The ductus arteriosus (DA) is dilated in the hypoxic environment of the developing fetus. At birth the DA constricts in response to normoxia. In contrast, the pulmonary artery (PA) is dilated in normoxia and constricts in hypoxia. Although their responses to oxygen tension (pO2) are opposite, both vascular tissues have O2-sensitive ion channels in their smooth muscle cells (SMC). We have shown that O2-sensitive K+ channels are partly responsible for these opposing effects of pO2 in these two smooth muscle ceil types. We have performed experiments indicating the existence of additional pO2-sensitive mechanisms in DA SMCs. Specifically, we hypothesize that 1. DASMCs, like PASMCs, have store-operated channels (SOCs) and they play an important role in normoxic vasoconstriction. 2. An acute rise in pO2 initiates calcium influx via SOCs in the DA while an acute fall in pO2 does the same in the PA. 3. Longer-term changes in pO2 alters the level of expression of SOCs in DA and PA SMCs before structural remodeling of vessels occurs. 4. Calcium sensitivity modulates the effect of pO2-mediated SMC cytosolic calcium changes on DA and PA vasoconstriction. Our studies will use molecular biology techniques including RNA interference to determine the identities of SOCs involved in pO2-mediated vasoconstriction in DA and PA. The effects of changes in pO2 on SOC activity in DA and PA smooth muscle cells will be determined using patch-clamp techniques. Changes in [Ca2+]i in response to altering pO2 will be recorded using single-cell Ca2+ imaging techniques. Calcium sensitivity will be assessed by measuring Rho/Rho-kinase activity and by performing b-escin-permeabilized DA and PA ring experiments to control [Ca2+]i. Persistent patent ductus is a common congenital defect in newborns and treatment of pulmonary hypertension is extremely limited. A better understanding of the mechanisms of O2-mediated changes in tone in the ductus arteriosus and pulmonary artery would therefore be of significant medical importance.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL065322-07
Application #
7386762
Study Section
Pregnancy and Neonatology Study Section (PN)
Program Officer
Schramm, Charlene A
Project Start
2000-07-01
Project End
2009-12-31
Budget Start
2008-04-01
Budget End
2009-12-31
Support Year
7
Fiscal Year
2008
Total Cost
$305,865
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Hong, Zhigang; Cabrera, Jésus A; Mahapatra, Saswati et al. (2014) Activation of the EGFR/p38/JNK pathway by mitochondrial-derived hydrogen peroxide contributes to oxygen-induced contraction of ductus arteriosus. J Mol Med (Berl) 92:995-1007
Nagaraj, Chandran; Tang, Bi; Balint, Zoltan et al. (2013) Src tyrosine kinase is crucial for potassium channel function in human pulmonary arteries. Eur Respir J 41:85-95
Chen, Yingjie; Guo, Haipeng; Xu, Dachun et al. (2012) Left ventricular failure produces profound lung remodeling and pulmonary hypertension in mice: heart failure causes severe lung disease. Hypertension 59:1170-8
Xu, Dachun; Guo, Haipeng; Xu, Xin et al. (2011) Exacerbated pulmonary arterial hypertension and right ventricular hypertrophy in animals with loss of function of extracellular superoxide dismutase. Hypertension 58:303-9
Adhikari, Neeta; Basi, David L; Carlson, Marjorie et al. (2011) Increase in GLUT1 in smooth muscle alters vascular contractility and increases inflammation in response to vascular injury. Arterioscler Thromb Vasc Biol 31:86-94
Weir, E Kenneth; Cabrera, Jésus A; Mahapatra, Saswati et al. (2010) The role of ion channels in hypoxic pulmonary vasoconstriction. Adv Exp Med Biol 661:3-14
Weir, E Kenneth; Archer, Stephen L (2010) The role of redox changes in oxygen sensing. Respir Physiol Neurobiol 174:182-91
Archer, Stephen L; Weir, E Kenneth; Wilkins, Martin R (2010) Basic science of pulmonary arterial hypertension for clinicians: new concepts and experimental therapies. Circulation 121:2045-66
Weir, E K; Hong, Z; Chen, Y (2010) Superoxide dismutase: master and commander? Eur Respir J 36:234-6
Morrell, Nicholas W; Adnot, Serge; Archer, Stephen L et al. (2009) Cellular and molecular basis of pulmonary arterial hypertension. J Am Coll Cardiol 54:S20-31

Showing the most recent 10 out of 38 publications