Cardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure

Despite several reports on the endocrine-disrupting ability of atrazine in amphibian models, few studies have investigated atrazine toxicity in the heart and cerebellum. This study investigated the effect of atrazine on the unique Ca<sup>2+</sup> channel-dependent receptor (Inositol 1,4,...

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Autores principales: Jaclyn Asouzu Johnson, Pilani Nkomozepi, Prosper Opute, Ejikeme Felix Mbajiorgu
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Lenguaje:EN
Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:c51bb3a8b5e546d98a219627e6410a6c2021-11-11T15:05:27ZCardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure10.3390/app1121100062076-3417https://doaj.org/article/c51bb3a8b5e546d98a219627e6410a6c2021-10-01T00:00:00Zhttps://www.mdpi.com/2076-3417/11/21/10006https://doaj.org/toc/2076-3417Despite several reports on the endocrine-disrupting ability of atrazine in amphibian models, few studies have investigated atrazine toxicity in the heart and cerebellum. This study investigated the effect of atrazine on the unique Ca<sup>2+</sup> channel-dependent receptor (Inositol 1,4,5-trisphosphate; IP<sub>3</sub>R) in the heart and the cerebellum of adult male <i>Xenopus laevis</i> and documented the associated histomorphology changes implicated in cardiac and cerebellar function. Sixty adult male African clawed frogs (<i>Xenopus laevis</i>) were exposed to atrazine (0 µg/L (control), 0.01 µg/L, 200 µg/L, and 500 µg/L) for 90 days. Thereafter, heart and cerebellar sections were processed with routine histological stains (heart) or Cresyl violet (brain), and IP<sub>3</sub>R histochemical localization was carried out on both organs. The histomorphology measurements revealed a significant decrease in the mean percentage area fraction of atrial (0.01 µg/L and 200 µg/L) and ventricular myocytes (200 µg/L) with an increased area fraction of interstitial space, while a significant decrease in Purkinje cells was observed in all atrazine groups <i>(p</i> < 0.008, 0.001, and 0.0001). Cardiac IP<sub>3</sub>R was successfully localized, and its mean expression was significantly increased (atrium) or decreased (cerebellum) in all atrazine-exposed groups, suggesting that atrazine may adversely impair cerebellar plasticity and optimal functioning of the heart due to possible disturbances of calcium release, and may also induce several associated cardiac and neural pathophysiologies in all atrazine concentrations, especially at 500 µg/L.Jaclyn Asouzu JohnsonPilani NkomozepiProsper OputeEjikeme Felix MbajiorguMDPI AGarticleatrazinePurkinjecerebellummyocytestoxicologyIP<sub>3</sub>RsTechnologyTEngineering (General). Civil engineering (General)TA1-2040Biology (General)QH301-705.5PhysicsQC1-999ChemistryQD1-999ENApplied Sciences, Vol 11, Iss 10006, p 10006 (2021)
institution DOAJ
collection DOAJ
language EN
topic atrazine
Purkinje
cerebellum
myocytes
toxicology
IP<sub>3</sub>Rs
Technology
T
Engineering (General). Civil engineering (General)
TA1-2040
Biology (General)
QH301-705.5
Physics
QC1-999
Chemistry
QD1-999
spellingShingle atrazine
Purkinje
cerebellum
myocytes
toxicology
IP<sub>3</sub>Rs
Technology
T
Engineering (General). Civil engineering (General)
TA1-2040
Biology (General)
QH301-705.5
Physics
QC1-999
Chemistry
QD1-999
Jaclyn Asouzu Johnson
Pilani Nkomozepi
Prosper Opute
Ejikeme Felix Mbajiorgu
Cardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure
description Despite several reports on the endocrine-disrupting ability of atrazine in amphibian models, few studies have investigated atrazine toxicity in the heart and cerebellum. This study investigated the effect of atrazine on the unique Ca<sup>2+</sup> channel-dependent receptor (Inositol 1,4,5-trisphosphate; IP<sub>3</sub>R) in the heart and the cerebellum of adult male <i>Xenopus laevis</i> and documented the associated histomorphology changes implicated in cardiac and cerebellar function. Sixty adult male African clawed frogs (<i>Xenopus laevis</i>) were exposed to atrazine (0 µg/L (control), 0.01 µg/L, 200 µg/L, and 500 µg/L) for 90 days. Thereafter, heart and cerebellar sections were processed with routine histological stains (heart) or Cresyl violet (brain), and IP<sub>3</sub>R histochemical localization was carried out on both organs. The histomorphology measurements revealed a significant decrease in the mean percentage area fraction of atrial (0.01 µg/L and 200 µg/L) and ventricular myocytes (200 µg/L) with an increased area fraction of interstitial space, while a significant decrease in Purkinje cells was observed in all atrazine groups <i>(p</i> < 0.008, 0.001, and 0.0001). Cardiac IP<sub>3</sub>R was successfully localized, and its mean expression was significantly increased (atrium) or decreased (cerebellum) in all atrazine-exposed groups, suggesting that atrazine may adversely impair cerebellar plasticity and optimal functioning of the heart due to possible disturbances of calcium release, and may also induce several associated cardiac and neural pathophysiologies in all atrazine concentrations, especially at 500 µg/L.
format article
author Jaclyn Asouzu Johnson
Pilani Nkomozepi
Prosper Opute
Ejikeme Felix Mbajiorgu
author_facet Jaclyn Asouzu Johnson
Pilani Nkomozepi
Prosper Opute
Ejikeme Felix Mbajiorgu
author_sort Jaclyn Asouzu Johnson
title Cardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure
title_short Cardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure
title_full Cardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure
title_fullStr Cardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure
title_full_unstemmed Cardiac and Cerebellar Histomorphology and Inositol 1,4,5-Trisphosphate (IP<sub>3</sub>R) Perturbations in Adult <i>Xenopus laevis</i> Following Atrazine Exposure
title_sort cardiac and cerebellar histomorphology and inositol 1,4,5-trisphosphate (ip<sub>3</sub>r) perturbations in adult <i>xenopus laevis</i> following atrazine exposure
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/c51bb3a8b5e546d98a219627e6410a6c
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