Id) and Howard Hughes Medical Institute Medical Research Fellows Program (Anbil) is gratefully acknowledged. The authors would like to acknowledge Mr. Brian Battersby, Director of Computational Core, Wellman Center for Photomedicine for the help with cover art.Competing InterestsThe authors have Doravirine web declared that no competing interest exists.
J Physiol 590.15 (2012) pp 3545?Decreased expression of trans-4-HydroxytamoxifenMedChemExpress trans-4-Hydroxytamoxifen neuronal nitric oxide synthase in the nucleus tractus solitarii inhibits sympathetically mediated baroreflex responses in ratLi-Hsien Lin1 , Deidre Nitschke Dragon1 , Jingwen Jin1 , Xin Tian2 , Yi Chu2 , Curt Sigmund2 and William T. Talman1,1Laboratory of Neurobiology, Department of Neurology, Roy and Lucille Carver College of Medicine, University of Iowa, Iowa City, IA, USA Department of Internal Medicine and Pharmacology, Roy and Lucille Carver College of Medicine, University of Iowa, Iowa City, IA, USA 3 Neurology Service, Department of Veterans Affairs Medical Center, Iowa City, IA, USAKey pointsThe Journal of Physiology?Arteries send nerve signals to the brain in response to changes in blood pressure. ?Nerves carrying these signals release chemical transmitters onto other neurons in the nucleus ?One chemical that has been considered such a transmitter is nitric oxide, but there has beentractus solitarii, a nucleus in the brainstem.debate over the action of nitric oxide in brainstem influences on responses to changes blood pressure. ?We show that use of a molecular tool that allows us to prevent the normal production of nitric oxide by nerve cells leads to altered reflex regulation of heart rate in rats. ?Our findings, which clarify the role of neuronally derived nitric oxide in control of the cardiovascular system by the brain, could lead to better control of blood pressure in individuals with either high or low blood pressure.Abstract Despite numerous studies it remains controversial whether nitric oxide (NO? synthesized by neuronal NOS (nNOS) plays an excitatory or inhibitory role in transmission of baroreflex signals in the nucleus tractus solitarii (NTS). In the current studies we sought to test the hypothesis that nNOS is involved in excitation of baroreflex pathways in NTS while excluding pharmacological interventions in assessing the influence of nNOS. We therefore developed, validated and utilized a short hairpin RNA (shRNA) to reduce expression of nNOS in the NTS of rats whose baroreflex activity was then studied. We demonstrate downregulation of nNOS through transduction with adeno-associated virus type 2 (AAV2) carrying shRNA for nNOS. When injected bilaterally into NTS AAV2nNOSshRNA significantly reduced reflex tachycardic responses to acute hypotension while not affecting reflex bradycardic responses to acute increases of arterial pressure. Control animals treated with intravenous propranolol to block sympathetically mediated chronotropic responses manifested the same baroreflex responses as animals that had been treated with AAV2nNOSshRNA. Neither AAV2 eGFP nor AAV2nNOScDNA affected baroreflex responses. Blocking cardiac vagal influences with atropine similarly reduced baroreflex-mediated bradycardic responses to increases in arterial pressure both in control animals and in those treated with AAV2nNOSshRNA. We conclude that NO?synthesized by nNOS in the NTS is integral to excitation of baroreflex pathways involved in reflex tachycardia, a largely sympathetically mediated response, but not reflex bradycardia, a largely parasympath.Id) and Howard Hughes Medical Institute Medical Research Fellows Program (Anbil) is gratefully acknowledged. The authors would like to acknowledge Mr. Brian Battersby, Director of Computational Core, Wellman Center for Photomedicine for the help with cover art.Competing InterestsThe authors have declared that no competing interest exists.
J Physiol 590.15 (2012) pp 3545?Decreased expression of neuronal nitric oxide synthase in the nucleus tractus solitarii inhibits sympathetically mediated baroreflex responses in ratLi-Hsien Lin1 , Deidre Nitschke Dragon1 , Jingwen Jin1 , Xin Tian2 , Yi Chu2 , Curt Sigmund2 and William T. Talman1,1Laboratory of Neurobiology, Department of Neurology, Roy and Lucille Carver College of Medicine, University of Iowa, Iowa City, IA, USA Department of Internal Medicine and Pharmacology, Roy and Lucille Carver College of Medicine, University of Iowa, Iowa City, IA, USA 3 Neurology Service, Department of Veterans Affairs Medical Center, Iowa City, IA, USAKey pointsThe Journal of Physiology?Arteries send nerve signals to the brain in response to changes in blood pressure. ?Nerves carrying these signals release chemical transmitters onto other neurons in the nucleus ?One chemical that has been considered such a transmitter is nitric oxide, but there has beentractus solitarii, a nucleus in the brainstem.debate over the action of nitric oxide in brainstem influences on responses to changes blood pressure. ?We show that use of a molecular tool that allows us to prevent the normal production of nitric oxide by nerve cells leads to altered reflex regulation of heart rate in rats. ?Our findings, which clarify the role of neuronally derived nitric oxide in control of the cardiovascular system by the brain, could lead to better control of blood pressure in individuals with either high or low blood pressure.Abstract Despite numerous studies it remains controversial whether nitric oxide (NO? synthesized by neuronal NOS (nNOS) plays an excitatory or inhibitory role in transmission of baroreflex signals in the nucleus tractus solitarii (NTS). In the current studies we sought to test the hypothesis that nNOS is involved in excitation of baroreflex pathways in NTS while excluding pharmacological interventions in assessing the influence of nNOS. We therefore developed, validated and utilized a short hairpin RNA (shRNA) to reduce expression of nNOS in the NTS of rats whose baroreflex activity was then studied. We demonstrate downregulation of nNOS through transduction with adeno-associated virus type 2 (AAV2) carrying shRNA for nNOS. When injected bilaterally into NTS AAV2nNOSshRNA significantly reduced reflex tachycardic responses to acute hypotension while not affecting reflex bradycardic responses to acute increases of arterial pressure. Control animals treated with intravenous propranolol to block sympathetically mediated chronotropic responses manifested the same baroreflex responses as animals that had been treated with AAV2nNOSshRNA. Neither AAV2 eGFP nor AAV2nNOScDNA affected baroreflex responses. Blocking cardiac vagal influences with atropine similarly reduced baroreflex-mediated bradycardic responses to increases in arterial pressure both in control animals and in those treated with AAV2nNOSshRNA. We conclude that NO?synthesized by nNOS in the NTS is integral to excitation of baroreflex pathways involved in reflex tachycardia, a largely sympathetically mediated response, but not reflex bradycardia, a largely parasympath.