Blood pressure, sex, and female sex hormones influence renal inner medullary nitric oxide synthase activity and expression in spontaneously hypertensive rats

We previously reported that sexually mature female spontaneously hypertensive rats (SHRs) have greater nitric oxide (NO) synthase (NOS) enzymatic activity in the renal inner medulla (IM), compared to age-matched males. However, the mechanisms responsible for this sexual dimorphism are unknown. The c...

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Veröffentlicht in:Journal of the American Heart Association 2015-04, Vol.4 (4)
Hauptverfasser: Sasser, Jennifer M, Brinson, Krystal N, Tipton, Ashlee J, Crislip, G Ryan, Sullivan, Jennifer C
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creator Sasser, Jennifer M
Brinson, Krystal N
Tipton, Ashlee J
Crislip, G Ryan
Sullivan, Jennifer C
description We previously reported that sexually mature female spontaneously hypertensive rats (SHRs) have greater nitric oxide (NO) synthase (NOS) enzymatic activity in the renal inner medulla (IM), compared to age-matched males. However, the mechanisms responsible for this sexual dimorphism are unknown. The current study tested the hypothesis that sex differences in renal IM NOS activity and NOS1 expression in adult SHRs develop with sexual maturation and increases in blood pressure (BP) in a female sex hormone-dependent manner. Renal IM were isolated from sexually immature 5-week-old and sexually mature 13-week-old male and female SHRs. Whereas NOS activity and NOS1 expression were comparable in 5- and 13-week-old male SHRs and 5-week-old female SHRs, 13-week-old females had greater NOS activity and NOS1 expression, compared to 5-week-old female SHRs and age-matched males. NOS3 expression was greater in 5-week-old than 13-week-old SHRs regardless of sex. Treatment with antihypertensive therapy (hydrochlorothiazide and reserpine) from 6 to 12 weeks of age to attenuate age-related increases in BP abolished the sex difference in NOS activity and NOS1 expression between sexually mature SHR males and females. To assess the role of female sex hormones in age-related increases in NOS, additional females were ovariectomized (OVX), and NOS activity was studied 8 weeks post-OVX. OVX decreased NOS activity and NOS1 expression. The sex difference in renal IM NOS in SHR is mediated by a sex hormone- and BP-dependent increase in NOS1 expression and NOS activity exclusively in females.
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However, the mechanisms responsible for this sexual dimorphism are unknown. The current study tested the hypothesis that sex differences in renal IM NOS activity and NOS1 expression in adult SHRs develop with sexual maturation and increases in blood pressure (BP) in a female sex hormone-dependent manner. Renal IM were isolated from sexually immature 5-week-old and sexually mature 13-week-old male and female SHRs. Whereas NOS activity and NOS1 expression were comparable in 5- and 13-week-old male SHRs and 5-week-old female SHRs, 13-week-old females had greater NOS activity and NOS1 expression, compared to 5-week-old female SHRs and age-matched males. NOS3 expression was greater in 5-week-old than 13-week-old SHRs regardless of sex. Treatment with antihypertensive therapy (hydrochlorothiazide and reserpine) from 6 to 12 weeks of age to attenuate age-related increases in BP abolished the sex difference in NOS activity and NOS1 expression between sexually mature SHR males and females. To assess the role of female sex hormones in age-related increases in NOS, additional females were ovariectomized (OVX), and NOS activity was studied 8 weeks post-OVX. OVX decreased NOS activity and NOS1 expression. 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However, the mechanisms responsible for this sexual dimorphism are unknown. The current study tested the hypothesis that sex differences in renal IM NOS activity and NOS1 expression in adult SHRs develop with sexual maturation and increases in blood pressure (BP) in a female sex hormone-dependent manner. Renal IM were isolated from sexually immature 5-week-old and sexually mature 13-week-old male and female SHRs. Whereas NOS activity and NOS1 expression were comparable in 5- and 13-week-old male SHRs and 5-week-old female SHRs, 13-week-old females had greater NOS activity and NOS1 expression, compared to 5-week-old female SHRs and age-matched males. NOS3 expression was greater in 5-week-old than 13-week-old SHRs regardless of sex. Treatment with antihypertensive therapy (hydrochlorothiazide and reserpine) from 6 to 12 weeks of age to attenuate age-related increases in BP abolished the sex difference in NOS activity and NOS1 expression between sexually mature SHR males and females. To assess the role of female sex hormones in age-related increases in NOS, additional females were ovariectomized (OVX), and NOS activity was studied 8 weeks post-OVX. OVX decreased NOS activity and NOS1 expression. The sex difference in renal IM NOS in SHR is mediated by a sex hormone- and BP-dependent increase in NOS1 expression and NOS activity exclusively in females.</description><subject>Age Factors</subject><subject>Animals</subject><subject>Antihypertensive Agents - pharmacology</subject><subject>Blood Pressure - physiology</subject><subject>Female</subject><subject>Hydrochlorothiazide - pharmacology</subject><subject>Kidney Medulla - drug effects</subject><subject>Kidney Medulla - enzymology</subject><subject>Kidney Medulla - metabolism</subject><subject>Male</subject><subject>Nitric Oxide Synthase - analysis</subject><subject>Nitric Oxide Synthase - drug effects</subject><subject>Nitric Oxide Synthase - metabolism</subject><subject>Original Research</subject><subject>Ovariectomy</subject><subject>Rats</subject><subject>Rats, Inbred SHR - metabolism</subject><subject>Rats, Inbred SHR - physiology</subject><subject>Reserpine - pharmacology</subject><subject>Sex Factors</subject><subject>Sexual Maturation - physiology</subject><issn>2047-9980</issn><issn>2047-9980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1PGzEQtVARiYAzN-QfQMBeez98qZSiUqiQeoHzyusdE1eOvbK9UfbH9L_ikBKFucwbzbz3NHoIXVFyS2lF734vH5cZ8VtCaM2aEzQvCK8XQjTk2xGeocsY_5JcVVGzUpyhWVE2GYtijv79sN73eAgQ4xjgBkfY3mDpeqxhLS3sZrzyYe0dRGyctiM4BTiAkzbPDgJeQz9aK8OEnUnBKOy3ps_MyaWVjIClSmZj0vQhC9sPL-NdZuM4eJekAz9GO-HVNEBI4KLZZAeZ4gU61dJGuPzfz9Hrw8-X-8fF859fT_fL54VigqWFrpiguiv6ogNFe15Bw2vCiYBO8rrjTVkqWkqS15XolexUpeteayZL2hS8Zufo-153GLv8jQKXgrTtEMw6v9V6adqvG2dW7ZvftLyshWBVFrjbC6jgYwygD1xK2l1Y7S6sjHi7Dyszro8tD_ef0bB39zeWfg</recordid><startdate>20150410</startdate><enddate>20150410</enddate><creator>Sasser, Jennifer M</creator><creator>Brinson, Krystal N</creator><creator>Tipton, Ashlee J</creator><creator>Crislip, G Ryan</creator><creator>Sullivan, Jennifer C</creator><general>Blackwell Publishing Ltd</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>5PM</scope></search><sort><creationdate>20150410</creationdate><title>Blood pressure, sex, and female sex hormones influence renal inner medullary nitric oxide synthase activity and expression in spontaneously hypertensive rats</title><author>Sasser, Jennifer M ; Brinson, Krystal N ; Tipton, Ashlee J ; Crislip, G Ryan ; Sullivan, Jennifer C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-f6391fb2d2bec1d46e8470409eba47b4855c15a02be69dcabc6f7dff3a5182473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Age Factors</topic><topic>Animals</topic><topic>Antihypertensive Agents - pharmacology</topic><topic>Blood Pressure - physiology</topic><topic>Female</topic><topic>Hydrochlorothiazide - pharmacology</topic><topic>Kidney Medulla - drug effects</topic><topic>Kidney Medulla - enzymology</topic><topic>Kidney Medulla - metabolism</topic><topic>Male</topic><topic>Nitric Oxide Synthase - analysis</topic><topic>Nitric Oxide Synthase - drug effects</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Original Research</topic><topic>Ovariectomy</topic><topic>Rats</topic><topic>Rats, Inbred SHR - metabolism</topic><topic>Rats, Inbred SHR - physiology</topic><topic>Reserpine - pharmacology</topic><topic>Sex Factors</topic><topic>Sexual Maturation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sasser, Jennifer M</creatorcontrib><creatorcontrib>Brinson, Krystal N</creatorcontrib><creatorcontrib>Tipton, Ashlee J</creatorcontrib><creatorcontrib>Crislip, G Ryan</creatorcontrib><creatorcontrib>Sullivan, Jennifer C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Heart Association</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sasser, Jennifer M</au><au>Brinson, Krystal N</au><au>Tipton, Ashlee J</au><au>Crislip, G Ryan</au><au>Sullivan, Jennifer C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blood pressure, sex, and female sex hormones influence renal inner medullary nitric oxide synthase activity and expression in spontaneously hypertensive rats</atitle><jtitle>Journal of the American Heart Association</jtitle><addtitle>J Am Heart Assoc</addtitle><date>2015-04-10</date><risdate>2015</risdate><volume>4</volume><issue>4</issue><issn>2047-9980</issn><eissn>2047-9980</eissn><abstract>We previously reported that sexually mature female spontaneously hypertensive rats (SHRs) have greater nitric oxide (NO) synthase (NOS) enzymatic activity in the renal inner medulla (IM), compared to age-matched males. However, the mechanisms responsible for this sexual dimorphism are unknown. The current study tested the hypothesis that sex differences in renal IM NOS activity and NOS1 expression in adult SHRs develop with sexual maturation and increases in blood pressure (BP) in a female sex hormone-dependent manner. Renal IM were isolated from sexually immature 5-week-old and sexually mature 13-week-old male and female SHRs. Whereas NOS activity and NOS1 expression were comparable in 5- and 13-week-old male SHRs and 5-week-old female SHRs, 13-week-old females had greater NOS activity and NOS1 expression, compared to 5-week-old female SHRs and age-matched males. NOS3 expression was greater in 5-week-old than 13-week-old SHRs regardless of sex. Treatment with antihypertensive therapy (hydrochlorothiazide and reserpine) from 6 to 12 weeks of age to attenuate age-related increases in BP abolished the sex difference in NOS activity and NOS1 expression between sexually mature SHR males and females. To assess the role of female sex hormones in age-related increases in NOS, additional females were ovariectomized (OVX), and NOS activity was studied 8 weeks post-OVX. OVX decreased NOS activity and NOS1 expression. The sex difference in renal IM NOS in SHR is mediated by a sex hormone- and BP-dependent increase in NOS1 expression and NOS activity exclusively in females.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25862792</pmid><doi>10.1161/JAHA.114.001738</doi><oa>free_for_read</oa></addata></record>
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subjects Age Factors
Animals
Antihypertensive Agents - pharmacology
Blood Pressure - physiology
Female
Hydrochlorothiazide - pharmacology
Kidney Medulla - drug effects
Kidney Medulla - enzymology
Kidney Medulla - metabolism
Male
Nitric Oxide Synthase - analysis
Nitric Oxide Synthase - drug effects
Nitric Oxide Synthase - metabolism
Original Research
Ovariectomy
Rats
Rats, Inbred SHR - metabolism
Rats, Inbred SHR - physiology
Reserpine - pharmacology
Sex Factors
Sexual Maturation - physiology
title Blood pressure, sex, and female sex hormones influence renal inner medullary nitric oxide synthase activity and expression in spontaneously hypertensive rats
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