric secretion volumes were highest in control mice and reduced in 500, 1,000 and 1,500 mg/kg Dragon-pearl tea treated mice. The pH levels of gastric juice samples obtained from each group revealed the opposite correlation. Gastric injury levels in mice treated with Dragon-pearl tea were identified to be significantly reduced, demonstrating its anti-inflammatory properties. Administration of 1,500 mg Dragon-pearl tea (79.4%) by gavage was demonstrated to induce the highest inhibitory effect on gastric injury. Results of the current study indicate that Dragon-pearl tea exhibits marked preventive effects on gastric injury.

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