Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic diets
Background & objectives: Natural dietary supplements are progressively getting famous to supplant synthetic substances particularly in chronic morbidities. The aim of this study was to evaluate the anti-obesity potential of almond on the normal, Cafeteria, and Atherogenic diets. Materials an...
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2021-07-01
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doaj-1deddc14b68644abbf3a9c65299668302021-06-25T04:46:48ZengElsevierSaudi Journal of Biological Sciences1319-562X2021-07-0128740624068Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic dietsSyed Mohammed Basheeruddin Asdaq0Shrey Tambe1Yahya Mohzari2Ahmed Alrashed3Hamdan Najib Alajami4Awad Othman Aljohani5Abdullah Ali Al Mushtawi6Majed Sultan Alenazy7Rakan Fahad Alamer8Abdulmajead Khalid Alanazi9Syed Imam Rabbani10Department of Pharmacy Practice, College of Pharmacy, AlMaarefa University, Dariyah, 13713 Riyadh, Saudi Arabia; Corresponding author at: Department of Pharmacy Practice, College of Pharmacy, AlMaarefa University, Dariyah, 13713 Riyadh, Saudi Arabia.Department of Pharmacology, Krupanidhi College of Pharmacy, Bangalore 560035, IndiaClinical Pharmacy Department, King Saud Medical City, Riyadh 12746, Saudi ArabiaPharmaceutical Services Administration, Inpatient Department, Main Hospital, KFMC, Riyadh 11564, Saudi ArabiaPharmaceutical Services Administration, King Saud Medical City, Ministry of Health, Riyadh, Saudi ArabiaPharmaceutical Services Administration, King Saud Medical City, Ministry of Health, Riyadh, Saudi ArabiaPharmaceutical Services Administration, King Saud Medical City, Ministry of Health, Riyadh, Saudi ArabiaPharmaceutical Services Administration, King Saud Medical City, Ministry of Health, Riyadh, Saudi ArabiaPharmaceutical Services Administration, King Saud Medical City, Ministry of Health, Riyadh, Saudi ArabiaPharmaceutical Services Administration, King Saud Medical City, Ministry of Health, Riyadh, Saudi ArabiaDepartment of Pharmacology and Toxicology, College of Pharmacy, Qassim University, Buraydah, Saudi ArabiaBackground & objectives: Natural dietary supplements are progressively getting famous to supplant synthetic substances particularly in chronic morbidities. The aim of this study was to evaluate the anti-obesity potential of almond on the normal, Cafeteria, and Atherogenic diets. Materials and methods: Parameters such as change in body weight, body temperature, lipid profile, organ weights, and fat pad weights were assessed. Central Nervous System related studies (Despair Swim test and Elevated Plus maze test) were also performed to comprehend the effect of the diets, and almond on the brain. All of the experimental animals were randomly assigned to one of three diet categoriesregular, cafeteria, or atherogenic, and fed those diets for 40 days. Each diet had the control group, standard drug group and three almond groups (low dose: 50; medium dose: 100 and high dose: 200 mg/kg body weight). Body weight was recorded every alternate day. On 40th day, body temperature was measured. On day 41, lipid parameters, organ weights, fat pad weights and the CNS parameters were evaluated. ANOVA followed by Duncans Multiple Range Test were used for statistical analysis. Results: Treatment of animals with either a low or high dose of almond as well as a standard herb prevented a rise in body weight significantly (p = 0.01) in all three diet groups. When a regular diet was replaced with a cafeteria and atherogenic diet, the serum levels of triglycerides and LDL increased significantly, while HDL levels decreased significantly. Overall, almond preparation reduced lipid parameters, organ weights, fat-pad weights, and stabilized CNS parameters substantially. Interpretation & conclusion: The almond high dose was the most effective of all the almond preparations. Our study suggests that chronic administration of almond independently reduces the body weight in experimental animals.http://www.sciencedirect.com/science/article/pii/S1319562X21002801Lipid parametersObesityCNS parametersAlmondCafeteria dietAtherogenic diet |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Syed Mohammed Basheeruddin Asdaq Shrey Tambe Yahya Mohzari Ahmed Alrashed Hamdan Najib Alajami Awad Othman Aljohani Abdullah Ali Al Mushtawi Majed Sultan Alenazy Rakan Fahad Alamer Abdulmajead Khalid Alanazi Syed Imam Rabbani |
spellingShingle |
Syed Mohammed Basheeruddin Asdaq Shrey Tambe Yahya Mohzari Ahmed Alrashed Hamdan Najib Alajami Awad Othman Aljohani Abdullah Ali Al Mushtawi Majed Sultan Alenazy Rakan Fahad Alamer Abdulmajead Khalid Alanazi Syed Imam Rabbani Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic diets Saudi Journal of Biological Sciences Lipid parameters Obesity CNS parameters Almond Cafeteria diet Atherogenic diet |
author_facet |
Syed Mohammed Basheeruddin Asdaq Shrey Tambe Yahya Mohzari Ahmed Alrashed Hamdan Najib Alajami Awad Othman Aljohani Abdullah Ali Al Mushtawi Majed Sultan Alenazy Rakan Fahad Alamer Abdulmajead Khalid Alanazi Syed Imam Rabbani |
author_sort |
Syed Mohammed Basheeruddin Asdaq |
title |
Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic diets |
title_short |
Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic diets |
title_full |
Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic diets |
title_fullStr |
Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic diets |
title_full_unstemmed |
Anti-obesity potential of almond (Prunus dulcis) in experimental animals under cafeteria and atherogenic diets |
title_sort |
anti-obesity potential of almond (prunus dulcis) in experimental animals under cafeteria and atherogenic diets |
publisher |
Elsevier |
series |
Saudi Journal of Biological Sciences |
issn |
1319-562X |
publishDate |
2021-07-01 |
description |
Background & objectives: Natural dietary supplements are progressively getting famous to supplant synthetic substances particularly in chronic morbidities. The aim of this study was to evaluate the anti-obesity potential of almond on the normal, Cafeteria, and Atherogenic diets. Materials and methods: Parameters such as change in body weight, body temperature, lipid profile, organ weights, and fat pad weights were assessed. Central Nervous System related studies (Despair Swim test and Elevated Plus maze test) were also performed to comprehend the effect of the diets, and almond on the brain. All of the experimental animals were randomly assigned to one of three diet categoriesregular, cafeteria, or atherogenic, and fed those diets for 40 days. Each diet had the control group, standard drug group and three almond groups (low dose: 50; medium dose: 100 and high dose: 200 mg/kg body weight). Body weight was recorded every alternate day. On 40th day, body temperature was measured. On day 41, lipid parameters, organ weights, fat pad weights and the CNS parameters were evaluated. ANOVA followed by Duncans Multiple Range Test were used for statistical analysis. Results: Treatment of animals with either a low or high dose of almond as well as a standard herb prevented a rise in body weight significantly (p = 0.01) in all three diet groups. When a regular diet was replaced with a cafeteria and atherogenic diet, the serum levels of triglycerides and LDL increased significantly, while HDL levels decreased significantly. Overall, almond preparation reduced lipid parameters, organ weights, fat-pad weights, and stabilized CNS parameters substantially. Interpretation & conclusion: The almond high dose was the most effective of all the almond preparations. Our study suggests that chronic administration of almond independently reduces the body weight in experimental animals. |
topic |
Lipid parameters Obesity CNS parameters Almond Cafeteria diet Atherogenic diet |
url |
http://www.sciencedirect.com/science/article/pii/S1319562X21002801 |
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