Impaired pulmonary artery contractile responses in a rat model of microgravity: Role of nitric oxide

Daniel Nyhan, Soonyul Kim, Stacey Dunbar, Dechun Li, Artin Shoukas, Dan E. Berkowitz

Research output: Contribution to journalArticlepeer-review

Abstract

Vascular contractile hyporesponsiveness is an important mechanism underlying orthostatic intolerance after microgravity. Baroreceptor reflexes can modulate both pulmonary resistance and capacitance function and thus cardiac output. We hypothesized, therefore, that pulmonary vasoreactivity is impaired in the hindlimb-unweighted (HLU) rat model of microgravity. Pulmonary artery (PA) contractile responses to phenylephrine (PE) and U-46619 (U4) were significantly decreased in the PAs from HLU vs. control (C) animals. NGnitro-L-arginine methyl ester (10-5 M) enhanced the contractile responses in the PA rings from both C and HLU animals and completely abolished the differential responses to PE and U4 in HLU vs. C animals. Vasorelaxant responses to ACh were significantly enhanced in PA rings from HLU rats compared with C. Moreover, vasorelaxant responses to sodium nitroprusside were also significantly enhanced. Endothelial nitric oxide synthase (eNOS) and soluble guanlyl cyclase expression were significantly enhanced in PA and lung tissue from HLU rats. In marked contrast, the expression of inducible nitric oxide synthase was unchanged in lung tissue. These data support the hypothesis that vascular contractile responsiveness is attenuated in PAs from HLU rats and that this hyporesponsiveness is due at least in part to increased nitric oxide synthase activity resulting from enhanced eNOS expression. These findings may have important implications for blood volume distribution and attenuated stroke volume responses to orthostatic stress after microgravity exposure.

Original languageEnglish (US)
Pages (from-to)33-40
Number of pages8
JournalJournal of applied physiology
Volume92
Issue number1
DOIs
StatePublished - 2002

Keywords

  • Endothelium
  • Hindlimb unweighting
  • Nitric oxide synthase
  • Orthostatic intolerance
  • Vasodilation

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)

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