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Showing 3 results for Atorvastatin
Changizi Ashtiyani S , Zarei A, Taheri S, Ramazani M, Volume 17, Issue 2 (7-2015)
Abstract
Background and Objective: Thyroid hormones have a key role in regulation of metabolism and function of the tissues. This study was carried out to evaluate the effect of alcoholic extract of Portulaca Oleracea on serum level of thyroid hormones in hypercholestrolemic rats. Methods: In this experimental study, 60 adult male Wistar rats were randomly allocated into six groups including: control group with normal diet, fat diet group with high fat diet and interventional groups were received high fat diet and alcoholic extract of Portulaca Oleracea with maximum dose (800 mg/kg/bw), moderate dose (400 mg/kg/bw), minimum dose (200 mg/kg/bw) intraperitoneally for 21 days and finally, animals in atorvastatin group were received high fat diet with atorvastatin (10 mg/kg/bw, intraperitoneally) for 21 days. After the end of this period, T3, T4, TSH and total cholesterol measured for each animal. Results:Serum level of T3 and T4 in the experimental groups which were received Portulaca Oleracea extract and atorvastatin group significantly increased in compared to controls (P<0.05). Serum level of TSH level significantly reduced in the experimental groups which were received Portulaca Oleracea extract and atorvastatin group in compared to controls (P<0.05). The serum total cholesterol level significantly reduced in the experimental groups which were received Portulaca Oleracea extract and atorvastatin group in compared to fat diet group (P<0.05). Conclusion: Portulaca Oleracea extract with increasing of secretion of thyroid hormone reduced the total cholesterol and TSH animals with hypercholesterolemia.
Mohammad Nosrati, Hamid Sepehri, Volume 21, Issue 1 (3-2019)
Abstract
Background and Objective: Atorvastatin is a member of the statin family with lipophilic character and anti-hyperlipidemic effect. There is many evidence that atorvastatin has protective effect on cognitive function. This study was done to evaluate the effect of atorvastatin on spatial memory in rats following a high-fat diet.
Methods: This experimental study was performed on 35 male Wistar male rats. Animals were randomly allocated into 5 groups including control, control plus atorvastatin and sham (received high-fat diet for 4 weeks) and high-fat diet plus atorvastatin (10 and 50 mg/kg, for 4 weeks). Learning and spatial memory were measured using Morris water maze for a 6-day period including 5 days training and the last day, test day (probe day).
Results: High-fat diet reduced learning and poor memory performance during training and probe compared to the control group, and also on the probe day, the high-fat group spent less time in the target quarter (P<0.05). Administration of atorvastatin after a high-fat diet improvement spatial memory in compared to high-fat group (P<0.05).
Conclusion: Short-term treatment (4 weeks) with atorvastatin in high-fat dietary rats can improve spatial memory.
Zahra Karampour Gebchag , Reza Heidari , Seyyed Meysam Abtahi-Froushani , Farah Farokhi , Volume 21, Issue 2 (7-2019)
Abstract
Background and Objective: Diabetic mellitus nephropathy is one of the most important implication factors in kidney´s physiological function in diabetes mellitus. Having major role in filtration, in hyperglycemic condition kidney has shown more damages in comparison with other tissues. This study was done to determine the effect of combined Atorvastatin and Zinc oxide on the biochemical and histopathological alterations in kidney of diabetic rats.
Methods: In this experimental study, 40 female Wistar rats were randomly allocated into five groups including normal control (NC), diabetic control (DC), diabetic rats treated with atorvastatin (20mg/kg/bw daily, orally) (D+A), Zinc oxide (30mg/kg/bw daily, orally) (D+Z) and combination of each drug in half dose (daily, orally) (D+A+Z). Diabetes induced in rats by a single intraperitoneal injection of 60mg/kg/bw streptozotocin-diabetic.Animals treated for one month. At the end of the study, kidney weight and body weight and biochemical factors including creatinine and urea were measured to assess renal function. For determing the histopathology of kidney tissue, sections with 4-5 micrometer were stained with hematoxylin and eosin.
Results: The level of serum creatinine and urea was significantly increased in diabetic rats in compare to controls (P<0.05). Treatment of diabetic rats with half doses of combination of atorvastatin and Zinc oxide reduced the level of creatinine, urea and renal tissue damage in comparision with diabetic rats without treatment (P<0.05).
Conclusion: This study showed that the combination of atorvastatin and Zinc oxide has effect on controlling diabetic nephropathy.
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