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2.
Phytomedicine ; 55: 31-39, 2019 Mar 01.
Article in English | MEDLINE | ID: mdl-30668441

ABSTRACT

BACKGROUND: Clausena excavata Burm.f. (Rutaceae) has been used for the treatment of stomach disorders including peptic ulcer. PURPOSE: In this study, we aimed to investigate dentatin isolated from C. excavata Burm.f., for anti-ulcer activity against ethanol ulcer model in rats. METHODS: Gastric acid output, ulcer index, serum profile, histological evaluation using Hematoxylin and eosin (HE), periodic acid Schiff base stainings and immunohistochemical localization for heat shock proteins 70 (HSP70) were all investigated. Possible involvement of reduced glutathione (GSH), lipid peroxidation, prostaglandin E2 (PGE2), superoxide dismutase (SOD) enzymes, radical scavenging, and anti-Helicobacter pylori activity were investigated. RESULTS: Dentatin showed anti-secretory activity against the pylorus ligature model and protected the gastric mucosa from ethanol ulceration, as revealed by the improved macroscopic and histological appearance. Dentatin significantly increased the gastric homogenate content of PGE2 GSH and SOD. Dentatin inhibited the lipid peroxidation as revealed by the reduced gastric content of malondialdehyde (MDA). Moreover, dentatin up-regulated HSP70 expression. However, dentatin showed insignificant anti-H. pylori activity. CONCLUSION: Dentatin possesses gastro-protective activity, which could be attributed to the anti-secretory, mucus production, anti-oxidant, and HSP70 activities.


Subject(s)
Anti-Ulcer Agents/pharmacology , Antioxidants/pharmacology , Heterocyclic Compounds, 3-Ring/pharmacology , Stomach Ulcer/drug therapy , Animals , Clausena/chemistry , Ethanol/adverse effects , Female , Gastric Mucosa/drug effects , Gastric Mucosa/metabolism , Glutathione/metabolism , HSP70 Heat-Shock Proteins/metabolism , Helicobacter pylori/drug effects , Lipid Peroxidation/drug effects , Male , Malondialdehyde/metabolism , Mucus/drug effects , Rats, Sprague-Dawley , Stomach Ulcer/chemically induced , Stomach Ulcer/pathology , Superoxide Dismutase/metabolism
3.
Drug Des Devel Ther ; 10: 297-313, 2016.
Article in English | MEDLINE | ID: mdl-26834460

ABSTRACT

PURPOSE: ß-Mangostin (BM) from Cratoxylum arborescens demonstrated various pharmacological activities such as anticancer and anti-inflammatory. In this study, we aimed to investigate its antiulcer activity against ethanol ulcer model in rats. MATERIALS AND METHODS: BM was isolated from C. arborescens. Gastric acid output, ulcer index, gross evaluation, mucus production, histological evaluation using hematoxylin and eosin and periodic acid-Schiff staining and immunohistochemical localization for heat shock protein 70 (HSP70) and Bax proteins were investigated. Possible involvement of reduced glutathione, lipid peroxidation, prostaglandin E2, antioxidant enzymes, superoxide dismutase and catalase enzymes, radical scavenging, nonprotein sulfhydryl compounds, and anti-Helicobacter pylori were investigated. RESULTS: BM showed antisecretory activity against the pylorus ligature model. The pretreatment with BM protect gastric mucosa from ethanol damaging effect as seen by the improved gross and histological appearance. BM significantly reduced the ulcer area formation, the submucosal edema, and the leukocytes infiltration compared to the ulcer control. The compound showed intense periodic acid-Schiff staining to the gastric mucus layer and marked amount of alcian blue binding to free gastric mucus. BM significantly increased the gastric homogenate content of prostaglandin E2 glutathione, superoxide dismutase, catalase, and nonprotein sulfhydryl compounds. The compound inhibited the lipid peroxidation revealed by the reduced gastric content of malondialdehyde. Moreover, BM upregulate HSP70 expression and downregulate Bax expression. Furthermore, the compound showed interesting anti-H. pylori activity. CONCLUSION: Thus, it could be concluded that BM possesses gastroprotective activity, which could be attributed to the antisecretory, mucus production, antioxidant, HSP70, antiapoptotic, and anti-H. pylori mechanisms.


Subject(s)
Clusiaceae/chemistry , Helicobacter pylori/drug effects , Stomach Ulcer/drug therapy , Xanthones/pharmacology , Animals , Anti-Ulcer Agents/isolation & purification , Anti-Ulcer Agents/pharmacology , Apoptosis/drug effects , Disease Models, Animal , Down-Regulation/drug effects , Ethanol/toxicity , Female , Gastric Mucosa/drug effects , Gastric Mucosa/pathology , HSP70 Heat-Shock Proteins/genetics , Lipid Peroxidation/drug effects , Male , Malondialdehyde/metabolism , Rats , Rats, Sprague-Dawley , Stomach Ulcer/pathology , Up-Regulation/drug effects , Xanthones/isolation & purification , bcl-2-Associated X Protein/genetics
4.
PLoS One ; 10(3): e0121060, 2015.
Article in English | MEDLINE | ID: mdl-25798602

ABSTRACT

BACKGROUND: Zingiber zerumbet Smith is a perennial herb, broadly distributed in many tropical areas. In Malaysia, it's locally known among the Malay people as "lempoyang" and its rhizomes, particularly, is widely used in traditional medicine for the treatment of peptic ulcer disease beyond other gastric disorders. AIM OF THE STUDY: The aim of the current study is to evaluate the gastroprotective effect of zerumbone, the main bioactive compound of Zingiber zerumbet rhizome, against ethanol-induced gastric ulcer model in rats. MATERIALS AND METHODS: Rats were pre-treated with zerumbone and subsequently exposed to acute gastric ulcer induced by absolute ethanol administration. Following treatment, gastric juice acidity, ulcer index, mucus content, histological analysis (HE and PAS), immunohistochemical localization for HSP-70, prostaglandin E2 synthesis (PGE2), non-protein sulfhydryl gastric content (NP-SH), reduced glutathione level (GSH), and malondialdehyde level (MDA) were evaluated in ethanol-induced ulcer in vivo. Ferric reducing antioxidant power assay (FRAP) and anti-H. pylori activity were investigated in vitro. RESULTS: The results showed that the intragastric administration of zerumbone protected the gastric mucosa from the aggressive effect of ethanol-induced gastric ulcer, coincided with reduced submucosal edema and leukocyte infiltration. This observed gastroprotective effect of zerumbone was accompanied with a significant (p <0.05) effect of the compound to restore the lowered NP-SH and GSH levels, and to reduce the elevated MDA level into the gastric homogenate. Moreover, the compound induced HSP-70 up-regulation into the gastric tissue. Furthermore, zerumbone significantly (p <0.05) enhanced mucus production, showed intense PAS stain and maintained PG content near to the normal level. The compound exhibited antisecretory activity and an interesting minimum inhibitory concentration (MIC) against H. pylori strain. CONCLUSION: The results of the present study revealed that zerumbone promotes ulcer protection, which might be attributed to the maintenance of mucus integrity, antioxidant activity, and HSP-70 induction. Zerumbone also exhibited antibacterial action against H. pylori.


Subject(s)
Antioxidants/administration & dosage , Helicobacter pylori/drug effects , Sesquiterpenes/administration & dosage , Stomach Ulcer/prevention & control , Zingiberaceae/chemistry , Animals , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/pharmacology , Antioxidants/pharmacology , Ethanol , Gastric Juice/drug effects , Glutathione/metabolism , Male , Malondialdehyde/metabolism , Plant Extracts/chemistry , Plant Extracts/pharmacology , Rats , Sesquiterpenes/pharmacology , Stomach Ulcer/chemically induced , Stomach Ulcer/metabolism
5.
BMC Complement Altern Med ; 13: 183, 2013 Jul 19.
Article in English | MEDLINE | ID: mdl-23866830

ABSTRACT

BACKGROUND: Mitrella kentii (M. kentii) (Bl.) Miq, is a tree-climbing liana that belongs to the family Annonaceae. The plant is rich with isoquinoline alkaloids, terpenylated dihydrochalcones and benzoic acids and has been reported to possess anti-inflammatory activity. The purpose of this study is to assess the gastroprotective effects of desmosdumotin C (DES), a new isolated bioactive compound from M. kentii, on gastric ulcer models in rats. METHODS: DES was isolated from the bark of M. kentii. Experimental rats were orally pretreated with 5, 10 and 20 mg/kg of the isolated compound and were subsequently subjected to absolute ethanol-induced acute gastric ulcer. Gross evaluation, mucus content, gastric acidity and histological gastric lesions were assessed in vivo. The effects of DES on the anti-oxidant system, non-protein sulfhydryl (NP-SH) content, nitric oxide (NO)level, cyclooxygenase-2 (COX-2) enzyme activity, bcl-2-associated X (Bax) protein expression and Helicabacter pylori (H pylori) were also investigated. RESULTS: DES pre-treatment at the administered doses significantly attenuated ethanol-induced gastric ulcer; this was observed by decreased gastric ulcer area, reduced or absence of edema and leucocytes infiltration compared to the ulcer control group. It was found that DES maintained glutathione (GSH) level, decreased malondialdehyde (MDA) level, increased NP-SH content and NO level and inhibited COX-2 activity. The compound up regulated heat shock protein-70 (HSP-70) and down regulated Bax protein expression in the ulcerated tissue. DES showed interesting anti-H pylori effects. The efficacy of DES was accomplished safely without any signs of toxicity. CONCLUSIONS: The current study reveals that DES demonstrated gastroprotective effects which could be attributed to its antioxidant effect, activation of HSP-70 protein, intervention with COX-2 inflammatory pathway and potent anti H pylori effect.


Subject(s)
Alkenes/therapeutic use , Annonaceae/chemistry , Anti-Ulcer Agents/therapeutic use , Ethanol/adverse effects , Gastric Mucosa/drug effects , Ketones/therapeutic use , Phytotherapy , Stomach Ulcer/drug therapy , Alkenes/isolation & purification , Alkenes/pharmacology , Animals , Anti-Ulcer Agents/pharmacology , Antioxidants/pharmacology , Antioxidants/therapeutic use , Cyclooxygenase 2/metabolism , Disease Models, Animal , Gastric Mucosa/metabolism , Gastric Mucosa/microbiology , Gastric Mucosa/pathology , Glutathione/metabolism , HSP70 Heat-Shock Proteins/metabolism , Helicobacter Infections/drug therapy , Helicobacter Infections/metabolism , Helicobacter Infections/microbiology , Helicobacter Infections/pathology , Helicobacter pylori/drug effects , Hemorrhage/prevention & control , Ketones/isolation & purification , Ketones/pharmacology , Male , Malondialdehyde/metabolism , Nitric Oxide/metabolism , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Rats , Stomach Ulcer/metabolism , Stomach Ulcer/microbiology , Stomach Ulcer/pathology , Sulfhydryl Compounds/metabolism , bcl-2-Associated X Protein/metabolism
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