Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in Rats

This study aims to investigate whether tissue oxidative stress in the rostral ventrolateral medulla (RVLM), where sympathetic premotor neurons reside, plays an active role in age-dependent susceptibility to hypertension in response to nitric oxide (NO) deficiency induced by systemic <span style=&...

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Main Authors: Yung-Mei Chao, Hana Rauchová, Julie Y. H. Chan
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/10/9/2232
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author Yung-Mei Chao
Hana Rauchová
Julie Y. H. Chan
author_facet Yung-Mei Chao
Hana Rauchová
Julie Y. H. Chan
author_sort Yung-Mei Chao
collection DOAJ
description This study aims to investigate whether tissue oxidative stress in the rostral ventrolateral medulla (RVLM), where sympathetic premotor neurons reside, plays an active role in age-dependent susceptibility to hypertension in response to nitric oxide (NO) deficiency induced by systemic <span style="font-variant: small-caps;">l</span>-NAME treatment, and to decipher the underlying molecular mechanisms. Systolic blood pressure (SBP) and heart rate (HR) in conscious rats were recorded, along with measurements of plasma and RVLM level of NO and reactive oxygen species (ROS), and expression of mRNA and protein involved in ROS production and clearance, in both young and adult rats subjected to intraperitoneal (i.p.) infusion of <span style="font-variant: small-caps;">l</span>-NAME. Pharmacological treatments were administered by oral gavage or intracisternal infusion. Gene silencing of target mRNA was made by bilateral microinjection into RVLM of lentivirus that encodes a short hairpin RNA (shRNA) to knock down gene expression of NADPH oxidase activator 1 (<i>Noxa1</i>). We found that i.p. infusion of <span style="font-variant: small-caps;">l</span>-NAME resulted in increases in SBP, sympathetic neurogenic vasomotor activity, and plasma norepinephrine levels in an age-dependent manner. Systemic <span style="font-variant: small-caps;">l</span>-NAME also evoked oxidative stress in RVLM of adult, but not young rats, accompanied by augmented enzyme activity of NADPH oxidase and reduced mitochondrial electron transport enzyme activities. Treatment with L-arginine via oral gavage or infusion into the cistern magna (i.c.), but not i.c. tempol or mitoQ<sub>10</sub>, significantly offset the <span style="font-variant: small-caps;">l</span>-NAME-induced hypertension in young rats. On the other hand, all treatments appreciably reduced <span style="font-variant: small-caps;">l</span>-NAME-induced hypertension in adult rats. The mRNA microarray analysis revealed that four genes involved in ROS production and clearance were differentially expressed in RVLM in an age-related manner. Of them, <i>Noxa1</i>, and <i>GPx2</i> were upregulated and <i>Duox2</i> and <i>Ucp3</i> were downregulated. Systemic <span style="font-variant: small-caps;">l</span>-NAME treatment caused greater upregulation of <i>Noxa1</i>, but not <i>Ucp3</i>, mRNA expression in RVLM of adult rats. Gene silencing of <i>Noxa1</i> in RVLM effectively alleviated oxidative stress and protected adult rats against <span style="font-variant: small-caps;">l</span>-NAME-induced hypertension. These data together suggest that hypertension induced by systemic <span style="font-variant: small-caps;">l</span>-NAME treatment in young rats is mediated primarily by NO deficiency that occurs both in vascular smooth muscle cells and RVLM. On the other hand, enhanced augmentation of oxidative stress in RVLM may contribute to the heightened susceptibility of adult rats to hypertension induced by systemic <span style="font-variant: small-caps;">l</span>-NAME treatment.
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spelling doaj.art-a970c181250c4322819e0310c7bb13b62023-11-23T15:11:22ZengMDPI AGBiomedicines2227-90592022-09-01109223210.3390/biomedicines10092232Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in RatsYung-Mei Chao0Hana Rauchová1Julie Y. H. Chan2Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, TaiwanInstitute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech RepublicInstitute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, TaiwanThis study aims to investigate whether tissue oxidative stress in the rostral ventrolateral medulla (RVLM), where sympathetic premotor neurons reside, plays an active role in age-dependent susceptibility to hypertension in response to nitric oxide (NO) deficiency induced by systemic <span style="font-variant: small-caps;">l</span>-NAME treatment, and to decipher the underlying molecular mechanisms. Systolic blood pressure (SBP) and heart rate (HR) in conscious rats were recorded, along with measurements of plasma and RVLM level of NO and reactive oxygen species (ROS), and expression of mRNA and protein involved in ROS production and clearance, in both young and adult rats subjected to intraperitoneal (i.p.) infusion of <span style="font-variant: small-caps;">l</span>-NAME. Pharmacological treatments were administered by oral gavage or intracisternal infusion. Gene silencing of target mRNA was made by bilateral microinjection into RVLM of lentivirus that encodes a short hairpin RNA (shRNA) to knock down gene expression of NADPH oxidase activator 1 (<i>Noxa1</i>). We found that i.p. infusion of <span style="font-variant: small-caps;">l</span>-NAME resulted in increases in SBP, sympathetic neurogenic vasomotor activity, and plasma norepinephrine levels in an age-dependent manner. Systemic <span style="font-variant: small-caps;">l</span>-NAME also evoked oxidative stress in RVLM of adult, but not young rats, accompanied by augmented enzyme activity of NADPH oxidase and reduced mitochondrial electron transport enzyme activities. Treatment with L-arginine via oral gavage or infusion into the cistern magna (i.c.), but not i.c. tempol or mitoQ<sub>10</sub>, significantly offset the <span style="font-variant: small-caps;">l</span>-NAME-induced hypertension in young rats. On the other hand, all treatments appreciably reduced <span style="font-variant: small-caps;">l</span>-NAME-induced hypertension in adult rats. The mRNA microarray analysis revealed that four genes involved in ROS production and clearance were differentially expressed in RVLM in an age-related manner. Of them, <i>Noxa1</i>, and <i>GPx2</i> were upregulated and <i>Duox2</i> and <i>Ucp3</i> were downregulated. Systemic <span style="font-variant: small-caps;">l</span>-NAME treatment caused greater upregulation of <i>Noxa1</i>, but not <i>Ucp3</i>, mRNA expression in RVLM of adult rats. Gene silencing of <i>Noxa1</i> in RVLM effectively alleviated oxidative stress and protected adult rats against <span style="font-variant: small-caps;">l</span>-NAME-induced hypertension. These data together suggest that hypertension induced by systemic <span style="font-variant: small-caps;">l</span>-NAME treatment in young rats is mediated primarily by NO deficiency that occurs both in vascular smooth muscle cells and RVLM. On the other hand, enhanced augmentation of oxidative stress in RVLM may contribute to the heightened susceptibility of adult rats to hypertension induced by systemic <span style="font-variant: small-caps;">l</span>-NAME treatment.https://www.mdpi.com/2227-9059/10/9/2232nitric oxide<span style="font-variant: small-caps">l</span>-NAMEhypertensionrostral ventrolateral medullaagingreactive oxygen species
spellingShingle Yung-Mei Chao
Hana Rauchová
Julie Y. H. Chan
Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in Rats
Biomedicines
nitric oxide
<span style="font-variant: small-caps">l</span>-NAME
hypertension
rostral ventrolateral medulla
aging
reactive oxygen species
title Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in Rats
title_full Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in Rats
title_fullStr Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in Rats
title_full_unstemmed Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in Rats
title_short Disparate Roles of Oxidative Stress in Rostral Ventrolateral Medulla in Age-Dependent Susceptibility to Hypertension Induced by Systemic <span style="font-variant: small-caps">l</span>-NAME Treatment in Rats
title_sort disparate roles of oxidative stress in rostral ventrolateral medulla in age dependent susceptibility to hypertension induced by systemic span style font variant small caps l span name treatment in rats
topic nitric oxide
<span style="font-variant: small-caps">l</span>-NAME
hypertension
rostral ventrolateral medulla
aging
reactive oxygen species
url https://www.mdpi.com/2227-9059/10/9/2232
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