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In vitro anti-diabetic activities and phytochemical analysis of bioactive fractions present in Meriandra dianthera, Aloe camperi and a Polyherb

In vitro anti-diabetic activities and phytochemical analysis of bioactive fractions present in Meriandra dianthera, Aloe camperi and a Polyherb
In vitro anti-diabetic activities and phytochemical analysis of bioactive fractions present in Meriandra dianthera, Aloe camperi and a Polyherb
This paper reports the in vitro anti-diabetic profile of certain medicinal plants traditionally used in Eritrea for the management of type 2 diabetes. The crude methanolic extracts and fractions of Meriandra dianthera, Aloe camperi, a Polyherb and their fractions were investigated. The in vitro screening of the crude extracts has generally elicited a dose dependent α-glucosidase and α-amylase inhibition activities. M. dianthera displayed the highest α-glucosidase inhibitory activity (IC50: 0.074 ± 0.032 mg/mL) at the highest concentration tested (0.800 mg/mL) relative to A. camperi, the Polyherb and Acarbose (IC50: 0.37 ± 0.052, 0.56 ± 0.024 and 0.55 ± 0.029 respectively). The α-glucosidase inhibition activities of A. camperi and M. dianthera, except for the Polyherb and Acarbose, were significantly different (P < 0.05) at various ranges of concentrations (0.025 - 0.800 mg/mL). The percentage α-amylase inhibitions of M. dianthera, A. camperi, the Polyherb and Acarbose, at the highest concentrations (0.800 mg/mL), were 78.3%, 15.9%, 16.4%, and 82.9% respectively. A. camperi and the Polyherb displayed lower α-amylase inhibitory activities (IC50: 1.72 ± 0.06 and 2.57 ± 0.07 mg/mL respectively) compared to Acarbose and M. dianthera (IC50: 0.31 ± 0.01 and 0.43 ± 0.02 mg/mL respectively). For the α-amylase inhibition activity, even at lower concentrations (0.025 mg/mL), there were statistically significant differences (P < 0.01) among the values generated for all the extracts. The in vitro anti-diabetic screening of the fractions, at 0.800 mg/ml, displayed characteristic enzyme inhibition activities. Generally, the non-polar fractions showed higher enzyme inhibitory activities compared to the polar fractions. The most bioactive non-polar fractions, thus, were subjected to GC-MS analysis and presented various essential oils, fatty acid methyl esters (FAMEs) and benzoic acid derivatives in those plants.
anti-diabetic, α-Glucosidase, α-Amylase, GC-MS, Essential Oils, Fatty Acid Methyl Esters
2158-2742
533-544
Sium, Mussie
153c2eeb-9370-461b-9a9d-473768245d9c
Kareru, Patrick
4eb9754a-165a-4910-9c4d-939915bc7053
Kiage-Mokua, Beatrice
df9c1e3f-2c19-4d8a-9b85-e5605b9e5e1e
Sood, Kaushal
8d78428b-f4f8-4f6b-862e-547aa65d71b1
Langley, John
7ac80d61-b91d-4261-ad17-255f94ea21ea
Herniman, Julie
530b1a36-1386-4602-8df7-defa6eb3512b
Sium, Mussie
153c2eeb-9370-461b-9a9d-473768245d9c
Kareru, Patrick
4eb9754a-165a-4910-9c4d-939915bc7053
Kiage-Mokua, Beatrice
df9c1e3f-2c19-4d8a-9b85-e5605b9e5e1e
Sood, Kaushal
8d78428b-f4f8-4f6b-862e-547aa65d71b1
Langley, John
7ac80d61-b91d-4261-ad17-255f94ea21ea
Herniman, Julie
530b1a36-1386-4602-8df7-defa6eb3512b

Sium, Mussie, Kareru, Patrick, Kiage-Mokua, Beatrice, Sood, Kaushal, Langley, John and Herniman, Julie (2017) In vitro anti-diabetic activities and phytochemical analysis of bioactive fractions present in Meriandra dianthera, Aloe camperi and a Polyherb. American Journal of Plant Sciences, 2017 (8), 533-544. (doi:10.4236/ajps.2017.83037).

Record type: Article

Abstract

This paper reports the in vitro anti-diabetic profile of certain medicinal plants traditionally used in Eritrea for the management of type 2 diabetes. The crude methanolic extracts and fractions of Meriandra dianthera, Aloe camperi, a Polyherb and their fractions were investigated. The in vitro screening of the crude extracts has generally elicited a dose dependent α-glucosidase and α-amylase inhibition activities. M. dianthera displayed the highest α-glucosidase inhibitory activity (IC50: 0.074 ± 0.032 mg/mL) at the highest concentration tested (0.800 mg/mL) relative to A. camperi, the Polyherb and Acarbose (IC50: 0.37 ± 0.052, 0.56 ± 0.024 and 0.55 ± 0.029 respectively). The α-glucosidase inhibition activities of A. camperi and M. dianthera, except for the Polyherb and Acarbose, were significantly different (P < 0.05) at various ranges of concentrations (0.025 - 0.800 mg/mL). The percentage α-amylase inhibitions of M. dianthera, A. camperi, the Polyherb and Acarbose, at the highest concentrations (0.800 mg/mL), were 78.3%, 15.9%, 16.4%, and 82.9% respectively. A. camperi and the Polyherb displayed lower α-amylase inhibitory activities (IC50: 1.72 ± 0.06 and 2.57 ± 0.07 mg/mL respectively) compared to Acarbose and M. dianthera (IC50: 0.31 ± 0.01 and 0.43 ± 0.02 mg/mL respectively). For the α-amylase inhibition activity, even at lower concentrations (0.025 mg/mL), there were statistically significant differences (P < 0.01) among the values generated for all the extracts. The in vitro anti-diabetic screening of the fractions, at 0.800 mg/ml, displayed characteristic enzyme inhibition activities. Generally, the non-polar fractions showed higher enzyme inhibitory activities compared to the polar fractions. The most bioactive non-polar fractions, thus, were subjected to GC-MS analysis and presented various essential oils, fatty acid methyl esters (FAMEs) and benzoic acid derivatives in those plants.

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Accepted/In Press date: 20 February 2017
Published date: 23 February 2017
Keywords: anti-diabetic, α-Glucosidase, α-Amylase, GC-MS, Essential Oils, Fatty Acid Methyl Esters
Organisations: Characterisation and Analytics, Chemistry Research Support

Identifiers

Local EPrints ID: 407381
URI: http://eprints.soton.ac.uk/id/eprint/407381
ISSN: 2158-2742
PURE UUID: 758c0ba1-d3c9-4603-8ad1-eec6eb950f34
ORCID for John Langley: ORCID iD orcid.org/0000-0002-8323-7235
ORCID for Julie Herniman: ORCID iD orcid.org/0000-0003-4834-1093

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Date deposited: 05 Apr 2017 01:05
Last modified: 16 Mar 2024 03:02

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Contributors

Author: Mussie Sium
Author: Patrick Kareru
Author: Beatrice Kiage-Mokua
Author: Kaushal Sood
Author: John Langley ORCID iD
Author: Julie Herniman ORCID iD

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