In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents

Diabetes mellitus is one of the most prevalent diseases in the worldwide population. The impairment in insulin secretion, insulin action or both has led to the hyperglycaemic condition. In 2019, 4.2 million deaths were reported due to diabetes mellitus. Uncontrolled hyperglycaemia condition leads...

Full description

Saved in:
Bibliographic Details
Main Author: Noriman, Ahmad Zakwan
Format: Thesis
Language:English
Published: 2021
Subjects:
Online Access:http://eprints.usm.my/58210/1/Ahmad%20Zakwan-24%20pages.pdf
Tags: Add Tag
No Tags, Be the first to tag this record!
id my-usm-ep.58210
record_format uketd_dc
spelling my-usm-ep.582102023-04-26T03:50:39Z In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents 2021 Noriman, Ahmad Zakwan R Medicine Diabetes mellitus is one of the most prevalent diseases in the worldwide population. The impairment in insulin secretion, insulin action or both has led to the hyperglycaemic condition. In 2019, 4.2 million deaths were reported due to diabetes mellitus. Uncontrolled hyperglycaemia condition leads to secondary complications such as retinopathy, nephropathy, cardiomyopathy, and limb amputation. Thus, one of the plants found in Malaysia, known as Endiandra kingiana (Pokok Medang) was evaluated. It has in vitro α-glucosidase inhibitory effect but lacking evidence in in vivo antidiabetic properties. Thus, there is merit to evaluate the antidiabetic effects of oral crude bark E. kingiana ethanolic extract (EKEE) on Type 2 diabetic rats (T2DR). The study was divided into acute phase (24 hours) and subacute phase (28 days). T2DR was induced by a combination of high-fat diet (HFD) and low-dose streptozotocin (STZ) (30 mg/kg). A dose of EKEE at 250 mg/kg was found to be most effective in lowering fasting blood glucose (FBS) in the acute study. The effect was further evaluated over 28 days in a sub-acute study. Thirty male Sprague-Dawley (SD) rats were divided into 4 groups. Group 1 – normal, Group 2 – untreated-diabetic rats, Group 3 – diabetic rats on EKEE (250 mg/kg) and Group 4 – diabetic rats on metformin (300 mg/kg). FBS, body weight, BMI and SBP were monitored biweekly. At the end of the study, renal function test, liver function test, lipid profiles, glucagon, and oxidative stress markers were evaluated. EKEE did not significantly reduce FBS. EKEE also did not prevent the reduction of body weight and BMI. Glucagon remains normal with EKEE. As for oxidative stress markers, EKEE significantly decreased MDA, and increased total antioxidative capacity, but not significant. These results suggested further study are needed to evaluate E. kingiana as an antidiabetic agent. 2021 Thesis http://eprints.usm.my/58210/ http://eprints.usm.my/58210/1/Ahmad%20Zakwan-24%20pages.pdf application/pdf en public masters Universiti Sains Malaysia Pusat Pengajian Sains Perubatan
institution Universiti Sains Malaysia
collection USM Institutional Repository
language English
topic R Medicine
spellingShingle R Medicine
Noriman, Ahmad Zakwan
In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents
description Diabetes mellitus is one of the most prevalent diseases in the worldwide population. The impairment in insulin secretion, insulin action or both has led to the hyperglycaemic condition. In 2019, 4.2 million deaths were reported due to diabetes mellitus. Uncontrolled hyperglycaemia condition leads to secondary complications such as retinopathy, nephropathy, cardiomyopathy, and limb amputation. Thus, one of the plants found in Malaysia, known as Endiandra kingiana (Pokok Medang) was evaluated. It has in vitro α-glucosidase inhibitory effect but lacking evidence in in vivo antidiabetic properties. Thus, there is merit to evaluate the antidiabetic effects of oral crude bark E. kingiana ethanolic extract (EKEE) on Type 2 diabetic rats (T2DR). The study was divided into acute phase (24 hours) and subacute phase (28 days). T2DR was induced by a combination of high-fat diet (HFD) and low-dose streptozotocin (STZ) (30 mg/kg). A dose of EKEE at 250 mg/kg was found to be most effective in lowering fasting blood glucose (FBS) in the acute study. The effect was further evaluated over 28 days in a sub-acute study. Thirty male Sprague-Dawley (SD) rats were divided into 4 groups. Group 1 – normal, Group 2 – untreated-diabetic rats, Group 3 – diabetic rats on EKEE (250 mg/kg) and Group 4 – diabetic rats on metformin (300 mg/kg). FBS, body weight, BMI and SBP were monitored biweekly. At the end of the study, renal function test, liver function test, lipid profiles, glucagon, and oxidative stress markers were evaluated. EKEE did not significantly reduce FBS. EKEE also did not prevent the reduction of body weight and BMI. Glucagon remains normal with EKEE. As for oxidative stress markers, EKEE significantly decreased MDA, and increased total antioxidative capacity, but not significant. These results suggested further study are needed to evaluate E. kingiana as an antidiabetic agent.
format Thesis
qualification_level Master's degree
author Noriman, Ahmad Zakwan
author_facet Noriman, Ahmad Zakwan
author_sort Noriman, Ahmad Zakwan
title In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents
title_short In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents
title_full In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents
title_fullStr In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents
title_full_unstemmed In vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents
title_sort in vivo activities of ethanolic extract from endiandra kingiana (lauraceae) as potential anti-diabetic agents
granting_institution Universiti Sains Malaysia
granting_department Pusat Pengajian Sains Perubatan
publishDate 2021
url http://eprints.usm.my/58210/1/Ahmad%20Zakwan-24%20pages.pdf
_version_ 1776101212703162368