Neuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats

Ching-Yi Tsai,1 Chi Fang,1 Jacqueline CC Wu,1 Chiung-Ju Wu,1 Kuang-Yu Dai,1 Shu-Mi Chen2,3 1Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; 2Pharmacology and Toxicology, School of Medicine, Tzu Chi University, Hualien, Taiwan; 3Departme...

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Autores principales: Tsai CY, Fang C, Wu JCC, Wu CJ, Dai KY, Chen SM
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Publicado: Dove Medical Press 2021
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spelling oai:doaj.org-article:ffb7079a34e8427ca87ac4bd3e93efe52021-12-02T16:26:43ZNeuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats1178-7031https://doaj.org/article/ffb7079a34e8427ca87ac4bd3e93efe52021-08-01T00:00:00Zhttps://www.dovepress.com/neuroinflammation-and-microglial-activation-at-rostral-ventrolateral-m-peer-reviewed-fulltext-article-JIRhttps://doaj.org/toc/1178-7031Ching-Yi Tsai,1 Chi Fang,1 Jacqueline CC Wu,1 Chiung-Ju Wu,1 Kuang-Yu Dai,1 Shu-Mi Chen2,3 1Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; 2Pharmacology and Toxicology, School of Medicine, Tzu Chi University, Hualien, Taiwan; 3Department of Pharmacy, Lotung Poh-Ai Hospital, Yilan, TaiwanCorrespondence: Ching-Yi TsaiInstitute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, 123 Dapi Rd, Kaohsiung 83301, TaiwanTel +886-7-7317123 ext.8598Email cytsai@cgmh.org.twPurpose: Cadmium is a heavy metal and environmental toxicant known to act on the central cardiovascular regulatory mechanisms, and one of its brain targets is the rostral ventrolateral medulla (RVLM), a brainstem site that maintains blood pressure and sympathetic vasomotor tone. The present study assessed the hypothesis that cadmium elicits cardiovascular dysregulation by inducing neuroinflammation and microglial activation, two potential cellular mechanisms, in RVLM.Methods: Adult male Sprague–Dawley rats were used for measuring cardiovascular responses after intravenous administration of cadmium. We further conducted real-time PCR, immunofluorescence staining, in situ determination of mitochondrial superoxide, hematoxylin and eosin staining, and enzyme-linked immunosorbent assay (ELISA) to identify cytokine and chemokine mRNA expression, microglia activation, superoxide production, and necrotic and apoptotic cell death in RVLM.Results: We found animals maintained under propofol anesthesia, intravenous administration of cadmium acetate (4 mg/kg) resulted in an increase, followed by a rebound and a secondary decrease in spontaneous baroreflex-mediated sympathetic vasomotor tone, a progressive reduction in mean arterial pressure and heart rate, alongside augmentation of pro-inflammatory cytokine and chemokine in RVLM. All those cardiovascular and neuroinflammatory events were reversed by pretreatment with an anti-inflammatory drug, pentoxifylline (50 mg/kg, i.p.). There were also concurrent microglial activation, reactive oxygen species production, hypoxia, reduced blood flow, and necrotic and apoptotic cell death in RVLM.Conclusion: Based on these biochemical, pharmacological and morphological observations, we conclude that neuroinflammation and microglial activation at RVLM, and their downstream cellular mechanisms, causally underpin cadmium-induced cardiovascular dysregulation.Keywords: reactive microglia, pro-inflammatory cytokine, RVLM, cardiovascular regulation, ROSTsai CYFang CWu JCCWu CJDai KYChen SMDove Medical Pressarticlereactive microgliapro-inflammatory cytokinervlmcardiovascular regulationrosPathologyRB1-214Therapeutics. PharmacologyRM1-950ENJournal of Inflammation Research, Vol Volume 14, Pp 3863-3877 (2021)
institution DOAJ
collection DOAJ
language EN
topic reactive microglia
pro-inflammatory cytokine
rvlm
cardiovascular regulation
ros
Pathology
RB1-214
Therapeutics. Pharmacology
RM1-950
spellingShingle reactive microglia
pro-inflammatory cytokine
rvlm
cardiovascular regulation
ros
Pathology
RB1-214
Therapeutics. Pharmacology
RM1-950
Tsai CY
Fang C
Wu JCC
Wu CJ
Dai KY
Chen SM
Neuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats
description Ching-Yi Tsai,1 Chi Fang,1 Jacqueline CC Wu,1 Chiung-Ju Wu,1 Kuang-Yu Dai,1 Shu-Mi Chen2,3 1Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; 2Pharmacology and Toxicology, School of Medicine, Tzu Chi University, Hualien, Taiwan; 3Department of Pharmacy, Lotung Poh-Ai Hospital, Yilan, TaiwanCorrespondence: Ching-Yi TsaiInstitute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, 123 Dapi Rd, Kaohsiung 83301, TaiwanTel +886-7-7317123 ext.8598Email cytsai@cgmh.org.twPurpose: Cadmium is a heavy metal and environmental toxicant known to act on the central cardiovascular regulatory mechanisms, and one of its brain targets is the rostral ventrolateral medulla (RVLM), a brainstem site that maintains blood pressure and sympathetic vasomotor tone. The present study assessed the hypothesis that cadmium elicits cardiovascular dysregulation by inducing neuroinflammation and microglial activation, two potential cellular mechanisms, in RVLM.Methods: Adult male Sprague–Dawley rats were used for measuring cardiovascular responses after intravenous administration of cadmium. We further conducted real-time PCR, immunofluorescence staining, in situ determination of mitochondrial superoxide, hematoxylin and eosin staining, and enzyme-linked immunosorbent assay (ELISA) to identify cytokine and chemokine mRNA expression, microglia activation, superoxide production, and necrotic and apoptotic cell death in RVLM.Results: We found animals maintained under propofol anesthesia, intravenous administration of cadmium acetate (4 mg/kg) resulted in an increase, followed by a rebound and a secondary decrease in spontaneous baroreflex-mediated sympathetic vasomotor tone, a progressive reduction in mean arterial pressure and heart rate, alongside augmentation of pro-inflammatory cytokine and chemokine in RVLM. All those cardiovascular and neuroinflammatory events were reversed by pretreatment with an anti-inflammatory drug, pentoxifylline (50 mg/kg, i.p.). There were also concurrent microglial activation, reactive oxygen species production, hypoxia, reduced blood flow, and necrotic and apoptotic cell death in RVLM.Conclusion: Based on these biochemical, pharmacological and morphological observations, we conclude that neuroinflammation and microglial activation at RVLM, and their downstream cellular mechanisms, causally underpin cadmium-induced cardiovascular dysregulation.Keywords: reactive microglia, pro-inflammatory cytokine, RVLM, cardiovascular regulation, ROS
format article
author Tsai CY
Fang C
Wu JCC
Wu CJ
Dai KY
Chen SM
author_facet Tsai CY
Fang C
Wu JCC
Wu CJ
Dai KY
Chen SM
author_sort Tsai CY
title Neuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats
title_short Neuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats
title_full Neuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats
title_fullStr Neuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats
title_full_unstemmed Neuroinflammation and Microglial Activation at Rostral Ventrolateral Medulla Underpin Cadmium-Induced Cardiovascular Dysregulation in Rats
title_sort neuroinflammation and microglial activation at rostral ventrolateral medulla underpin cadmium-induced cardiovascular dysregulation in rats
publisher Dove Medical Press
publishDate 2021
url https://doaj.org/article/ffb7079a34e8427ca87ac4bd3e93efe5
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