Bioactive Carbohydrates and Dietary Fibre 24 (2020) 100237
Available online 30 August 2020
2212-6198/© 2020 Elsevier Ltd. All rights reserved.
Evaluation of the pancreatoprotective effect of algal extracts on
Alloxan-induced diabetic rat
Eman A. Alwaleed
a, *
, Asmaa Jillany
a
, Naglaa R.A. Kasem
b
, Hamdy Galal
a
a
Department of Botany, Faculty of Science, South Valley University, Qena, Egypt
b
Department of Zoology, Faculty of Science, South Valley University, Qena, Egypt
A R T I C L E INFO
Keywords:
Halimeda opuntia
Polycladia myrica
Diabetes
Kidney function
ABSTRACT
Purpose: Diabetes is a metabolic syndrome which is associated with the worldwide major public health problems.
In the present research, with respect to the traditional and ethnic uses of Polycladia myrica and Halimeda opuntia
algal extract for healing of diabetic diseases.
Materials and methods: algal extracts at 100 and 200 mg/kg was administered orally to Alloxan-induced diabetic
rats once daily for 15 days. Serum glucose levels, Complete Blood Count (CBC) and Kidney function of rats were
measured at the end of experimental. The liver function of the pancreas was also observed.
Results: The preprandial and postprandial glucose levels in the group treated with algal extracts (100 and 200
mg/kg) were signifcantly reduced compared with those of the diabetes group. Additionally, the levels of CBC,
kidney function and liver function in the 100 and 200 mg/kg algal extract were signifcantly different from those
in the diabetes group.
Conclusion: The results illustrated that, algal extracts at 100 & 200 mg/kg had the best capability to lower the
levels of glucose and we can conclude that Halimeda extract is the best effective extract as preventive medication
(pre-treatment) and the polycladia extract with concentration 100 is the best effective extract as medication
(post-treatment).
1. Introduction
Algae take considerable position among living organisms because of
their features that make them categorized as a potent and hopeful sys-
tem as a natural resource. They are signifcant in various applications as
antimicrobial, anti-viral, anti-oxidants, anticancer, anti-diabetic and
anti-infammatory (Yu, Shen, Song, & Xie, 2018). Marine algae have
essential actions for diabetes prevention and administration due to the
healthy nutritional structure that may support diabetics such as, un-
saturated fatty acids, dietary fbers in addition to bioactive composition
(Sharifuddin, Chin, Lim, & Phang, 2015).
Diabetes mellitus (DM) is one of the great congregations and chronic
defects of carbohydrate, lipid and protein metabolism described by
continue rise of blood glucose levels. This cans either product from a
fractional or complex stopping of insulin excretion or making, or resis-
tance to insulin work (Longe, Momoh, & Adepoju, 2015).
Survey on anti-diabetic potential of marine algae is generally
nonhomogeneous as certain seaweed components, bioactive compounds
and mechanisms of action have been tested relatively more wide than
others. Apart from unsaturated fatty acids and dietary fbers, studies on
anti-diabetic features involving polyphenols from seaweed are consid-
erably more common with a diversity of polyphenolic components iso-
lated versus many well-known anti-diabetic targets. Polyphenolic
components are famous for making complexes upon interaction with
different proteins (Sharifuddin et al., 2015). And those extracted from
vegetables and fruits display several activities comprising anti-diabetes
(Anhˆ e et al., 2013). The anti-diabetic targets of marine algae bioactive
compounds comprising repression of enzymes involved in maintenance
of glucose homeostasis like α-amylase, α-glucosidase, aldose reductase
and protein tyrosine phosphatase 1B (PTP1B), suppression of incretin
hormones activities, stimulating of glucose uptake by cells, anti-obesity,
anti-infammation as well as cytoprotection of β-cells (Sharifuddin et al.,
2015).
* Corresponding author.
E-mail address: Eme_biologist@sci.svu.edu.eg (E.A. Alwaleed).
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Bioactive Carbohydrates and Dietary Fibre
journal homepage: http://www.elsevier.com/locate/bcdf
https://doi.org/10.1016/j.bcdf.2020.100237
Received 6 January 2020; Received in revised form 10 July 2020; Accepted 6 August 2020