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However, the involvement of tachykinin receptors (<jats:styled-content style=\"fixed-case\">NKR<\/jats:styled-content>s) within baroreflex afferent pathway in <jats:styled-content style=\"fixed-case\">SP<\/jats:styled-content>\u2010mediated <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content> regulation is largely unknown.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Under control and hypertensive condition, <jats:styled-content style=\"fixed-case\">NKR<\/jats:styled-content>s\u2019 expressions were evaluated in nodose (<jats:styled-content style=\"fixed-case\">NG<\/jats:styled-content>) and nucleus of tractus solitary (<jats:styled-content style=\"fixed-case\">NTS<\/jats:styled-content>) of male, female, and ovariectomized (<jats:styled-content style=\"fixed-case\">OVX<\/jats:styled-content>) rats; <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content> was recorded after microinjection of <jats:styled-content style=\"fixed-case\">SP<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">NKR<\/jats:styled-content>s agonists into <jats:styled-content style=\"fixed-case\">NG<\/jats:styled-content>; Baroreceptor sensitivity (<jats:styled-content style=\"fixed-case\">BRS<\/jats:styled-content>) was tested as well.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Immunostaining and immunoblotting data showed that <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>1R and <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>2R were estrogen\u2010dependently expressed on myelinated and unmyelinated afferents in <jats:styled-content style=\"fixed-case\">NG<\/jats:styled-content>. A functional study showed that <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content> was reduced dose\u2010dependently by <jats:styled-content style=\"fixed-case\">SP<\/jats:styled-content> microinjection, which was more dramatic in males and can be mimicked by <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>1R and <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>2R agonists. Notably, further <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content> elevation and <jats:styled-content style=\"fixed-case\">BRS<\/jats:styled-content> dysfunction were confirmed in desoxycorticosterone acetate (<jats:styled-content style=\"fixed-case\">DOCA<\/jats:styled-content>)\u2010salt model in <jats:styled-content style=\"fixed-case\">OVX<\/jats:styled-content> compared with <jats:styled-content style=\"fixed-case\">DOCA<\/jats:styled-content>\u2010salt model in intact female rats. Additionally, similar changes in <jats:styled-content style=\"fixed-case\">NKR<\/jats:styled-content>s\u2019 expression in <jats:styled-content style=\"fixed-case\">NG<\/jats:styled-content> were also detected using <jats:styled-content style=\"fixed-case\">DOCA<\/jats:styled-content>\u2010salt and <jats:styled-content style=\"fixed-case\">SHR<\/jats:styled-content>. Compared with <jats:styled-content style=\"fixed-case\">NG<\/jats:styled-content>, inversed expression profiles of <jats:styled-content style=\"fixed-case\">NKR<\/jats:styled-content>s were also found in <jats:styled-content style=\"fixed-case\">NTS<\/jats:styled-content> with either gender.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The estrogen\u2010dependent <jats:styled-content style=\"fixed-case\">NKR<\/jats:styled-content>s\u2019 expression in baroreflex afferent pathway participates at least partially in sexual\u2010dimorphic and <jats:styled-content style=\"fixed-case\">SP<\/jats:styled-content>\u2010mediated <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content> regulation under physiological and hypertensive 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