Authors :
Onoja, A. O; Edogbanya, P. R. O; Egbeja, T. I; Olasunkanmi M. O; Shuaib J
Volume/Issue :
Volume 6 - 2021, Issue 4 - April
Google Scholar :
http://bitly.ws/9nMw
Scribd :
https://bit.ly/2RpuekY
Abstract :
Lung cancer, amongst other forms of cancer
is heterogeneous diseases with diverse morphological
appearances as well as chemotherapeutic responses due
to associated significant limitations in safety and
efficacy. The major risk factor for lung cancer is tobacco
which accounts for 25–30% incidence and 71% of global
lung cancer-related deaths. Tobacco contains Polycyclic
Aromatic Hydrocarbons (PAHs) carcinogens such as
benzo(a)pyrene (B(a)P) which can be activated by a P450 enzymes and covalently bind to DNA at specific sites
to form bulky adducts preceding mutation,
carcinogenesis, apoptosis or nucleotide excision repair
system error. Several plant materials have been
considered as effective in cancer chemoprevention with
negligible or no side effects. This current study was
aimed at determining the Chemopreventive potentials of
aqueous extracts of the whole plant of Phyllanthus
amarus and Euphorbia hirta on B(a)P-induced lung cell
proliferation in albino mice based on selected indices
(phytochemical screening, heamatology and
histopathology). P. amarus and E. hirta, Forty (40)
Pathogen free Swiss albino mice weighing 16g-23g and
B(a)P were used for the study. Decoction extraction
method was employed in the preparation of aqueous
extract of P. amarus and E. hirta whole plants.
Quantitative phytochemical screening of aqueous whole
plant extract was employed using standard procedure.
The mice were blindly divided into eight (8) groups
consisting of five mice (n=5) each per group. The first
two groups are controlled groups (positive PC and
negative NC) the PC received 20mg/kg B(a)P once
weekly while other groups received 20mg/kg B(a)P once
weekly and 50mg/kg, 100mg/kg and 200mg/kg extracts
respectively once daily through oral gavaging. Haemoanalyzer was used to analyze blood sample collected by
cardiac puncture into a pre-labeled EDTA sample
bottles for WBC, LYM, NEUT and BAS while
haematoxylin and eosin method were used for
histological assay. The quantitative phytochemical
analysis reveals the presence of some secondary
metabolites, alkaloids, flavonoids, saponins, tannins,
cardiac glycosides and total phenols. Total phenol was
found to be present in the highest concentration (1044.17
± 0.78, 2015.25 ± 0.01, 1859.12 ± 0.01; P. amarus > E.
hirta > P.amarus and E. hirta) while Cardiac glycoside
have the lowest concentration (0.19 ± 0.00, 0.17 ± 0.00,
0.31 ± 0.01; P.amarus and E. hirta > P.amarus > E. hirta).
The haematological parameter reveals a slight increase
in WBC and LYM in the treated groups which indicates
the strengthening of the defense mechanism as well as
immune response of the organism towards B(a)P
induced cell proliferation. The histological sections of
lung tissue revealed the presence of vessels with mild and
focal lesions in the treated animal groups suggesting the
extracts curative and suppressive effects to the
proliferating cell-tissue and damages induced by B(a)P.
This study has shown that the extracts of P. amarus and
E. hirta could be used as a prophylactic against B(a)Pinduced cell proliferation in the lung tissues of mice. It
also identifies new areas of research for development of
better therapeutic and chemopreventive agents against
carcinogenesis and other infectious diseases. Lastly, this
study serves as a resource base for more research on
molecular indices, biochemical screening and isolation of
active compounds to determine the therapeutic and
chemoprevention efficiency of the plants in lung cancer
treatment in human
Keywords :
Lung cancer, B(a)P, Phyllanthus amarus, Euphorbia hirta, chemoprevention, histopathology.
Lung cancer, amongst other forms of cancer
is heterogeneous diseases with diverse morphological
appearances as well as chemotherapeutic responses due
to associated significant limitations in safety and
efficacy. The major risk factor for lung cancer is tobacco
which accounts for 25–30% incidence and 71% of global
lung cancer-related deaths. Tobacco contains Polycyclic
Aromatic Hydrocarbons (PAHs) carcinogens such as
benzo(a)pyrene (B(a)P) which can be activated by a P450 enzymes and covalently bind to DNA at specific sites
to form bulky adducts preceding mutation,
carcinogenesis, apoptosis or nucleotide excision repair
system error. Several plant materials have been
considered as effective in cancer chemoprevention with
negligible or no side effects. This current study was
aimed at determining the Chemopreventive potentials of
aqueous extracts of the whole plant of Phyllanthus
amarus and Euphorbia hirta on B(a)P-induced lung cell
proliferation in albino mice based on selected indices
(phytochemical screening, heamatology and
histopathology). P. amarus and E. hirta, Forty (40)
Pathogen free Swiss albino mice weighing 16g-23g and
B(a)P were used for the study. Decoction extraction
method was employed in the preparation of aqueous
extract of P. amarus and E. hirta whole plants.
Quantitative phytochemical screening of aqueous whole
plant extract was employed using standard procedure.
The mice were blindly divided into eight (8) groups
consisting of five mice (n=5) each per group. The first
two groups are controlled groups (positive PC and
negative NC) the PC received 20mg/kg B(a)P once
weekly while other groups received 20mg/kg B(a)P once
weekly and 50mg/kg, 100mg/kg and 200mg/kg extracts
respectively once daily through oral gavaging. Haemoanalyzer was used to analyze blood sample collected by
cardiac puncture into a pre-labeled EDTA sample
bottles for WBC, LYM, NEUT and BAS while
haematoxylin and eosin method were used for
histological assay. The quantitative phytochemical
analysis reveals the presence of some secondary
metabolites, alkaloids, flavonoids, saponins, tannins,
cardiac glycosides and total phenols. Total phenol was
found to be present in the highest concentration (1044.17
± 0.78, 2015.25 ± 0.01, 1859.12 ± 0.01; P. amarus > E.
hirta > P.amarus and E. hirta) while Cardiac glycoside
have the lowest concentration (0.19 ± 0.00, 0.17 ± 0.00,
0.31 ± 0.01; P.amarus and E. hirta > P.amarus > E. hirta).
The haematological parameter reveals a slight increase
in WBC and LYM in the treated groups which indicates
the strengthening of the defense mechanism as well as
immune response of the organism towards B(a)P
induced cell proliferation. The histological sections of
lung tissue revealed the presence of vessels with mild and
focal lesions in the treated animal groups suggesting the
extracts curative and suppressive effects to the
proliferating cell-tissue and damages induced by B(a)P.
This study has shown that the extracts of P. amarus and
E. hirta could be used as a prophylactic against B(a)Pinduced cell proliferation in the lung tissues of mice. It
also identifies new areas of research for development of
better therapeutic and chemopreventive agents against
carcinogenesis and other infectious diseases. Lastly, this
study serves as a resource base for more research on
molecular indices, biochemical screening and isolation of
active compounds to determine the therapeutic and
chemoprevention efficiency of the plants in lung cancer
treatment in human
Keywords :
Lung cancer, B(a)P, Phyllanthus amarus, Euphorbia hirta, chemoprevention, histopathology.