Loading…
Luteolin Attenuates Hypertension via Inhibiting NF-κB-Mediated Inflammation and PI3K/Akt Signaling Pathway in the Hypothalamic Paraventricular Nucleus
Luteolin is widely distributed among a number of vegetal species worldwide. The pharmacological effects of luteolin are diverse and amongst antioxidant, free radical scavenging, and anti-inflammatory activities. Preliminary study showed that luteolin can ameliorate hypertension. However, the precise...
Saved in:
Published in: | Nutrients 2023-01, Vol.15 (3), p.502 |
---|---|
Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c539t-36551a0b4b6a7aacfafda176000daa0209d9de5fc80ed1039bc00fb86f11b833 |
---|---|
cites | cdi_FETCH-LOGICAL-c539t-36551a0b4b6a7aacfafda176000daa0209d9de5fc80ed1039bc00fb86f11b833 |
container_end_page | |
container_issue | 3 |
container_start_page | 502 |
container_title | Nutrients |
container_volume | 15 |
creator | Gao, Hong-Li Yu, Xiao-Jing Feng, Yu-Qi Yang, Yu Hu, Han-Bo Zhao, Yu-Yang Zhang, Jia-Hao Liu, Kai-Li Zhang, Yan Fu, Li-Yan Li, Ying Qi, Jie Qiao, Jin-An Kang, Yu-Ming |
description | Luteolin is widely distributed among a number of vegetal species worldwide. The pharmacological effects of luteolin are diverse and amongst antioxidant, free radical scavenging, and anti-inflammatory activities. Preliminary study showed that luteolin can ameliorate hypertension. However, the precise mechanism needs further investigation. There is no evidence that luteolin affects the paraventricular nucleus of the hypothalamus (PVN), a brain nucleus associated with a critical neural regulator of blood pressure. Our main aim was to explore the effect of luteolin on the PI3K/Akt/NF-κB signaling pathway within the PVN of hypertensive rats.
spontaneously hypertensive rats (SHRs) and corresponding normotensive control rats, the Wistar Kyoto (WKY) rats were divided into four groups and subsequently treated for 4 weeks with bilateral PVN injections of either luteolin (20 µg/0.11 µL, volume: 0.11 µL/h) or vehicle (artificial cerebrospinal fluid).
luteolin infusion to the PVN significantly decreased some hemodynamic parameters including the mean arterial pressure (MAP), heart rate (HR), circulating plasma norepinephrine (NE) and epinephrine (EPI). Additionally, there was a decrease in the expressions of the phosphatidylinositol 3-kinase (p-PI3K) and phosphorylated protein kinase-B (p-AKT), levels of reactive oxygen species (ROS), NAD(P)H oxidase subunit (NOX2, NOX4) in the PVN of SHRs. Meanwhile, the expression of inflammatory cytokines and the activity of nuclear factor κB (NF-κB) p65 in the PVN of SHRs were lowered. Furthermore, immunofluorescence results showed that injection of luteolin in the PVN reduced the expression of tyrosine hydroxylase (TH), and increased that of superoxide dismutase (SOD1) and the 67-kDa isoform of glutamate decarboxylase (GAD67) in the PVN of SHRs.
Our novel findings revealed that luteolin lowered hypertension via inhibiting NF-κB-mediated inflammation and PI3K/Akt signaling pathway in the PVN. |
doi_str_mv | 10.3390/nu15030502 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_547c721ed49e410d83f74cb1993913c0</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A743253653</galeid><doaj_id>oai_doaj_org_article_547c721ed49e410d83f74cb1993913c0</doaj_id><sourcerecordid>A743253653</sourcerecordid><originalsourceid>FETCH-LOGICAL-c539t-36551a0b4b6a7aacfafda176000daa0209d9de5fc80ed1039bc00fb86f11b833</originalsourceid><addsrcrecordid>eNptkttuEzEQhlcIRKvSGx4ArcQNQtrWXq_X8Q1SqCiNCKUSvbdmfUgcNnawvUF5Et6Fh-CZ8DalB4R94cN8849nPEXxEqMTQjg6dQOmiCCK6ifFYY1YXbVtQ54-2B8UxzGu0DgYYi15XhyQljFco_aw-Dkfkva9deU0Je0GSDqWF7uNDvkUrXfl1kI5c0vb2WTdorw8r37_el991spmVmWT6WG9hjSy4FR5NSOfTqffUvnVLhz0o88VpOUP2JU5SlrqUd6nJWQ3K7MtwFa7FKwcegjl5SB7PcQXxTMDfdTHt-tRcX3-4frsopp_-Tg7m84rSQlPFWkpxYC6pmuBAUgDRgFmbc5VAaAaccWVpkZOkFYYEd5JhEw3aQ3G3YSQo2K2l1UeVmIT7BrCTniw4ubCh4WAkGx-kqANk6zGWjVcNxipCTGskR3mnHBMJMpa7_Zam6FbayXHpKB_JPrY4uxSLPxWcF5jjGkWeHMrEPz3Qcck1jZK3ffgtB-iqBmjLW7yX2f09T_oyg8hl_uGajhFHDf31AJyAtYZn-PKUVRMWUNqmss31uDkP1SeSucP8k4bm-8fObzdO8jgYwza3OWIkRibUtw3ZYZfPazKHfq3BckfFXzdbA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2774950914</pqid></control><display><type>article</type><title>Luteolin Attenuates Hypertension via Inhibiting NF-κB-Mediated Inflammation and PI3K/Akt Signaling Pathway in the Hypothalamic Paraventricular Nucleus</title><source>Publicly Available Content (ProQuest)</source><source>PubMed Central</source><source>Coronavirus Research Database</source><creator>Gao, Hong-Li ; Yu, Xiao-Jing ; Feng, Yu-Qi ; Yang, Yu ; Hu, Han-Bo ; Zhao, Yu-Yang ; Zhang, Jia-Hao ; Liu, Kai-Li ; Zhang, Yan ; Fu, Li-Yan ; Li, Ying ; Qi, Jie ; Qiao, Jin-An ; Kang, Yu-Ming</creator><creatorcontrib>Gao, Hong-Li ; Yu, Xiao-Jing ; Feng, Yu-Qi ; Yang, Yu ; Hu, Han-Bo ; Zhao, Yu-Yang ; Zhang, Jia-Hao ; Liu, Kai-Li ; Zhang, Yan ; Fu, Li-Yan ; Li, Ying ; Qi, Jie ; Qiao, Jin-An ; Kang, Yu-Ming</creatorcontrib><description>Luteolin is widely distributed among a number of vegetal species worldwide. The pharmacological effects of luteolin are diverse and amongst antioxidant, free radical scavenging, and anti-inflammatory activities. Preliminary study showed that luteolin can ameliorate hypertension. However, the precise mechanism needs further investigation. There is no evidence that luteolin affects the paraventricular nucleus of the hypothalamus (PVN), a brain nucleus associated with a critical neural regulator of blood pressure. Our main aim was to explore the effect of luteolin on the PI3K/Akt/NF-κB signaling pathway within the PVN of hypertensive rats.
spontaneously hypertensive rats (SHRs) and corresponding normotensive control rats, the Wistar Kyoto (WKY) rats were divided into four groups and subsequently treated for 4 weeks with bilateral PVN injections of either luteolin (20 µg/0.11 µL, volume: 0.11 µL/h) or vehicle (artificial cerebrospinal fluid).
luteolin infusion to the PVN significantly decreased some hemodynamic parameters including the mean arterial pressure (MAP), heart rate (HR), circulating plasma norepinephrine (NE) and epinephrine (EPI). Additionally, there was a decrease in the expressions of the phosphatidylinositol 3-kinase (p-PI3K) and phosphorylated protein kinase-B (p-AKT), levels of reactive oxygen species (ROS), NAD(P)H oxidase subunit (NOX2, NOX4) in the PVN of SHRs. Meanwhile, the expression of inflammatory cytokines and the activity of nuclear factor κB (NF-κB) p65 in the PVN of SHRs were lowered. Furthermore, immunofluorescence results showed that injection of luteolin in the PVN reduced the expression of tyrosine hydroxylase (TH), and increased that of superoxide dismutase (SOD1) and the 67-kDa isoform of glutamate decarboxylase (GAD67) in the PVN of SHRs.
Our novel findings revealed that luteolin lowered hypertension via inhibiting NF-κB-mediated inflammation and PI3K/Akt signaling pathway in the PVN.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu15030502</identifier><identifier>PMID: 36771206</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>1-Phosphatidylinositol 3-kinase ; AKT protein ; Alzheimer's disease ; Animals ; Bioflavonoids ; Blood pressure ; Cerebrospinal fluid ; CYBB protein ; Cytokines ; Development and progression ; Diet therapy ; Epinephrine ; Flavones ; Flavonoids ; Free radicals ; Gene expression ; Glutamate decarboxylase ; Health aspects ; Heart rate ; Hemodynamics ; Hypertension ; hypothalamic paraventricular nucleus ; Hypothalamus ; Immunofluorescence ; infammatory cytokines ; Inflammation ; Inflammation - metabolism ; Kinases ; Laboratory animals ; luteolin ; Luteolin - pharmacology ; Luteolin - therapeutic use ; NAD(P)H oxidase ; NF-kappa B - metabolism ; NF-κB protein ; Norepinephrine ; NOX4 protein ; Oxidative stress ; Paraventricular Hypothalamic Nucleus - metabolism ; Paraventricular nucleus ; Phosphatidylinositol 3-Kinases - metabolism ; Physiological aspects ; PI3K/Akt/NF-κB signaling pathway ; Proto-Oncogene Proteins c-akt - metabolism ; Rats ; Rats, Inbred SHR ; Rats, Inbred WKY ; Reactive oxygen species ; Scavenging ; Signal Transduction ; Software ; Superoxide dismutase ; Sympathetic Nervous System ; Tyrosine ; Tyrosine 3-monooxygenase</subject><ispartof>Nutrients, 2023-01, Vol.15 (3), p.502</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-36551a0b4b6a7aacfafda176000daa0209d9de5fc80ed1039bc00fb86f11b833</citedby><cites>FETCH-LOGICAL-c539t-36551a0b4b6a7aacfafda176000daa0209d9de5fc80ed1039bc00fb86f11b833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2774950914/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2774950914?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74284,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36771206$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Hong-Li</creatorcontrib><creatorcontrib>Yu, Xiao-Jing</creatorcontrib><creatorcontrib>Feng, Yu-Qi</creatorcontrib><creatorcontrib>Yang, Yu</creatorcontrib><creatorcontrib>Hu, Han-Bo</creatorcontrib><creatorcontrib>Zhao, Yu-Yang</creatorcontrib><creatorcontrib>Zhang, Jia-Hao</creatorcontrib><creatorcontrib>Liu, Kai-Li</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Fu, Li-Yan</creatorcontrib><creatorcontrib>Li, Ying</creatorcontrib><creatorcontrib>Qi, Jie</creatorcontrib><creatorcontrib>Qiao, Jin-An</creatorcontrib><creatorcontrib>Kang, Yu-Ming</creatorcontrib><title>Luteolin Attenuates Hypertension via Inhibiting NF-κB-Mediated Inflammation and PI3K/Akt Signaling Pathway in the Hypothalamic Paraventricular Nucleus</title><title>Nutrients</title><addtitle>Nutrients</addtitle><description>Luteolin is widely distributed among a number of vegetal species worldwide. The pharmacological effects of luteolin are diverse and amongst antioxidant, free radical scavenging, and anti-inflammatory activities. Preliminary study showed that luteolin can ameliorate hypertension. However, the precise mechanism needs further investigation. There is no evidence that luteolin affects the paraventricular nucleus of the hypothalamus (PVN), a brain nucleus associated with a critical neural regulator of blood pressure. Our main aim was to explore the effect of luteolin on the PI3K/Akt/NF-κB signaling pathway within the PVN of hypertensive rats.
spontaneously hypertensive rats (SHRs) and corresponding normotensive control rats, the Wistar Kyoto (WKY) rats were divided into four groups and subsequently treated for 4 weeks with bilateral PVN injections of either luteolin (20 µg/0.11 µL, volume: 0.11 µL/h) or vehicle (artificial cerebrospinal fluid).
luteolin infusion to the PVN significantly decreased some hemodynamic parameters including the mean arterial pressure (MAP), heart rate (HR), circulating plasma norepinephrine (NE) and epinephrine (EPI). Additionally, there was a decrease in the expressions of the phosphatidylinositol 3-kinase (p-PI3K) and phosphorylated protein kinase-B (p-AKT), levels of reactive oxygen species (ROS), NAD(P)H oxidase subunit (NOX2, NOX4) in the PVN of SHRs. Meanwhile, the expression of inflammatory cytokines and the activity of nuclear factor κB (NF-κB) p65 in the PVN of SHRs were lowered. Furthermore, immunofluorescence results showed that injection of luteolin in the PVN reduced the expression of tyrosine hydroxylase (TH), and increased that of superoxide dismutase (SOD1) and the 67-kDa isoform of glutamate decarboxylase (GAD67) in the PVN of SHRs.
Our novel findings revealed that luteolin lowered hypertension via inhibiting NF-κB-mediated inflammation and PI3K/Akt signaling pathway in the PVN.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>AKT protein</subject><subject>Alzheimer's disease</subject><subject>Animals</subject><subject>Bioflavonoids</subject><subject>Blood pressure</subject><subject>Cerebrospinal fluid</subject><subject>CYBB protein</subject><subject>Cytokines</subject><subject>Development and progression</subject><subject>Diet therapy</subject><subject>Epinephrine</subject><subject>Flavones</subject><subject>Flavonoids</subject><subject>Free radicals</subject><subject>Gene expression</subject><subject>Glutamate decarboxylase</subject><subject>Health aspects</subject><subject>Heart rate</subject><subject>Hemodynamics</subject><subject>Hypertension</subject><subject>hypothalamic paraventricular nucleus</subject><subject>Hypothalamus</subject><subject>Immunofluorescence</subject><subject>infammatory cytokines</subject><subject>Inflammation</subject><subject>Inflammation - metabolism</subject><subject>Kinases</subject><subject>Laboratory animals</subject><subject>luteolin</subject><subject>Luteolin - pharmacology</subject><subject>Luteolin - therapeutic use</subject><subject>NAD(P)H oxidase</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB protein</subject><subject>Norepinephrine</subject><subject>NOX4 protein</subject><subject>Oxidative stress</subject><subject>Paraventricular Hypothalamic Nucleus - metabolism</subject><subject>Paraventricular nucleus</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Physiological aspects</subject><subject>PI3K/Akt/NF-κB signaling pathway</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Inbred WKY</subject><subject>Reactive oxygen species</subject><subject>Scavenging</subject><subject>Signal Transduction</subject><subject>Software</subject><subject>Superoxide dismutase</subject><subject>Sympathetic Nervous System</subject><subject>Tyrosine</subject><subject>Tyrosine 3-monooxygenase</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkttuEzEQhlcIRKvSGx4ArcQNQtrWXq_X8Q1SqCiNCKUSvbdmfUgcNnawvUF5Et6Fh-CZ8DalB4R94cN8849nPEXxEqMTQjg6dQOmiCCK6ifFYY1YXbVtQ54-2B8UxzGu0DgYYi15XhyQljFco_aw-Dkfkva9deU0Je0GSDqWF7uNDvkUrXfl1kI5c0vb2WTdorw8r37_el991spmVmWT6WG9hjSy4FR5NSOfTqffUvnVLhz0o88VpOUP2JU5SlrqUd6nJWQ3K7MtwFa7FKwcegjl5SB7PcQXxTMDfdTHt-tRcX3-4frsopp_-Tg7m84rSQlPFWkpxYC6pmuBAUgDRgFmbc5VAaAaccWVpkZOkFYYEd5JhEw3aQ3G3YSQo2K2l1UeVmIT7BrCTniw4ubCh4WAkGx-kqANk6zGWjVcNxipCTGskR3mnHBMJMpa7_Zam6FbayXHpKB_JPrY4uxSLPxWcF5jjGkWeHMrEPz3Qcck1jZK3ffgtB-iqBmjLW7yX2f09T_oyg8hl_uGajhFHDf31AJyAtYZn-PKUVRMWUNqmss31uDkP1SeSucP8k4bm-8fObzdO8jgYwza3OWIkRibUtw3ZYZfPazKHfq3BckfFXzdbA</recordid><startdate>20230118</startdate><enddate>20230118</enddate><creator>Gao, Hong-Li</creator><creator>Yu, Xiao-Jing</creator><creator>Feng, Yu-Qi</creator><creator>Yang, Yu</creator><creator>Hu, Han-Bo</creator><creator>Zhao, Yu-Yang</creator><creator>Zhang, Jia-Hao</creator><creator>Liu, Kai-Li</creator><creator>Zhang, Yan</creator><creator>Fu, Li-Yan</creator><creator>Li, Ying</creator><creator>Qi, Jie</creator><creator>Qiao, Jin-An</creator><creator>Kang, Yu-Ming</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230118</creationdate><title>Luteolin Attenuates Hypertension via Inhibiting NF-κB-Mediated Inflammation and PI3K/Akt Signaling Pathway in the Hypothalamic Paraventricular Nucleus</title><author>Gao, Hong-Li ; Yu, Xiao-Jing ; Feng, Yu-Qi ; Yang, Yu ; Hu, Han-Bo ; Zhao, Yu-Yang ; Zhang, Jia-Hao ; Liu, Kai-Li ; Zhang, Yan ; Fu, Li-Yan ; Li, Ying ; Qi, Jie ; Qiao, Jin-An ; Kang, Yu-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-36551a0b4b6a7aacfafda176000daa0209d9de5fc80ed1039bc00fb86f11b833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>AKT protein</topic><topic>Alzheimer's disease</topic><topic>Animals</topic><topic>Bioflavonoids</topic><topic>Blood pressure</topic><topic>Cerebrospinal fluid</topic><topic>CYBB protein</topic><topic>Cytokines</topic><topic>Development and progression</topic><topic>Diet therapy</topic><topic>Epinephrine</topic><topic>Flavones</topic><topic>Flavonoids</topic><topic>Free radicals</topic><topic>Gene expression</topic><topic>Glutamate decarboxylase</topic><topic>Health aspects</topic><topic>Heart rate</topic><topic>Hemodynamics</topic><topic>Hypertension</topic><topic>hypothalamic paraventricular nucleus</topic><topic>Hypothalamus</topic><topic>Immunofluorescence</topic><topic>infammatory cytokines</topic><topic>Inflammation</topic><topic>Inflammation - metabolism</topic><topic>Kinases</topic><topic>Laboratory animals</topic><topic>luteolin</topic><topic>Luteolin - pharmacology</topic><topic>Luteolin - therapeutic use</topic><topic>NAD(P)H oxidase</topic><topic>NF-kappa B - metabolism</topic><topic>NF-κB protein</topic><topic>Norepinephrine</topic><topic>NOX4 protein</topic><topic>Oxidative stress</topic><topic>Paraventricular Hypothalamic Nucleus - metabolism</topic><topic>Paraventricular nucleus</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>Physiological aspects</topic><topic>PI3K/Akt/NF-κB signaling pathway</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Inbred WKY</topic><topic>Reactive oxygen species</topic><topic>Scavenging</topic><topic>Signal Transduction</topic><topic>Software</topic><topic>Superoxide dismutase</topic><topic>Sympathetic Nervous System</topic><topic>Tyrosine</topic><topic>Tyrosine 3-monooxygenase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Hong-Li</creatorcontrib><creatorcontrib>Yu, Xiao-Jing</creatorcontrib><creatorcontrib>Feng, Yu-Qi</creatorcontrib><creatorcontrib>Yang, Yu</creatorcontrib><creatorcontrib>Hu, Han-Bo</creatorcontrib><creatorcontrib>Zhao, Yu-Yang</creatorcontrib><creatorcontrib>Zhang, Jia-Hao</creatorcontrib><creatorcontrib>Liu, Kai-Li</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Fu, Li-Yan</creatorcontrib><creatorcontrib>Li, Ying</creatorcontrib><creatorcontrib>Qi, Jie</creatorcontrib><creatorcontrib>Qiao, Jin-An</creatorcontrib><creatorcontrib>Kang, Yu-Ming</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Nutrients</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Hong-Li</au><au>Yu, Xiao-Jing</au><au>Feng, Yu-Qi</au><au>Yang, Yu</au><au>Hu, Han-Bo</au><au>Zhao, Yu-Yang</au><au>Zhang, Jia-Hao</au><au>Liu, Kai-Li</au><au>Zhang, Yan</au><au>Fu, Li-Yan</au><au>Li, Ying</au><au>Qi, Jie</au><au>Qiao, Jin-An</au><au>Kang, Yu-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Luteolin Attenuates Hypertension via Inhibiting NF-κB-Mediated Inflammation and PI3K/Akt Signaling Pathway in the Hypothalamic Paraventricular Nucleus</atitle><jtitle>Nutrients</jtitle><addtitle>Nutrients</addtitle><date>2023-01-18</date><risdate>2023</risdate><volume>15</volume><issue>3</issue><spage>502</spage><pages>502-</pages><issn>2072-6643</issn><eissn>2072-6643</eissn><abstract>Luteolin is widely distributed among a number of vegetal species worldwide. The pharmacological effects of luteolin are diverse and amongst antioxidant, free radical scavenging, and anti-inflammatory activities. Preliminary study showed that luteolin can ameliorate hypertension. However, the precise mechanism needs further investigation. There is no evidence that luteolin affects the paraventricular nucleus of the hypothalamus (PVN), a brain nucleus associated with a critical neural regulator of blood pressure. Our main aim was to explore the effect of luteolin on the PI3K/Akt/NF-κB signaling pathway within the PVN of hypertensive rats.
spontaneously hypertensive rats (SHRs) and corresponding normotensive control rats, the Wistar Kyoto (WKY) rats were divided into four groups and subsequently treated for 4 weeks with bilateral PVN injections of either luteolin (20 µg/0.11 µL, volume: 0.11 µL/h) or vehicle (artificial cerebrospinal fluid).
luteolin infusion to the PVN significantly decreased some hemodynamic parameters including the mean arterial pressure (MAP), heart rate (HR), circulating plasma norepinephrine (NE) and epinephrine (EPI). Additionally, there was a decrease in the expressions of the phosphatidylinositol 3-kinase (p-PI3K) and phosphorylated protein kinase-B (p-AKT), levels of reactive oxygen species (ROS), NAD(P)H oxidase subunit (NOX2, NOX4) in the PVN of SHRs. Meanwhile, the expression of inflammatory cytokines and the activity of nuclear factor κB (NF-κB) p65 in the PVN of SHRs were lowered. Furthermore, immunofluorescence results showed that injection of luteolin in the PVN reduced the expression of tyrosine hydroxylase (TH), and increased that of superoxide dismutase (SOD1) and the 67-kDa isoform of glutamate decarboxylase (GAD67) in the PVN of SHRs.
Our novel findings revealed that luteolin lowered hypertension via inhibiting NF-κB-mediated inflammation and PI3K/Akt signaling pathway in the PVN.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36771206</pmid><doi>10.3390/nu15030502</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2072-6643 |
ispartof | Nutrients, 2023-01, Vol.15 (3), p.502 |
issn | 2072-6643 2072-6643 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_547c721ed49e410d83f74cb1993913c0 |
source | Publicly Available Content (ProQuest); PubMed Central; Coronavirus Research Database |
subjects | 1-Phosphatidylinositol 3-kinase AKT protein Alzheimer's disease Animals Bioflavonoids Blood pressure Cerebrospinal fluid CYBB protein Cytokines Development and progression Diet therapy Epinephrine Flavones Flavonoids Free radicals Gene expression Glutamate decarboxylase Health aspects Heart rate Hemodynamics Hypertension hypothalamic paraventricular nucleus Hypothalamus Immunofluorescence infammatory cytokines Inflammation Inflammation - metabolism Kinases Laboratory animals luteolin Luteolin - pharmacology Luteolin - therapeutic use NAD(P)H oxidase NF-kappa B - metabolism NF-κB protein Norepinephrine NOX4 protein Oxidative stress Paraventricular Hypothalamic Nucleus - metabolism Paraventricular nucleus Phosphatidylinositol 3-Kinases - metabolism Physiological aspects PI3K/Akt/NF-κB signaling pathway Proto-Oncogene Proteins c-akt - metabolism Rats Rats, Inbred SHR Rats, Inbred WKY Reactive oxygen species Scavenging Signal Transduction Software Superoxide dismutase Sympathetic Nervous System Tyrosine Tyrosine 3-monooxygenase |
title | Luteolin Attenuates Hypertension via Inhibiting NF-κB-Mediated Inflammation and PI3K/Akt Signaling Pathway in the Hypothalamic Paraventricular Nucleus |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T00%3A36%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Luteolin%20Attenuates%20Hypertension%20via%20Inhibiting%20NF-%CE%BAB-Mediated%20Inflammation%20and%20PI3K/Akt%20Signaling%20Pathway%20in%20the%20Hypothalamic%20Paraventricular%20Nucleus&rft.jtitle=Nutrients&rft.au=Gao,%20Hong-Li&rft.date=2023-01-18&rft.volume=15&rft.issue=3&rft.spage=502&rft.pages=502-&rft.issn=2072-6643&rft.eissn=2072-6643&rft_id=info:doi/10.3390/nu15030502&rft_dat=%3Cgale_doaj_%3EA743253653%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c539t-36551a0b4b6a7aacfafda176000daa0209d9de5fc80ed1039bc00fb86f11b833%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2774950914&rft_id=info:pmid/36771206&rft_galeid=A743253653&rfr_iscdi=true |