18 results on '"Khushtar M"'
Search Results
2. Protective effect of ginger oil on aspirin and pylorus ligation-induced gastric ulcer model in rats
- Author
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Bhandari, Uma, primary, Khushtar, M, additional, Kumar, V, additional, and Javed, K, additional
- Published
- 2009
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3. Protective Effect of Ginger oil on Aspirin and Pylorus Ligation-Induced Gastric Ulcer model in Rats.
- Author
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KHUSHTAR, M., KUMAR, V., JAVED, K., and BHANDARI, UMA
- Subjects
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ASPIRIN , *LABORATORY rats , *ULCERS , *MUCUS , *PEPTIC ulcer - Abstract
The present investigation was performed in aspirin and pylorus ligation-induced ulcer model in Wistar rats, in which ability of ginger oil to provide gastric protection was studied at two different doses, 0.5 and 1 g/kg po. Gastric protection was evaluated by measuring the ulcer index, serum γ-GTP levels, total acidity of gastric juice and gastric wall mucus thickness. The results obtained in the present study indicated that ginger oil has a protective action against gastric ulcers induced by aspirin plus pylorus ligation in Wistar rats. [ABSTRACT FROM AUTHOR]
- Published
- 2009
4. Phytochemical Estimation and Therapeutic Amelioration of Aesculus hippocastanum L. Seeds Ethanolic Extract in Gastric Ulcer in Rats Possibly by Inhibiting Prostaglandin Synthesis.
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Idris S, Mishra A, and Khushtar M
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- Rats, Animals, Antioxidants pharmacology, Antioxidants therapeutic use, Ranitidine adverse effects, Ulcer drug therapy, Quercetin, Plant Extracts pharmacology, Plant Extracts therapeutic use, Plant Extracts chemistry, Indomethacin therapeutic use, Glutathione, Superoxide Dismutase, Rutin adverse effects, Prostaglandins adverse effects, Phytochemicals therapeutic use, Stomach Ulcer chemically induced, Stomach Ulcer drug therapy, Stomach Ulcer pathology, Aesculus
- Abstract
Objective: To quantify phytochemicals using liquid chromatography and mass spectroscopy (LCMS) analysis and explore the therapeutic effect of Aesculus hippocastanum L. (AH) seeds ethanolic extract against gastric ulcers in rats., Methods: Preliminary phytochemical testing and LCMS analysis were performed according to standard methods. For treatment, the animals were divided into 7 groups including normal control, ulcer control, self-healing, AH seeds low and high doses, ranitidine and per se groups. Rats were orally administered with 10 mg/kg of indomethacin, excluding the normal control group (which received 1% carboxy methyl cellulose) and the per se group (received 200 mg/kg AH seeds extract). The test group rats were then given 2 doses of AH seeds extract (100 and 200 mg/kg, respectively), while the standard group was given ranitidine (50 mg/kg). On the 11th day, rats in all groups were sacrificed, and their stomach was isolated to calculate the ulcer index, and other parameters such as blood prostaglandin (PGE
2 ), tissue superoxide dismutase (SOD), catalase (CAT), malonyldialdehyde (MDA), and glutathione (GSH). All isolated stomach tissues were analyzed for histopathological findings., Results: The phytochemical examination shows that the AH seeds contain alkaloids, flavonoids, saponins, phenolic components, and glycosides. LCMS analysis confirms the presence of quercetin and rutin. The AH seeds extract showed significant improvement in gastric mucosa conditions after indomethacin-induced gastric lesions (P<0.01). Further marked improvement in blood PGE2 and antioxidant enzymes, SOD, CAT, MDA and GSH, were observed compared with self-healing and untreated ulcer-induced groups (P<0.01). Histopathology results confirmed that AH seeds extract improved the mucosal layer and gastric epithelial membrane in treated groups compared to untreated ulcer-induced groups., Conclusions: LCMS report confirms the presence of quercetin and rutin in AH seeds ethanolic extract. The therapeutic effect of AH seeds extract against indomethacin-induced ulcer in rat model indicated the regenerated membrane integrity, with improved cellular functions and mucus thickness. Further, improved antioxidant enzyme level would help to reduce PGE2 biosynthesis., (© 2023. The Chinese Journal of Integrated Traditional and Western Medicine Press and Springer-Verlag GmbH Germany, part of Springer Nature.)- Published
- 2023
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5. Neuroinflammation: A Potential Risk for Dementia.
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Ahmad MA, Kareem O, Khushtar M, Akbar M, Haque MR, Iqubal A, Haider MF, Pottoo FH, Abdulla FS, Al-Haidar MB, and Alhajri N
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- Animals, Cognitive Dysfunction diagnosis, Humans, Inflammation Mediators metabolism, Risk Factors, Dementia etiology, Inflammation complications, Nervous System pathology
- Abstract
Dementia is a neurodegenerative condition that is considered a major factor contributing to cognitive decline that reduces independent function. Pathophysiological pathways are not well defined for neurodegenerative diseases such as dementia; however, published evidence has shown the role of numerous inflammatory processes in the brain contributing toward their pathology. Microglia of the central nervous system (CNS) are the principal components of the brain's immune defence system and can detect harmful or external pathogens. When stimulated, the cells trigger neuroinflammatory responses by releasing proinflammatory chemokines, cytokines, reactive oxygen species, and nitrogen species in order to preserve the cell's microenvironment. These proinflammatory markers include cytokines such as IL-1, IL-6, and TNFα chemokines such as CCR3 and CCL2 and CCR5. Microglial cells may produce a prolonged inflammatory response that, in some circumstances, is indicated in the promotion of neurodegenerative diseases. The present review is focused on the involvement of microglial cell activation throughout neurodegenerative conditions and the link between neuroinflammatory processes and dementia.
- Published
- 2022
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6. Gastroprotective effect of Hyssopus officinalis L. leaves via reduction of oxidative stress in indomethacin-induced gastric ulcer in experimental rats.
- Author
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Tahir M, Rahman MA, and Khushtar M
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- Animals, Gastric Mucosa, Hyssopus Plant, Indomethacin toxicity, Oxidative Stress, Plant Extracts metabolism, Plant Extracts pharmacology, Plant Leaves, Rats, Rats, Sprague-Dawley, Rats, Wistar, Stomach Ulcer chemically induced, Stomach Ulcer drug therapy, Stomach Ulcer prevention & control
- Abstract
Peptic ulcer disease (PUD) is an important cause of morbidity and mortality throughout the world affecting lives of millions of people. Hyssopus officinalis L. have been used as carminative and antispasmodic stomachic in Iran and Indian traditional systems of medicine. Thus, present study was aimed to evaluate gastroprotective activity of ethanolic extract of Hyssopus officinalis L. leaves (EEHO) in indomethacin-induced gastric ulcer in experimental rats. Female Sprague Dawley rats of groups I, II, III, IV, V, and VI received orally 1 mL/kg/day 1% CMC (carboxy methylcellulose), 1 mL/kg/day 1% CMC, 250 mg EEHO/kg/day, 500 mg EEHO/kg/day, 50 mg ranitidine/kg/day and 500 mg EEHO/kg/day respectively for 10 days. Then, all the groups except groups I and VI were orally administered with 20 mg indomethacin/kg b.wt on 11th day. Ulcer index and mucus barrier were determined. Antioxidant parameters thiobarbituric acid reactive substances (TBARS), glutathione-reduced (GSH), catalase and superoxide dismutase (SOD) were evaluated. Stomach was examined for histopathology also. EEHO in groups III and IV significantly ( p < 0.01) increased the mucus barrier, SOD, GSH, and catalase while significantly ( p < 0.01) decreased the ulcer index and TBARS as compared to ulcer control group II. Histopathological findings showed that indomethacin administration in group II caused PUD (gastric ulcer) and the gastric ulcer was protected by pretreatment with EEHO in groups III and IV. Thus, EEHO possesses gastroprotective activity where the gastroprotection is by strengthening of the gastric mucosa and reduction of oxidative stress. The gastroprotective activity of EEHO was comparable to that of standard drug ranitidine.
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- 2022
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7. Recent Therapeutic Interventions of Fenugreek Seed: A Mechanistic Approach.
- Author
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Idris S, Mishra A, and Khushtar M
- Subjects
- Anti-Infective Agents chemistry, Anti-Infective Agents pharmacology, Anti-Infective Agents therapeutic use, Anti-Inflammatory Agents chemistry, Anti-Inflammatory Agents pharmacology, Anti-Inflammatory Agents therapeutic use, Anti-Obesity Agents chemistry, Anti-Obesity Agents pharmacology, Anti-Obesity Agents therapeutic use, Antineoplastic Agents chemistry, Antineoplastic Agents pharmacology, Antineoplastic Agents therapeutic use, Antioxidants chemistry, Antioxidants pharmacology, Antioxidants therapeutic use, Bone Density Conservation Agents chemistry, Bone Density Conservation Agents pharmacology, Bone Density Conservation Agents therapeutic use, Humans, Hypoglycemic Agents chemistry, Hypoglycemic Agents pharmacology, Hypoglycemic Agents therapeutic use, Medicine, Arabic methods, Medicine, Ayurvedic methods, Medicine, Unani methods, Plant Extracts chemistry, Plant Extracts therapeutic use, Protective Agents chemistry, Protective Agents pharmacology, Protective Agents therapeutic use, Phytotherapy methods, Plant Extracts pharmacology, Seeds chemistry, Trigonella chemistry
- Abstract
Fenugreek seeds have widespread relations with Ayurveda, Unani, and Arabic medicine. The seeds were useful for the treatment and prevention of different ailments. Fenugreek ( Trigonella foenum-graecum ) or methi is from the Leguminosae family and are primarily known for its anti-diabetic and hypocholesterolemic activities. The germinated fenugreek seeds were used in the treatment of E.coli infection in Germany and France. The important phytoconstituents responsible for such medicinal applications are saponins, polyunsaturated fatty acids, galactomannans, trigonelline , and 4-hydroxy isoleucine. Flavonoids, apigenin 6,8-di-C-glucoside, apigenin-6-C-glucosyl-8-C-galactoside, 6-Cgalactosyl- 8-C-arabinoside are the chief ingredients of fenugreek seeds; responsible for reducing blood glucose while given to diabetic rats, whereas important flavones are epigenin, luteolin and vitexin. The other major bioactive components in fenugreek seeds are polyphenols like rhaponticin and isovitexin. Fenugreek seeds contain phosphorus and are categorized into different classes such as inorganic phosphorus, phospholipids, phytates, phosphor-proteins, and nucleic acid. Germinated seeds profusely filled with amino acids with amino acids, proteins, ascorbic acid, sugars. Further, this review shares information about the recent therapeutic intervention not covered earlier; on in vivo and in vitro and some clinical applications against certain interesting ailments other than older applications. This review includes certain nano delivery systems of Fenugreek seeds and their medicinal application., Competing Interests: The authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this article., (Thieme. All rights reserved.)
- Published
- 2021
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8. A Comprehensive Review on Physiological Effects of Curcumin.
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Ahsan R, Arshad M, Khushtar M, Ahmad MA, Muazzam M, Akhter MS, Gupta G, and Muzahid M
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- Alzheimer Disease drug therapy, Animals, Curcumin pharmacology, Disease Models, Animal, Heart Diseases drug therapy, Humans, Liver Diseases drug therapy, Lung Neoplasms drug therapy, Osteoarthritis drug therapy, Curcuma chemistry, Curcumin therapeutic use, Medicine, Ayurvedic methods, Phytotherapy methods
- Abstract
Turmeric ( Curcuma longa Linn) is an herbal medicine which is traditionally used as a spice, food colouring or flavouring agent and widely used for several diseases such as biliary disorders, cough, hepatic disorders, rheumatism, wound healing, sinusitis, diabetes, cardiac disorders and neurological disorder. It belongs to the Zingiberaceae family. Turmeric is a popular domicile remedy used in Indian food, is mainly a native of south-east Asia, is widely cultivated in India, Sri Lanka, Indonesia, China, Jamaica , Peru, Haiti and Taiwan and it is very less expensive. Curcumin is the main principle of turmeric. Curcumin has shown various biological properties pre-clinically and clinically. Curcumin is a highly pleiotropic molecule which can be modulators of various intracellular signalling pathways that maintain cell growth. It has been reported as anti-inflammatory, anti-angiogenic, antioxidant, wound healing, anti-cancer, anti-Alzheimer and anti-arthritis and possesses an excellent safety profile. All previous review articles on curcumin have collected the biological/pharmacological activities but this review article summarises the most interesting in vitro and in vivo studies of curcumin on most running diseases around the whole world., Competing Interests: The authors declare that they have no conflict of interest to disclose., (Thieme. All rights reserved.)
- Published
- 2020
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9. Current Pharmacological Trends on Myricetin.
- Author
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Gupta G, Siddiqui MA, Khan MM, Ajmal M, Ahsan R, Rahaman MA, Ahmad MA, Arshad M, and Khushtar M
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- Alzheimer Disease drug therapy, Animals, Diabetes Mellitus drug therapy, Disease Models, Animal, Epilepsy drug therapy, Flavonoids chemistry, Flavonoids isolation & purification, Flavonoids pharmacology, Heart Diseases prevention & control, Humans, Inflammation drug therapy, Liver Diseases prevention & control, Neoplasms drug therapy, Osteoporosis drug therapy, Solubility, Flavonoids therapeutic use, Plants, Medicinal chemistry
- Abstract
Myricetin is a member of the group of flavonoids called flavonols. Myricetin is obtained from various fruit, vegetables, tea, berries and red wine. Myricetin is characterized by the pysrogallol B-ring, and the more hydroxylated structure is known to be capable for its increased biological properties compared with other flavonols. Myricetin is produced by the Myricaceae, Anacardiaceae, Polygonaceae, Pinaceae and Primulacea families. It is soluble in organic solvent such as ethanol, DMSO (dimethyl sulfoxide), and dimethyl formamide (DMF). It is sparingly soluble in aqueous buffers. Myricetin shows its various pharmacological activities including antioxidant, anti-amyloidogenic, antibacterial, antiviral, antidiabetic, anticancer, anti-inflammatory, anti-epileptic and anti-ulcer. This review article focuses on pharmacological effects of Myricetin on different diseases such as osteoporotic disorder, anti-inflammatory disorder, alzheimer's disease, anti-epileptic, cancer, cardiac disorder, diabetic metabolic disorder, hepatoprotective disorder and gastro protective disorder., Competing Interests: The author(s) declare(s) that they have no conflict of interest to disclose., (Thieme. All rights reserved.)
- Published
- 2020
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10. Phytochemical, ethanomedicinal and pharmacological applications of escin from Aesculus hippocastanum L. towards future medicine.
- Author
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Idris S, Mishra A, and Khushtar M
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- Animals, Drug Delivery Systems, Escin administration & dosage, Escin isolation & purification, Humans, Plant Extracts administration & dosage, Plant Extracts chemistry, Seeds, Aesculus chemistry, Escin pharmacology, Plant Extracts pharmacology
- Abstract
Medicinal plants are used from ancient times for treatment of various ailments. Aesculus hippocastanum (Horse chestnut), is the popular and most valuable tree native to the South East Europe. It's seed extracts and their concentrates contain phytocompounds like flavonoids, polyphenols, triterpenoid saponin glycosides (escin), epicatechin, tannins, kaempferol, esculin, fraxin, carbohydrate, essential fatty acids (linoleic acid), oleic acid and purine bases (adenine and guanine). Due to these vital phyto-constituents, horse chestnut is used in phytomedicine for the prevention and treatment of diverse disorders as in venous congestion in leg ulcers, bruises, arthritis, rheumatism, diarrhoea, phlebitis etc. We collected the pharmacological applications of Aesculus hippocastanum L. extracts and escin as the cheif bioactive compound and their uses in traditionally and clinically for the management of various disorders. This review describes the efficacy of A. hippocastanum L. extracts and their bioactive compounds. So in the furtue this plant may be useful for the alternative treatment measure for various ailments via incorporating either extract or escin into novel delivery systems for improving the social health in future and would provide improved quality of life.
- Published
- 2020
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11. A Phytochemical and Ethnopharmacological Recapitulation on Hamelia patens.
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Noor G, Ahmad MA, Ahsan F, Mahmood T, Arif M, and Khushtar M
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- Flavonoids pharmacology, Humans, Oxindoles pharmacology, Phenols pharmacology, Plant Extracts chemistry, Plant Extracts therapeutic use, Ethnopharmacology methods, Hamelia chemistry, Plant Extracts pharmacology
- Abstract
The world health organization reports that 80% of the population living within the developing countries depends basically on traditional medicine for his or her primary health care. Quite half the entire world's population still depends entirely on plants for medicines, and plants provides the active ingredients to the most traditional medical products. Hamelia patens that belong to the family Rubiaceae, is mainly found in tropical and sub-tropical areas. It is used in folk medicine against a wide range of diseases such as athlete's foot, skin problems, insect sting, psychiatric disorder, rheumatism, headache, asthma, dysentery, menses, ovarian and uterine disorders. Hamelia consists of an important bioactive constituent such as oxindole alkaloids, flavonoids, and phenolic content. Due to the presence of chlorogenic acid and epicatechin constituent in the methanolic extract of Hamelia patens , there is a noticeable anti-hyperglycemic activity as well as it possesses antioxidant activity. Acute and sub-acute toxicity study has been performed on Hamelia patens which shows that it is safe and can be used for humans. Against fungi and bacteria, the ethanol leaf extract of Hamelia has a maximum inhibitory effect. The plant has various therapeutic effects like anti-inflammatory, analgesic, anti-diarrheal, anthelmintic, antidepressant, hepatoprotective, antiurolithiatic, diuretic, wound healing, and many others. In this article, we have discussed chemical constituent, pharmacological activity and traditional use of Hamelia patens., Competing Interests: The authors report no conflicts of interest., (© Georg Thieme Verlag KG Stuttgart · New York.)
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- 2020
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12. Guggulipid: A Promising Multi-Purpose Herbal Medicinal Agent.
- Author
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Ahmad MA, Mujeeb M, Akhtar M, Khushtar M, Arif M, and Haque MR
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- Acne Vulgaris drug therapy, Arthritis drug therapy, Commiphora, Epilepsy drug therapy, Humans, Inflammation drug therapy, Lipid Metabolism Disorders drug therapy, Liver Diseases drug therapy, Obesity drug therapy, Pain drug therapy, Peptic Ulcer drug therapy, Plant Extracts chemistry, Plant Extracts pharmacology, Plant Gums chemistry, Plant Gums pharmacology, Pregnenediones chemistry, Stereoisomerism, Plant Extracts therapeutic use, Plant Gums therapeutic use, Pregnenediones pharmacology
- Abstract
Herbal medicines therapy is appreciated by many research works because herbal drugs have relatively high therapeutic window, lower side effects and more cost effective. Guggulipid is an ethyl acetate extract of resin known as guggul from the tree Commiphora wightii / mukul (Arn.) Bhandari . Chemical analysis revealed that the compounds responsible for the major activities of gum guggul are the isomers E- and Z-guggulsterone. Guggul has been used for thousands of years in the treatment of arthritis, inflammation, obesity, cardiac protection, anti-ulcer, anti-epileptic and disorders of lipid metabolism. This review is an assortment of available information reported on its chemical, pharmacological and toxicological properties in various research studies. The available therapeutic properties of guggulipid make it suitable natural product for the treatment of various disorders like inflammation, pain, wounds, liver disorder and Acne etc. Graphical Abstract Graphical Abstract., Competing Interests: The author has no conflict of interest., (© Georg Thieme Verlag KG Stuttgart · New York.)
- Published
- 2020
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13. Quality Control Standardization and Evaluation of Antimicrobial Potential of Daruhaldi ( Berberis aristata DC) Stem Bark.
- Author
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Khan MI, Rahman MA, Khalid M, Khushtar M, and Mujahid M
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- Aspergillus drug effects, Bacillus subtilis drug effects, Berberine analysis, Berberine pharmacology, Chromatography, High Pressure Liquid, Escherichia coli drug effects, Flavonoids analysis, Flavonoids pharmacology, Humans, Penicillium drug effects, Phenols analysis, Phenols pharmacology, Plant Bark chemistry, Plant Extracts chemistry, Plant Extracts standards, Plant Stems chemistry, Quality Control, Anti-Bacterial Agents pharmacology, Antifungal Agents pharmacology, Bacteria drug effects, Berberis chemistry, Fungi drug effects, Plant Extracts pharmacology
- Abstract
Berberis aristata is used for the treatment of diabetes, piles, and liver diseases. As the drug is broadly used in Indigenous systems of medicine, it was designed to set the quality standards and antimicrobial potential for the stem bark of Berberis aristata . Botanical, physicochemical, pharmacotoxicological, fluorescence, microbial load, and phytochemical parameters of the stem bark were determined. High-performance thin-layer chromatography (HPTLC) was carried out by the CAMAG-HPTLC system. Berberine, total phenolics, and flavonoids were estimated. The antimicrobial potential was determined against the bacteria Bacillus subtilis and Escherichia coli and fungi Penicillium citrinum and Aspergillus terreus . The foreign matter, foaming index, swelling index, bitterness value, resin content, loss on drying, total ash, acid-insoluble ash, water-soluble ash, heavy metals, microbial load, berberine content, total phenolic content, and total flavonoid content were found to be 0, 0, 5, 1.34, 0.86%, 2.07%, 4.33%, 0.28%, 2.66%, within limits, 6 colonies in 1/100 dilution, 0.032 mg/g, 144.04 µg/ml, and 85.61 µg/ml, respectively. Phytochemicals such as phenolics, flavonoids, and sterols were present in the methanolic extract. The fluorescences observed in UV light were of different colors in different solvents. The methanolic extract and standards exhibited antimicrobial activity at the tested concentrations against the microbial strains. Results confirmed the quality and purity of the drug B. aristata . Results also confirmed that methanolic extract of B. aristata stem bark possesses potent antimicrobial activity. Thus, the use of this quality-controlled plant-derived drug with established antimicrobial property could be of great significance in quality-control standardization and preventive and therapeutic approaches to infectious diseases.
- Published
- 2020
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14. Augmented Reversal of Cisplatin-Induced Delayed Gastric Emptying by Amla (Emblica Officinalis) Fruit Extract in Sprague-Dawley Rats.
- Author
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Ahmad A, Khushtar M, Kumar R, Badruddeen, Riyaz A, Khan MI, and Rahman A
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- Animals, Antineoplastic Agents adverse effects, Female, Gastric Emptying drug effects, Male, Phytotherapy, Plant Extracts administration & dosage, Rats, Rats, Sprague-Dawley, Cisplatin adverse effects, Fruit chemistry, Gastroparesis chemically induced, Gastroparesis drug therapy, Phyllanthus emblica, Plant Extracts therapeutic use
- Abstract
Despite the availability of effective antiemetics, control of acute and delayed chemotherapy-induced nausea and vomiting (CINV) is often suboptimal and there is need of an inexpensive and safer alternative. Thus, this study was designed to evaluate the effect of Emblica officinalis Gaertn (Euphorbiaceae) fruit extract (EEEO) on cisplatin-induced delayed gastric emptying in Sprague-Dawley rats so that Emblica officinalis can be clarified for its application in CINV as a potential candidate. Groups I, II, III, IV, and V rats were pretreated orally with 1% carboxymethyl cellulose (CMC, 1 mL/kg), 1% CMC (1 mL/kg), EEEO (250 mg/kg), EEEO (500 mg/kg), and ondansetron (3 mg/kg), respectively, for 5 consecutive days. Then, Group I rats received 0.1 mL of normal saline and Groups II-V rats received 10 mg/kg body weight of cisplatin intraperitoneally. Immediately after that, a test meal (1.5 mL/rat) was administered to each group, and after 30 minutes, rats were euthanized to evaluate the percentage of gastric emptying. EEEO at the specified doses reversed the cisplatin-induced delayed gastric emptying. EEEO (500 mg/kg body weight) pretreatment for 5 days before cisplatin challenge in Group IV rats significantly (p < .05) increased gastric emptying to 74.25% ± 7.19%. Reversal of cisplatin-induced delay in gastric emptying by EEEO (500 mg/kg body weight) in Group IV was significantly (p < .05) comparable to that of the ondansetron treated Group V. EEEO possesses the property to reverse the cisplatin-induced delayed gastric emptying and can be used as an antiemetic for the prevention of CINV.
- Published
- 2018
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15. Effect of Nigella sativa L. seed extract on cisplatin-induced delay in gastric emptying in Sprague-Dawley rats.
- Author
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Riyaz A, Nazir S, Khushtar M, Mishra A, Jahan Y, and Ahmad A
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- Animals, Male, Ondansetron pharmacology, Rats, Rats, Sprague-Dawley, Seeds, Cisplatin pharmacology, Gastric Emptying drug effects, Nigella sativa, Plant Extracts pharmacology
- Abstract
The aim of this study was focused on investigating the possible protective effect of Nigella sativa L. seed extract against cisplatin-induced delay in gastric emptying, in a rat model. Twenty-five male Sprague-Dawley rats were divided into five equal groups as follows: Group I or control group, Group II (cisplatin 10 mg/kg, i.p at day 5), Group III (N. sativa L. 250 mg/kg for 5 days + cisplatin 10 mg/kg, i.p on day 5), Group IV (N. sativa L. 500 mg/kg for 5 days + cisplatin 10 mg/kg, i.p on day 5) and Group V (ondansetron 3 mg/kg/day, per os + cisplatin 10 mg/kg, i.p on day 5). Phenol red meal was adopted to estimate gastric emptying in different groups of the rats. Gastric emptying was significantly increased (p < 0.01) in N. sativa L. seed extract-pretreated rats (Group III and Group IV) when compared to cisplatin treatment alone (Group II). However, ondansetron produced significantly (p < 0.01) better reversal than N. sativa L. seed extract.
- Published
- 2017
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16. Protective effect of hydro-alcoholic extract of Salvia haematodes Wall root on cognitive functions in scopolamine-induced amnesia in rats.
- Author
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Shawwal M, Badruddeen, Khushtar M, and Rahman MA
- Abstract
Diminished cholinergic transmission may be responsible for development of amnesia. Hence, the present study was undertaken to investigate the possible protective effect of hydro-alcoholic extract of Salvia haematodes Wall root (HESH) on cognitive functions in scopolamine-induced amnesia in adult Sprague Dawley rats. The rats were divided randomly into five groups each consisting of five rats ( n = 5 ). Rats of the groups I, II, III, IV, and V received orally normal saline (10 ml/kg b. wt.), normal saline (10 ml/kg), standard drug rivastigmine (1.5 mg/kg), HESH (20 mg/kg), and HESH (40 mg/kg), respectively once a day for fourteen days. Then, they were subjected to single dose of scopolamine (1 mg/kg b. wt. ip ) except in group I on fourteenth day 60 min after respective normal saline or drug administration. They were observed for the effects on step down latency (SDL), locomotor activity and brain AChE activity for the learning and memory. The acquisition SDL, retention SDL and locomotor activity were significantly ( p < 0.01) decreased while AChE activity was significantly ( p < 0.01) increased in scopolamine-treated group II as compared to normal control group I. The acquisition SDL, retention SDL and locomotor activity were significantly ( p < 0.01) increased while, AChE activity was significantly ( p < 0.01) decreased with all the doses of HESH and in rivastigmine-treated group as compared to scopolamine-treated group II. Hydro-alcoholic extract of S haematodes root possesses protective effect on cognitive functions and may prove to be a useful memory restorative agent in the management of cognitive dysfunctions as in amnesia and Alzheimer's diseases.
- Published
- 2017
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17. Hepatoprotective effect of Anacyclus pyrethrum Linn. against antitubercular drug-induced hepatotoxicity in SD rats.
- Author
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Usmani A, Mujahid M, Khushtar M, Siddiqui HH, and Rahman MA
- Subjects
- Alanine Transaminase blood, Alkaline Phosphatase, Animals, Aspartate Aminotransferases blood, Bilirubin blood, Blood Proteins metabolism, Cholesterol blood, L-Lactate Dehydrogenase blood, Liver enzymology, Male, Organ Size, Plant Extracts pharmacology, Plant Extracts therapeutic use, Rats, Sprague-Dawley, Antitubercular Agents adverse effects, Asteraceae, Chemical and Drug Induced Liver Injury prevention & control, Isoniazid adverse effects, Liver drug effects, Phytotherapy, Rifampin adverse effects
- Abstract
Background: Traditional remedies employ herbal drugs for the treatment of liver ailments and hepatoprotection. Thus, the present study was designed to evaluate the hepatoprotective effect of "extract of Anacyclus pyrethrum Linn" (APE) against antitubercular drug-induced hepatotoxicity in rats., Methods: Group I rats (normal control) received vehicle (1 % CMC), while group II rats (hepatotoxic control) isoniazid (INH) plus rifampicin (RIF) each 50 mg/kg/day po, for 28 days. Group III, IV and V rats were administered with APE 200, APE 400 and silymarin 100 mg/kg/day po, respectively, for 28 days. Concurrently, hepatotoxicity was tried to induce by coadministration of INH and RIF each 50 mg/kg/day po for 28 days in group III, IV and V rats. After 24 h of the last dosing, blood was obtained under light anesthesia and the rats were killed. Hepatoprotective effect was assessed by liver weight, relative liver weight and biochemical parameters such as serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase (ALP), lactate dehydrogenase (LDH), serum bilirubin, cholesterol, total protein and albumin levels., Results: Group IV rats showed significant (p<0.01) decrease in SGPT, SGOT, ALP, LDH, cholesterol, serum bilirubin, liver weight and relative liver weight Levels, while significant (p<0.01) increase in final body weight (b. wt.), total protein and albumin levels as compared to group II rats. Hepatoprotective effect of APE 400 mg/kg/day was comparable to that of silymarin 100 mg/kg/day and the hepatic marker levels were also restored. Hepatoprotective effect of APE was well supported by the histopathological results., Conclusions: Hydroalcoholic APE root possesses hepatoprotective activity as it exhibited the protective effect against INH plus RIF-induced hepatotoxicity in rats.
- Published
- 2016
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18. Protective effect of hydro-alcoholic extract of Ruta graveolens Linn. leaves on indomethacin and pylorus ligation-induced gastric ulcer in rats.
- Author
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Tarique M, Siddiqui HH, Khushtar M, and Rahman MA
- Abstract
Background: The search for an ideal and new antiulcer drug has been extended to herbals for novel molecules that decrease the incidence of relapse and afford better protection., Objective: The present study was designed to investigate the protective effect of hydro-alcoholic extract of Ruta graveolens (RGE) Linn. leaves on indomethacin (IND) and pylorus ligation-induced gastric ulcer in Wistar rats., Materials and Methods: The rats of all the six groups were deprived of food for 24 h. Then, the first group received 1 ml/kg/day p.o. of 1% carboxymethylcellulose calcium (CMC), second group 1 ml/kg/day p.o. of 1% CMC and third group 20 mg/kg/day p.o. of IND. Fourth and fifth groups received RGE 200 and 400 mg/kg/day p.o., respectively; while the sixth group 10 mg/kg/day p.o. omeprazole. After 30 min, last three groups received 20 mg/kg/day p.o. of IND also. All these treatments after food deprivation were repeated each day for 5 consecutive days. Pylorus ligation was performed on 6th day in last five groups. After 4 h, stomach by sacrifice of the rats was examined for ulcer index (UI) and gastric mucus. Gastric juice was assessed for acidity, pH and pepsin; while gastric tissues were assessed for thiobarbituric acid reactive substance (TBARS) and glutathione (GSH)., Results: Fifth group showed significant decrease in UI (10.33 ± 0.67), TBARS (0.33 ± 0.03 mmol/mg), free acidity (48.78 ± 5.12 meq/l/100 g), total acidity (99.33 ± 9.31 meq/l/100 g), and pepsin activity (8.47 ± 0.41 μg/ml) levels while it showed significant increase in mucus (412.4 ± 21.6 μg/g), GSH (57.9 ± 4.8 mmol/mg) and pH (3.32 ± 0.27) compared to third group. Percent protection in RGE 400 mg was found to be 63.32 compared to indomethacin., Conclusion: RGE possesses antiulcerogenic activity as it exhibits protective effect on gastric ulcer in rats., (Copyright © 2016 Transdisciplinary University, Bangalore and World Ayurveda Foundation. Published by Elsevier B.V. All rights reserved.)
- Published
- 2016
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