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1.
Am J Physiol Regul Integr Comp Physiol ; 314(3): R433-R446, 2018 03 01.
Article in English | MEDLINE | ID: mdl-29167165

ABSTRACT

Long-term hypoxia (LTH) has a profound effect on pulmonary arterial vasoconstriction in the fetus and adult. Dysregulation in Ca2+ signaling is important during the development of LTH-induced pulmonary hypertension. In the present study, we tested the hypothesis that L-type Ca2+ channels (CaL), which are voltage dependent and found in smooth, skeletal, and cardiac muscle, are important in the adaptation of pulmonary arterial contractions in postnatal maturation and in response to LTH. Pulmonary arteries were isolated from fetal or adult sheep maintained at low or high altitude (3,801 m) for >100 days. The effects were measured using an L-type Ca2+ channel opener FPL 64176 (FPL) in the presence or absence of an inhibitor, Nifedipine (NIF) on arterial contractions, intracellular Ca2+ oscillations, and ryanodine receptor-driven Ca2+ sparks. FPL induced pulmonary arterial contractions in all groups were sensitive to NIF. However, when compared with 125 mM K+, FPL contractions were greater in fetuses than in adults. FPL reduced Ca2+ oscillations in myocytes of adult but not fetal arteries, independently of altitude. The FPL effects on Ca2+ oscillations were reversed by NIF in myocytes of hypoxic but not normoxic adults. FPL failed to enhance Ca2+ spark frequency and had little impact on spatiotemporal firing characteristics. These data suggest that CaL-dependent contractions are largely uncoupled from intracellular Ca2+ oscillations and the development of Ca2+ sparks. This raises questions regarding the coupling of pulmonary arterial contractility to membrane depolarization, attendant CaL facilitation, and the related associations with the activation of Ca2+ oscillations and Ca2+ sparks.


Subject(s)
Altitude Sickness/metabolism , Calcium Channels, L-Type/metabolism , Calcium Signaling , Calcium/metabolism , Pulmonary Artery/metabolism , Vasoconstriction , Altitude Sickness/physiopathology , Animals , Calcium Channel Agonists/pharmacology , Calcium Channel Blockers/pharmacology , Calcium Channels, L-Type/drug effects , Calcium Signaling/drug effects , Disease Models, Animal , Female , Fetal Heart/metabolism , Fetal Heart/physiopathology , Gestational Age , Membrane Potentials , Myocytes, Cardiac/metabolism , Pregnancy , Pulmonary Artery/drug effects , Pulmonary Artery/embryology , Pulmonary Artery/physiopathology , Sheep, Domestic , Time Factors , Vasoconstriction/drug effects
2.
Pediatr Res ; 79(3): 432-7, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26539663

ABSTRACT

BACKGROUND: Plasma nitrite serves as a reservoir of nitric oxide (NO) bioactivity. Because nitrite ingestion is markedly lower in newborns than adults, we hypothesized plasma nitrite levels would be lower in newborns than in adults, and that infants diagnosed with necrotizing enterocolitis (NEC), a disease characterized by ischemia and bacterial invasion of intestinal walls, would have lower levels of circulating nitrite in the days prior to diagnosis. METHODS: Single blood and urine samples were collected from 9 term infants and 12 adults, 72 preterm infants every 5 d for 3 wk, and from 13 lambs before and after cord occlusion. RESULTS: Nitrite fell 50% relative to cord levels in the first day after birth; and within 15 min after cord occlusion in lambs. Urinary nitrite was higher in infants than adults. Plasma and urinary nitrite levels in infants who developed NEC were similar to those of preterm control infants on days 1 and 5, but significantly elevated at 15 and 20 d after birth. CONCLUSION: Plasma nitrite falls dramatically at birth while newborn urinary nitrite levels are significantly greater than adults. Acute NEC is associated with elevated plasma and urinary nitrite levels.


Subject(s)
Enterocolitis, Necrotizing/blood , Enterocolitis, Necrotizing/urine , Nitrites/blood , Nitrites/urine , Adult , Animals , Case-Control Studies , Female , Humans , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/blood , Male , Nitrates/blood , Nitric Oxide , Pregnancy , Pregnancy, Animal , Sheep
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