Bioactive Compounds Effective Against Type 2 Diabetes Mellitus: A Systematic Review.

(T2DM) Anti-diabetic agents Bioactive compounds Flavonoids. Medicinal plants Phytochemicals Polyphenols Type 2 diabetes

Journal

Current topics in medicinal chemistry
ISSN: 1873-4294
Titre abrégé: Curr Top Med Chem
Pays: United Arab Emirates
ID NLM: 101119673

Informations de publication

Date de publication:
2021
Historique:
received: 20 12 2020
revised: 06 02 2021
accepted: 08 03 2021
pubmed: 11 5 2021
medline: 16 11 2021
entrez: 10 5 2021
Statut: ppublish

Résumé

Type 2 diabetes (adult onset diabetes) is the most common type of diabetes, accounting for around 90% of all diabetes cases with insulin resistance and insulin secretion defect. The key goal of anti-diabetic therapy is to increase the development of insulin, immunity and/or decrease the amount of blood glucose. While many synthetic compounds have been produced as antidiabetic agents, due to their side effects and limited effectiveness, their usefulness has been hindered. This systematic review investigated the bioactive compounds reported to possess activities against type 2 diabetes. Three (3) databases, PubMed, ScienceDirect and Google Scholar were searched for research articles published between January 2010 and October 2020. A total of 6464 articles were identified out of which 84 articles were identified to be elligible for the study. From the data extracted, it was found that quercetin, Kaempferol, Rosmarinic acid, Cyanidin, Rutin, Catechin, Luteolin and Ellagic acid were the most cited bioactive compounds which all falls within the class of polyphenolic compounds. The major sources of these bioactive compounds includes citrus fruits, grapes, onions, berries, cherries, broccoli, honey, apples, green tea, Ginkgo biloba, St. John's wort, green beans, cucumber, spinach, tea, Rosmarinus officinalis, Aloe vera, Moringa oleifera, tomatoes, potatoes, oregano, lemon balm, thyme, peppermint, Ocimum basilicum, red cabbage, pears, olive oil and walnut.

Sections du résumé

BACKGROUND BACKGROUND
Type 2 diabetes (adult onset diabetes) is the most common type of diabetes, accounting for around 90% of all diabetes cases with insulin resistance and insulin secretion defect. The key goal of anti-diabetic therapy is to increase the development of insulin, immunity and/or decrease the amount of blood glucose. While many synthetic compounds have been produced as antidiabetic agents, due to their side effects and limited effectiveness, their usefulness has been hindered.
METHODS METHODS
This systematic review investigated the bioactive compounds reported to possess activities against type 2 diabetes. Three (3) databases, PubMed, ScienceDirect and Google Scholar were searched for research articles published between January 2010 and October 2020. A total of 6464 articles were identified out of which 84 articles were identified to be elligible for the study.
RESULT AND DISCUSSION CONCLUSIONS
From the data extracted, it was found that quercetin, Kaempferol, Rosmarinic acid, Cyanidin, Rutin, Catechin, Luteolin and Ellagic acid were the most cited bioactive compounds which all falls within the class of polyphenolic compounds. The major sources of these bioactive compounds includes citrus fruits, grapes, onions, berries, cherries, broccoli, honey, apples, green tea, Ginkgo biloba, St. John's wort, green beans, cucumber, spinach, tea, Rosmarinus officinalis, Aloe vera, Moringa oleifera, tomatoes, potatoes, oregano, lemon balm, thyme, peppermint, Ocimum basilicum, red cabbage, pears, olive oil and walnut.

Identifiants

pubmed: 33966619
pii: CTMC-EPUB-115601
doi: 10.2174/1568026621666210509161059
doi:

Substances chimiques

Hypoglycemic Agents 0
Plant Extracts 0

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1067-1095

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Chukwuebuka Egbuna (C)

World Bank Africa Centre of Excellence in Public Health and Toxicological Research (PUTOR), University of Port-Harcourt, Rivers State, Nigeria.

Chinaza G Awuchi (CG)

School of Natural and Applied Sciences, Kampala International University, Kampala, Uganda.

Garima Kushwaha (G)

Department of Biotechnology, Indian Institute of Technology, Roorkee-247667, India.

Mithun Rudrapal (M)

Sandip Institute of Pharmaceutical Sciences, Sandip Foundation, Nashik Maharashtra, India.

Kingsley C Patrick-Iwuanyanwu (KC)

World Bank Africa Centre of Excellence in Public Health and Toxicological Research (PUTOR), University of Port-Harcourt, Rivers State, Nigeria.

Omkar Singh (O)

Department of Chemical Engineering, Indian Institute of Technology Madras, Chennai-600036, India.

Uchenna E Odoh (UE)

Department of Pharmacognosy and Environmental Medicines, Faculty of Pharmaceutical Sciences, University of Nigeria, Nsukka, Nigeria.

Johra Khan (J)

Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Majmaah, 11952, Saudi Arabia.

Jaison Jeevanandam (J)

CQM - Centro de Química da Madeira, Universidade da Madeira, Campus da Penteada, 9020-105 Funchal, Portugal.

Suresh Kumarasamy (S)

PG and Research Centre in Biotechnology, MGR College, Hosur, Krishnagiri -635 130, Tamil Nadu, India.

Vincent O Chukwube (VO)

Department of Pharmacognosy and Environmental Medicines, Faculty of Pharmaceutical Sciences, University of Nigeria, Nsukka, Nigeria.

Mathiyazhagan Narayanan (M)

PG and Research Centre in Biotechnology, MGR College, Hosur, Krishnagiri -635 130, Tamil Nadu, India.

Santwana Palai (S)

Department of Veterinary Pharmacology & Toxicology, College of Veterinary Science and Animal Husbandry, OUAT, Bhubaneswar-751003, Odisha, India.

Mihnea-Alexandru Găman (MA)

Faculty of Medicine, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania & Department of Hematology, Center of Hematology and Bone Marrow Transplantation, Fundeni Clinical Institute, Bucharest, Romania.

Chukwuemelie Z Uche (CZ)

Department of Medical Biochemistry and Molecular Biology, Faculty of Basic Medical Sciences, University of Nigeria, Enugu Campus, Nigeria.

Daprim S Ogaji (DS)

Department of Preventive and Social Medicine, University of Port Harcourt, Rivers State, Nigeria.

Nebechi J Ezeofor (NJ)

Department of Food Technology, School of Applied Science and Technology, Federal Polytechnic, Oko, Anambra State, Nigeria.

Andrew G Mtewa (AG)

Chemistry Section, Malawi Institute of Technology, Malawi University of Science and Technology, P.O. Box 5196, Limbe, Malawi.

Chinyere C Patrick-Iwuanyanwu (CC)

Department of Internal Medicine, Endocrinology, Diabetes and Metabolism Unit, University of Port Harcourt Teaching Hospital, Rivers State, Nigeria.

Shyam S Kesh (SS)

Department of Veterinary Clinical Complex, Faculty of Veterinary and Animal Sciences, West Bengal University of Animal and Fishery Sciences, Kolkata-700037, West Bengal, India.

Chandan Shivamallu (C)

Department of Biotechnology and Bioinformatics, School of Life Sciences, JSS Academy of Higher Education & Research, Mysuru, Karnataka-570 015, India.

Kaliyaperumal Saravanan (K)

PG and Research Department of Zoology, Nehru Memorial College (Autonomous), Puthanampatti - 621 007 Affiliated to Bharathidasan University, Tiruchirappalli, Tamil Nadu, India.

Habibu Tijjani (H)

Department of Biochemistry, Natural Product Research Laboratory, Bauchi State University, Gadau, Nigeria.

Muhammad Akram (M)

Department of Eastern Medicines, Government College University, Faisalabad, Pakistan.

Jonathan C Ifemeje (JC)

Department of Biochemistry, Faculty of Natural Sciences, Chukwuemeka Odumegwu Ojukwu University, Uli Campus, Anambra State -431124, Nigeria.

Michael C Olisah (MC)

Department of Medical Biochemistry, Faculty of Basic Medicine, Chukwuemeka Odumegwu Ojukwu University, Anambra State -431124, Nigeria.

Chukwudi J Chikwendu (CJ)

Department of Biochemistry, Faculty of Natural Sciences, Chukwuemeka Odumegwu Ojukwu University, Uli Campus, Anambra State -431124, Nigeria.

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