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Authors
Info
G.K. Pitchika1,2, K.V.
Swamy3,
T.S. Ranjani1, C.R.
Tyler4,
S.B. Sainath5 and G.H.
Phillip1*
1Department of
Zoology, Sri
Krishnadevaraya University,
Anantapur-515 003,
India
2Department of
Zoology, Vikrama
Simhapuri University PG Centre,
Kavali-524 201,
India
3Department of
Bioinformatics
and Computer Science,
Dr. D.Y. Patil Biotechnology
and Bioinformatics Institute,
Pune-411 033,
India
4Biosciences,
College of Life and
Environmental Sciences, University
of Exeter, Exeter,
EX4 4QD, UK
5Department of
Biotechnology,
Vikrama Simhapuri University,
Nellore-524 320, India
*Corresponding
Author Email :
pitchika.gopikrishna@gmail.com
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Abstract
Aim: The aim of the
present study was to evaluate the reproductive efficacy of male and female
zebrafish following cypermethrin exposure.
Methodology: The adult
zebrafish (Danio rerio) of both sexes were exposed to cypermethrin at
three selected concentrations 0.1, 1.0 and 10 ?gl-1 over a period
of 21days. After completion of experimental period, the reproductive
endpoints such as fecundity, hatchability, testis and ovarian histology and
plasma vitellogenin levels were selected and determined in this study.
Results: Cypermethrin
exposure did not affect the cumulative fecundity rates in experimental fishes
over controls. However, cypermethrin at 10 ?gl-1 showed a
significant reduction in the sperm number in male fishes over control. On the
other hand, the same concentration of cypermethrin did not show significant
changes in the plasma vitellogenin levels of both male and female fishes over
their respective controls. Analysis of testicular and ovarian architectures
of male and female zebrafish exposed to cypermethrin at 10 ?gl-1
showed no marked differences over controls. In addition, molecular docking
studies revealed that the binding energy between the cypermethrin and
zebrafish estrogen receptor (zfER) β1 was almost similar to the binding
energies exhibited by reference molecules, estradiol and ethinyl estradiol
with zfERβ1. Further, binding energies between the ligands (cypermethrin
and its metabolites phenoxybenzaldehyde and 3-phenoxybenzoic acid) with
zfERα were low as compared to the binding energies between the reference
molecules and zfERα.
Interpretation: In-vivo
studies indicated that cypermethrin at 10?g l-1 leads to
spermatotoxicity in zebrafish and in silico analysis showed that the
cypermethrin at least in part interfere with the signalling of zfERα.
Key words: Cypermethrin, Estrogen receptors, Spermatogenesis,
Zebrafish
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