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1.
Molecules ; 25(18)2020 Sep 15.
Article in English | MEDLINE | ID: mdl-32942704

ABSTRACT

Cyperus has been commonly used as a multi-use medicinal plant in folk medicine worldwide. The objectives of our study were to determine the different metabolites in the Cyperus conglomeratus Rottb. methanol extract, and to assess its in vivo gastroprotective effect in ethanol-induced gastric ulcer model in rats. Serum levels of galactin-3 and TNF-α were employed as biochemical markers. To pinpoint for active agents, comprehensive metabolites profiling of extract via UPLC-qTOF-MS/MS was employed. A total of 77 chromatographic peaks were detected, of which 70 were annotated. The detected metabolites were categorized into phenolic acids and their derivatives, flavonoids, stilbenes, aurones, quinones, terpenes, and steroids. Rats were divided into six groups; healthy control, ulcer control, standard drug group, and 25, 50, 100 mg/kg of C. conglomeratus treated rats. Pre-treatment with C. conglomeratus alcohol extract significantly reduced galactin-3, and TNF-α in ethanol-induced ulcer model at 25, 50, and 100 mg/kg. Further histopathological and histochemical studies revealed moderate erosion of superficial epithelium, few infiltrated inflammatory cells, and depletion of gastric tissue glycoprotein in the ulcer group. Treatment with the extract protected the gastric epithelial cells in a dose-dependent manner. It could be concluded that C. conglomeratus extract provides significant gastroprotective activity in ethanol-induced gastric ulcer and ought to be included in nutraceuticals in the future for ulcer treatment.


Subject(s)
Anti-Ulcer Agents/chemistry , Cyperus/chemistry , Phytochemicals/chemistry , Plant Extracts/chemistry , Administration, Oral , Animals , Anti-Ulcer Agents/pharmacology , Anti-Ulcer Agents/therapeutic use , Chromatography, High Pressure Liquid , Cyperus/metabolism , Ethanol/toxicity , Female , Galectin 3/blood , Gastric Mucosa/drug effects , Gastric Mucosa/pathology , Phytochemicals/pharmacology , Phytochemicals/therapeutic use , Plant Components, Aerial/chemistry , Plant Components, Aerial/metabolism , Ranitidine/therapeutic use , Rats , Rats, Wistar , Stomach Ulcer/chemically induced , Stomach Ulcer/drug therapy , Stomach Ulcer/pathology , Tandem Mass Spectrometry , Tumor Necrosis Factor-alpha/blood
2.
Biomolecules ; 11(8)2021 08 21.
Article in English | MEDLINE | ID: mdl-34439913

ABSTRACT

Different species belonging to the genus Nephthea (Acyonaceae) are a rich resource for bioactive secondary metabolites. The literature reveals that the gastroprotective effects of marine secondary metabolites have not been comprehensively studied in vivo. Hence, the present investigation aimed to examine and determine the anti-ulcer activity of 4α,24-dimethyl-5α-cholest-8ß,18-dihydroxy,22E-en-3ß-ol (ST-1) isolated from samples of a Nephthea species. This in vivo study was supported by in silico molecular docking and protein-protein interaction techniques. Oral administration of ST-1 reduced rat stomach ulcers with a concurrent increase in gastric mucosa. Molecular docking calculations against the H+/K+-ATPase transporter showed a higher binding affinity of ST-1, with a docking score value of -9.9 kcal/mol and a pKi value of 59.7 nM, compared to ranitidine (a commercial proton pump inhibitor, which gave values of -6.2 kcal/mol and 27.9 µM, respectively). The combined PEA-reactome analysis results revealed promising evidence of ST-1 potency as an anti-ulcer compound through significant modulation of the gene set controlling the PI3K signaling pathway, which subsequently plays a crucial role in signaling regarding epithelialization and tissue regeneration, tissue repairing and tissue remodeling. These results indicate a probable protective role for ST-1 against ethanol-induced gastric ulcers.


Subject(s)
Anthozoa/metabolism , Anti-Ulcer Agents/pharmacology , Sterols/chemistry , Animals , Computer Simulation , Ethanol/metabolism , Female , Gastric Mucosa/drug effects , Glycoproteins/metabolism , Inflammation , Magnetic Resonance Spectroscopy , Molecular Docking Simulation , Phosphatidylinositol 3-Kinases/metabolism , Protein Interaction Mapping , Rats , Rats, Wistar , Signal Transduction , Stomach Ulcer/metabolism , Ulcer/metabolism
3.
World J Gastroenterol ; 13(5): 785-90, 2007 Feb 07.
Article in English | MEDLINE | ID: mdl-17278204

ABSTRACT

AIM: To investigate the association between serum insulin-like growth factor 1 (IGF-1), osteocalcin, and parathyroid hormone (PTH) levels with the etiology and clinical condition of patients with chronic liver disease. METHODS: Eighty children with hepatocellular damage were divided into 3 groups according to the etiology of disease infection: bilharziasis (9 patients), hepatitis B virus (HBV, 12 patients) and hepatitis C virus (HCV, 29 patients). The Child score index was found as A in 24 patients, B in 22 patients, C in 4 patients. Thirty healthy children served as control group. HBsAg, HBcAbIgM, HBcAbIgG, and anti-HCV were detected using ELISA technique. HCV-RNA was measured by reverse transcription polymerase chain reaction (RT-PCR). Anti-bilharzial antibodies were detected by indirect haem- agglutination test. Liver function tests were performed using autoanalyser. Serum IGF-1, osteocalcin and PTH levels were measured by ELISA technique. Abdominal ultrasonography was also conducted. RESULTS: Serum IGF-1 level was significantly lower in all patient groups with liver diseases, while serum osteocalcin and PTH levels were significantly elevated in patients with HBV and HCV infections compared with the control group. Serum osteocalcin and PTH concentrations were measured with the severity of liver disease from Child A to C. Child A patients unexpectedly showed significantly reduced IGF-1 levels in comparison to patients staged as Child B or C. Serum osteocalcin level was negatively correlated with albumin (14.7 +/- 0.54 vs 3.6 +/- 0.10, P < 0.05), while that for PTH was positively correlated with total protein (70.1 +/- 2.17 vs 6.7 +/- 0.10, P < 0.05) in patients with HCV infection. CONCLUSION: Low serum IGF-1 level seems to play a critical role in the bone loss in patients with chronic liver disease. Elevated biochemical markers of bone remodeling suggest high-turnover in patients with viral infection and reflect severity of the clinical stage.


Subject(s)
Biomarkers/blood , Liver Diseases/blood , Liver Diseases/complications , Osteoporosis/blood , Osteoporosis/etiology , Adolescent , Child , Child, Preschool , Chronic Disease , Egypt , Female , Humans , Insulin-Like Growth Factor I/metabolism , Male , Osteocalcin/blood , Parathyroid Hormone/blood
4.
Pak J Biol Sci ; 10(17): 2809-16, 2007 Sep 01.
Article in English | MEDLINE | ID: mdl-19090181

ABSTRACT

Heavy metals are widely distributed in the environment and some of them occur in food, water, air and tissues even in the absence of occupational exposure. Among of these lead, (Pb) is a hazardous substance to human and animals. The present study was carried out to investigate the possible protective effect of co-administered Nigella sativa seeds on lead acetate-induced rats' toxicity in particularly on liver and kidney. Thirty-six male rats were divided into six groups, 6 rats each. The first group was served as a control, while the second group was fed on the basal diet with Nigella sativa addition, whereas the other groups contained lead acetate (10 and 20% of LD50) with and without Nigella sativa supplementation for six weeks. At the end of the feeding period, rats were fasted over night and anesthetized and blood and tissue samples were taken for biochemical and histopathological studies. The results of this study revealed that lead acetate caused significant elevations in AST, urea, creatinine, total cholesterol and triglycerides in serum. Lead treatment also produced significant decrease in serum total protein and albumin. Histopathological observations showed severe damage in the liver and kidneys. Its damaged areas were measured using Image analyzer. Combined treatment of lead-exposed animals with Nigella sativa showed marked improvement in both biochemical and histopathological findings as well as reduction in the damaged areas. These experimental results strongly indicate the protective effect of Nigella sativa against toxic effect of lead on liver and kidney tissues.


Subject(s)
Liver/drug effects , Nigella sativa/metabolism , Organometallic Compounds/toxicity , Plant Extracts/pharmacology , Seeds/metabolism , Animal Feed , Animals , Kidney/drug effects , Liver/pathology , Male , Plants, Medicinal/metabolism , Rats , Rats, Sprague-Dawley , Time Factors
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