Evaluation of Anti Hyperlipidemic Effect of Zinc Sulfate Alone and in Combination with Atorvastatin in Diet Induced Hyperlipidemic Rats

Background: Hyperlipidemia a lipid disorder that affects millions of people worldwide. It is a major contributor for developing cardiovascular diseases. Objective: To assess the antihyperlipidemic activity of zinc sulfate alone and in combination with atorvastatin in diet induced hyperlipidemic rats. Methods: Randomized clinical trial was conducted for 8 weeks in Post graduate Medical Institute, Lahore. Thirty -six healthy male albino rats weighing between 100-160mg were randomly divided into 6 groups each having 6 rats. Group A normal control (fed with rat chow) and Group B disease control (fed with high fat diet). Groups C,D,E and F, were experimental groups, fed with high fat diet during the initial four weeks to produce hyperlipidemia and during next four weeks, along with high fat diet (30 mg/kg zinc sulfate orally) was added to Group C, (40 mg/kg Atorvastatin orally) to Group D (30 mg/kg of zinc sulfate + 40 mg/kg atorvastatin) to Group E and (15 mg/kg zinc sulfate +20 mg/kg atorvastatin) to Group F. Blood samples were drawn at 0, 4 and 8 weeks and serum was assessed for lipid profile. Rats were sacrificed at the end of 8 weeks and liver samples examined for histopathological examination. Results: Disease control group showed significant rise in total cholesterol from 80.17±17.82 at 0 week to 177.17± 15.96, low density lipoprotein from 32.62±17.15 to 102.03±10.88, and triglycerides from 58.17±23.79 to 159.00±39.83 with a p-value of <0.05. All the experimental groups improved lipid profile compared to disease control group a p-value of <0.001. All experimental groups increased high density lipoprotein compared to disease control group, most significant increase was seen in group E (63.00±5.29) with a p-value of 0.010. Histopathological examination showed, 66.7% of rats in disease control group had severe steatosis. Among the experimental groups, Group D had 33.3 % rats while Group C, E, and F had no animal with severe steatosis. Conclusion: Zinc supplementation alone and in combination with atorvastatin has shown beneficial effects on lipid profile. Zinc sulfate also reduced the fatty alterations of hepatic architecture.

Authors

Institutions

Publication Details

Journal
Annals of King Edward Medical University
Published
2025-09-30
DOI
https://doi.org/10.21649/akemu.v31i3.5622
Primary Topic
Diabetes, Cardiovascular Risks, and Lipoproteins
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Evaluation of Anti Hyperlipidemic Effect of Zinc Sulfate Alone and in Combination with Atorvastatin in Diet Induced Hyperlipidemic Rats

Sadaf Humayun Khan, Samreen Hameed, Raana Akhtar, Hannah Pirzada et al.
Annals of King Edward Medical University
Diabetes, Cardiovascular Risks, and Lipoproteins
article

Evaluation of Anti Hyperlipidemic Effect of Zinc Sulfate Alone and in Combination with Atorvastatin in Diet Induced Hyperlipidemic Rats

Sadaf Humayun Khan, Samreen Hameed, Raana Akhtar, Hannah Pirzada, Humaira Talat, Wardah Siddique
article en

Abstract

Background: Hyperlipidemia a lipid disorder that affects millions of people worldwide. It is a major contributor for developing cardiovascular diseases. Objective: To assess the antihyperlipidemic activity of zinc sulfate alone and in combination with atorvastatin in diet induced hyperlipidemic rats. Methods: Randomized clinical trial was conducted for 8 weeks in Post graduate Medical Institute, Lahore. Thirty -six healthy male albino rats weighing between 100-160mg were randomly divided into 6 groups each having 6 rats. Group A normal control (fed with rat chow) and Group B disease control (fed with high fat diet). Groups C,D,E and F, were experimental groups, fed with high fat diet during the initial four weeks to produce hyperlipidemia and during next four weeks, along with high fat diet (30 mg/kg zinc sulfate orally) was added to Group C, (40 mg/kg Atorvastatin orally) to Group D (30 mg/kg of zinc sulfate + 40 mg/kg atorvastatin) to Group E and (15 mg/kg zinc sulfate +20 mg/kg atorvastatin) to Group F. Blood samples were drawn at 0, 4 and 8 weeks and serum was assessed for lipid profile. Rats were sacrificed at the end of 8 weeks and liver samples examined for histopathological examination. Results: Disease control group showed significant rise in total cholesterol from 80.17±17.82 at 0 week to 177.17± 15.96, low density lipoprotein from 32.62±17.15 to 102.03±10.88, and triglycerides from 58.17±23.79 to 159.00±39.83 with a p-value of <0.05. All the experimental groups improved lipid profile compared to disease control group a p-value of <0.001. All experimental groups increased high density lipoprotein compared to disease control group, most significant increase was seen in group E (63.00±5.29) with a p-value of 0.010. Histopathological examination showed, 66.7% of rats in disease control group had severe steatosis. Among the experimental groups, Group D had 33.3 % rats while Group C, E, and F had no animal with severe steatosis. Conclusion: Zinc supplementation alone and in combination with atorvastatin has shown beneficial effects on lipid profile. Zinc sulfate also reduced the fatty alterations of hepatic architecture.

Annals of King Edward Medical UniversityVol. 31(3)
King Edward Medical University (PK), University of Lahore (PK), Rawalpindi Medical University (PK), Fatima Jinnah Medical University (PK), Nishtar Medical College and Hospital (PK), Allama Iqbal Medical College (PK), University College Lahore (PK)
Openalex Percentile: Top 54%
Diabetes, Cardiovascular Risks, and Lipoproteins
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.