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Abbreviations: DETAPAC, diethylenetriaminopentaacetic
acid; CDNB, 1-chloro-2,4-dinitrobenzene; EDTA,
ethylenediaminetertaacetic acid; DTNB, 5,5-dithiobis(2-nitrobenzoic
acid); NBT, nitrobluetetrazolium; PMS, phenazine methosulphate;
TBA, 2-thiobarbituric acid; SDS, sodium dodecyl sulphate; NADH,
nicotinamide adenine dinucleotide; NADPH, nicotinamide adenine
dinucleotide phosphate; TNB, 5-thio-(2-nitrobenzoic acid)]
Introduction
The plants and various microbes synthesize various secondary
metabolites having complex chemical structure. Many of these
secondary metabolites have formed the basis of numerous
pharmacological agents.
1,2
The screening of plants has provided an
avenue for new drug discovery and many of the modern drugs have
been isolated from the natural products.
3–5
The modern chemotherapy
drugs have been very useful in cancer treatment however, their
constant use leads to acquired drug resistance.
6,7
The complementary
and alternative medicinal systems as treatment modalities is very
old and they have been followed in various countries.
8
The cancer
patients also use these systems for healthcare in different countries,
which emphasizes the importance of these system.
9–13
This has given
an impetus to screen natural products for new drug discovery.
Helicia nilagirica Bedd. or Pasaltakaza in Mizo language (Family:
Proteaceae) grows in lowlands to montane rain forests, up to an
altitude of 1000 to 2,000 meters. It is also found along the streams,
hilltops and ridges.
14
H. nilagirica is traditionally used by tribals of
Mizoram, India to treat indigestion, stomach ailments, peptic ulcers,
gynaecological disorders, mouth ulcers and urinary tract infections.
H. nilagirica is also used in the treatment of scabies and some skin
disorders.
15,16
H. nilagirica fruits are used in Sikkim to provide
relief to cure cough and cold.
15,16
There has been a recent report
regarding the anti-inflammatory activity of H. nilagirica.
17
The H.
nilagirca aqueous extract has been reported to exert antineoplastic
activity in vitro and in Dalton’s lymphoma ascites cells in tumorized
mice.
15,16
However, the systematic scientific evaluation of antioxidant
enzymes and lipid peroxidation of H. nilagirica has not been studied.
Therefore, the present study was performed to obtain an insight into
the biochemical profile of Dalton’s lymphoma ascites tumour in Swiss
albino mice treated with aqueous extract of Helicia nilagirica.
Materials and methods
Chemicals
Glutathione (reduced), diethylenetriaminopentaacetic
acid (DETAPAC), 1-chloro-2,4-dinitrobenzene (CDNB),
ethylenediaminetertaacetic acid (EDTA), 5,5-dithiobis(2-
nitrobenzoic acid) (DTNB), nitrobluetetrazolium (NBT), phenazine
methosulphate (PMS), sodium azide, 2-thiobarbituric acid (TBA),
sodium dodecyl sulphate (SDS), nicotinamide adenine dinucleotide
(NADH), nicotinamide adenine dinucleotide phosphate (NADPH),
MOJ Anat & Physiol. 2019;6(4):135‒143. 135
©2019 Jagetia et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and build upon your work non-commercially.
Alteration in the activities of antioxidant enzymes
and lipid peroxidation in mice transplanted with
Dalton’s lymphoma ascites tumor by Helicia nilagirica
Bedd
Volume 6 Issue 4 - 2019
Ganesh Chandra Jagetia, Jennifer Zoremsiami
Department of Zoology, Mizoram University, India
Correspondence: Ganesh Chandra Jagetia, 10, Maharana Pratap
Colony, Sector-13, Hiran Magri, Udaipur-313002, India,
Email
Received: May 24, 2019 | Published: August 22, 2019
Abstract
The present study was performed to obtain an insight into the biochemical profile of
Dalton’s lymphoma ascites tumour bearing Swiss albino mice treated with aqueous extract
of Helicia nilagirica. The mice bearing Dalton’s lymphoma ascites tumor was injected
with 175mg/kg body weight of aqueous extract of H. nilagirica for nine consecutive days.
Thereafter, the tumour cells were aspirated at 2, 4, 6, 8, 12 and 24h post drug treatment for
the estimation of glutathione, glutathione-s-transferase, catalase, superoxide dismutase, and
lipid peroxidation. The administration of tumorized mice with H. nilagirica aqueous extract
caused a significant depletion in the glutathione contents and activities of glutathione-s-
transferase, catalase, superoxide dismutase in a time dependent manner up to 24 h post assay
time, when compared to sterile physiological saline treated group. In contrast, treatment of
tumorized mice with H. nilagirica aqueous extract resulted in a time dependent rise in
the lipid peroxidation when compared to sterile physiological saline treated group. Our
study demonstrates that the cytotoxic effect of H. nilagirica aqueous extract on Dalton’s
lymphoma ascites tumour cells may be due to increased lipid peroxidation and reduction
in the glutathione contents, activities of glutathione-s-transferase, catalase, and superoxide
dismutase.
Keywords: mice, Helicia nilagirica, dalton’s lymphoma, glutathione, antioxidant
enzymes, lipid peroxidation
MOJ Anatomy & Physiology
Research Article
Open Access