Role of Brain Endothelin Receptor Type B (ETB) in the Regulation of Tyrosine Hydroxylase in the Olfactory Bulb of DOCA-Salt Hypertensive Rats.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2023-01-01 DOI:10.2174/1570161121666230622121956
Luis Cassinotti, María Guil, Liliana Bianciotti, Marcelo Vatta
{"title":"Role of Brain Endothelin Receptor Type B (ET<sub>B</sub>) in the Regulation of Tyrosine Hydroxylase in the Olfactory Bulb of DOCA-Salt Hypertensive Rats.","authors":"Luis Cassinotti,&nbsp;María Guil,&nbsp;Liliana Bianciotti,&nbsp;Marcelo Vatta","doi":"10.2174/1570161121666230622121956","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>We previously reported that endothelins (ETs) regulate tyrosine hydroxylase (TH) activity and expression in the olfactory bulb (OB) of normotensive and hypertensive animals. Applying an ET receptor type A (ET<sub>A</sub>) antagonist to the brain suggested that endogenous ETs bind to ET receptor type B (ET<sub>B</sub>) to elicit effects.</p><p><strong>Objective: </strong>The aim of the present work was to evaluate the role of central ET<sub>B</sub> stimulation on the regulation of blood pressure (BP) and the catecholaminergic system in the OB of deoxycorticosterone acetate (DOCA)-salt hypertensive rats.</p><p><strong>Methods: </strong>DOCA-salt hypertensive rats were infused for 7 days with cerebrospinal fluid or IRL-1620 (ET<sub>B</sub> receptor agonist) through a cannula placed in the lateral brain ventricle. Systolic BP (SBP) and heart rate were recorded by plethysmography. The expression of TH and its phosphorylated forms in the OB were determined by immunoblotting, TH activity by a radioenzymatic assay, and TH mRNA by quantitative real-time polymerase chain reaction.</p><p><strong>Results: </strong>Chronic administration of IRL-1620 decreased SBP in hypertensive rats but not in normotensive animals. Furthermore, the blockade of ET<sub>B</sub> receptors also decreased TH-mRNA in DOCA-salt rats, but it did not modify TH activity or protein expression.</p><p><strong>Conclusion: </strong>These findings suggest that brain ETs through the activation of ET<sub>B</sub> receptors contribute to SBP regulation in DOCA-salt hypertension. However, the catecholaminergic system in the OB does not appear to be conclusively involved although mRNA TH was reduced. Present and previous findings suggest that in this salt-sensitive animal model of hypertension, the OB contributes to chronic BP elevation.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/1570161121666230622121956","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: We previously reported that endothelins (ETs) regulate tyrosine hydroxylase (TH) activity and expression in the olfactory bulb (OB) of normotensive and hypertensive animals. Applying an ET receptor type A (ETA) antagonist to the brain suggested that endogenous ETs bind to ET receptor type B (ETB) to elicit effects.

Objective: The aim of the present work was to evaluate the role of central ETB stimulation on the regulation of blood pressure (BP) and the catecholaminergic system in the OB of deoxycorticosterone acetate (DOCA)-salt hypertensive rats.

Methods: DOCA-salt hypertensive rats were infused for 7 days with cerebrospinal fluid or IRL-1620 (ETB receptor agonist) through a cannula placed in the lateral brain ventricle. Systolic BP (SBP) and heart rate were recorded by plethysmography. The expression of TH and its phosphorylated forms in the OB were determined by immunoblotting, TH activity by a radioenzymatic assay, and TH mRNA by quantitative real-time polymerase chain reaction.

Results: Chronic administration of IRL-1620 decreased SBP in hypertensive rats but not in normotensive animals. Furthermore, the blockade of ETB receptors also decreased TH-mRNA in DOCA-salt rats, but it did not modify TH activity or protein expression.

Conclusion: These findings suggest that brain ETs through the activation of ETB receptors contribute to SBP regulation in DOCA-salt hypertension. However, the catecholaminergic system in the OB does not appear to be conclusively involved although mRNA TH was reduced. Present and previous findings suggest that in this salt-sensitive animal model of hypertension, the OB contributes to chronic BP elevation.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
脑内皮素受体B型(ETB)在DOCA盐性高血压大鼠嗅球酪氨酸羟化酶调节中的作用。
背景:我们先前报道了内皮素(ET)调节正常血压和高血压动物嗅球(OB)中酪氨酸羟化酶(TH)的活性和表达。将ET受体A型(ETA)拮抗剂应用于大脑表明,内源性ET与ET受体B型(ETB)结合以引发效应。目的:评价中枢ETB刺激对醋酸脱氧皮质酮(DOCA)盐性高血压大鼠OB血压和儿茶酚胺能系统的调节作用。方法:将脑脊液或IRL-1620(ETB受体激动剂)通过放置在侧脑室的套管输注DOCA盐性高血压大鼠7天。用体积描记法记录收缩压(SBP)和心率。TH及其磷酸化形式在OB中的表达通过免疫印迹测定,TH活性通过放射酶测定测定,TH mRNA通过定量实时聚合酶链式反应测定。结果:长期给予IRL-1620可降低高血压大鼠的SBP,但不降低血压正常的动物的SBP。此外,阻断ETB受体也降低了DOCA盐大鼠的TH mRNA,但没有改变TH活性或蛋白质表达。结论:这些发现表明,脑ETs通过激活ETB受体参与DOCA盐性高血压的SBP调节。然而,OB中的儿茶酚胺能系统似乎并没有最终参与,尽管mRNA TH减少了。目前和以前的研究结果表明,在这种对盐敏感的高血压动物模型中,OB会导致慢性血压升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊最新文献
A Systematic Review of Sleep Disturbance in Idiopathic Intracranial Hypertension. Advancing Patient Education in Idiopathic Intracranial Hypertension: The Promise of Large Language Models. Anti-Myelin-Associated Glycoprotein Neuropathy: Recent Developments. Approach to Managing the Initial Presentation of Multiple Sclerosis: A Worldwide Practice Survey. Association Between LACE+ Index Risk Category and 90-Day Mortality After Stroke.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1