Intra-Amniotic Sildenafil and Rosiglitazone Late in Gestation Ameliorate the Pulmonary Hypertension Phenotype in Congenital Diaphragmatic Hernia

Pulmonary hypertension remains difficult to manage in congenital diaphragmatic hernia (CDH). Prenatal therapy may ameliorate postnatal pulmonary hypertension. We hypothesized that intra-amniotic (IA) injection of either sildenafil, a phosphodiesterase 5 inhibitor, or rosiglitazone, a PPAR-γ agonist,...

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Veröffentlicht in:Journal of pediatric surgery 2024-08, Vol.59 (8), p.1515-1525
Hauptverfasser: Yoshida, Shiho, Eichelberger, Olivia, Ulis, Michael, Kreger, Alexander M., Gittes, George K., Church, Joseph T.
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container_end_page 1525
container_issue 8
container_start_page 1515
container_title Journal of pediatric surgery
container_volume 59
creator Yoshida, Shiho
Eichelberger, Olivia
Ulis, Michael
Kreger, Alexander M.
Gittes, George K.
Church, Joseph T.
description Pulmonary hypertension remains difficult to manage in congenital diaphragmatic hernia (CDH). Prenatal therapy may ameliorate postnatal pulmonary hypertension. We hypothesized that intra-amniotic (IA) injection of either sildenafil, a phosphodiesterase 5 inhibitor, or rosiglitazone, a PPAR-γ agonist, or both late in gestation would decrease the detrimental pulmonary vascular remodeling seen in CDH and improve peripheral pulmonary blood flow. Pregnant rats were gavaged with nitrogen on embryonic day (E) 9.5 to induce fetal CDH. Sildenafil and/or rosiglitazone were administered to each fetus via an intra-amniotic injection after laparotomy on the pregnant dam at E19.5, and fetuses delivered at E21.5. Efficacy measures were gross necropsy, histology, peripheral blood flow assessment using intra-cardiac injection of a vascular tracer after delivery, and protein expression analysis. Intra-amniotic injections did not affect fetal survival, the incidence of CDH, or lung weight-to-body weight ratio in CDH fetuses. IA sildenafil injection decreased pulmonary vascular muscularization, and rosiglitazone produced an increase in peripheral pulmonary blood flow distribution. The combination of sildenafil and rosiglitazone decreased pulmonary artery smooth muscle cell proliferation. These intra-amniotic treatments did not show any negative effects in either CDH fetuses or control fetuses. IA injection of sildenafil and rosiglitazone late in gestation ameliorates the pulmonary hypertensive phenotype of CDH and may have utility in clinical translation. Not applicable. •What is currently known about this topic? Early gestation intra-amniotic sildenafil administration improves pulmonary hypertension and survival in the nitrogen mouse model of congenital diaphragmatic hernia (CDH). Transplacental (pregnant dam) administration of sildenafil or rosiglitazone has been shown to improve the pulmonary hypertensive phenotype in CDH when initiated as late as E18 in the nitrogen rat model of CDH.•What new information is contained in this article? Intra-amniotic injection of sildenafil and rosiglitazone performed late in gestation (E19.5) is still effective in improving the pulmonary hypertension phenotype of CDH. Sildenafil and rosiglitazone, delivered together by IA injection, reduce pulmonary vascular smooth muscle cell proliferation.
doi_str_mv 10.1016/j.jpedsurg.2024.01.010
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Prenatal therapy may ameliorate postnatal pulmonary hypertension. We hypothesized that intra-amniotic (IA) injection of either sildenafil, a phosphodiesterase 5 inhibitor, or rosiglitazone, a PPAR-γ agonist, or both late in gestation would decrease the detrimental pulmonary vascular remodeling seen in CDH and improve peripheral pulmonary blood flow. Pregnant rats were gavaged with nitrogen on embryonic day (E) 9.5 to induce fetal CDH. Sildenafil and/or rosiglitazone were administered to each fetus via an intra-amniotic injection after laparotomy on the pregnant dam at E19.5, and fetuses delivered at E21.5. Efficacy measures were gross necropsy, histology, peripheral blood flow assessment using intra-cardiac injection of a vascular tracer after delivery, and protein expression analysis. Intra-amniotic injections did not affect fetal survival, the incidence of CDH, or lung weight-to-body weight ratio in CDH fetuses. IA sildenafil injection decreased pulmonary vascular muscularization, and rosiglitazone produced an increase in peripheral pulmonary blood flow distribution. The combination of sildenafil and rosiglitazone decreased pulmonary artery smooth muscle cell proliferation. These intra-amniotic treatments did not show any negative effects in either CDH fetuses or control fetuses. IA injection of sildenafil and rosiglitazone late in gestation ameliorates the pulmonary hypertensive phenotype of CDH and may have utility in clinical translation. Not applicable. •What is currently known about this topic? Early gestation intra-amniotic sildenafil administration improves pulmonary hypertension and survival in the nitrogen mouse model of congenital diaphragmatic hernia (CDH). Transplacental (pregnant dam) administration of sildenafil or rosiglitazone has been shown to improve the pulmonary hypertensive phenotype in CDH when initiated as late as E18 in the nitrogen rat model of CDH.•What new information is contained in this article? Intra-amniotic injection of sildenafil and rosiglitazone performed late in gestation (E19.5) is still effective in improving the pulmonary hypertension phenotype of CDH. 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Prenatal therapy may ameliorate postnatal pulmonary hypertension. We hypothesized that intra-amniotic (IA) injection of either sildenafil, a phosphodiesterase 5 inhibitor, or rosiglitazone, a PPAR-γ agonist, or both late in gestation would decrease the detrimental pulmonary vascular remodeling seen in CDH and improve peripheral pulmonary blood flow. Pregnant rats were gavaged with nitrogen on embryonic day (E) 9.5 to induce fetal CDH. Sildenafil and/or rosiglitazone were administered to each fetus via an intra-amniotic injection after laparotomy on the pregnant dam at E19.5, and fetuses delivered at E21.5. Efficacy measures were gross necropsy, histology, peripheral blood flow assessment using intra-cardiac injection of a vascular tracer after delivery, and protein expression analysis. Intra-amniotic injections did not affect fetal survival, the incidence of CDH, or lung weight-to-body weight ratio in CDH fetuses. IA sildenafil injection decreased pulmonary vascular muscularization, and rosiglitazone produced an increase in peripheral pulmonary blood flow distribution. The combination of sildenafil and rosiglitazone decreased pulmonary artery smooth muscle cell proliferation. These intra-amniotic treatments did not show any negative effects in either CDH fetuses or control fetuses. IA injection of sildenafil and rosiglitazone late in gestation ameliorates the pulmonary hypertensive phenotype of CDH and may have utility in clinical translation. Not applicable. •What is currently known about this topic? Early gestation intra-amniotic sildenafil administration improves pulmonary hypertension and survival in the nitrogen mouse model of congenital diaphragmatic hernia (CDH). Transplacental (pregnant dam) administration of sildenafil or rosiglitazone has been shown to improve the pulmonary hypertensive phenotype in CDH when initiated as late as E18 in the nitrogen rat model of CDH.•What new information is contained in this article? Intra-amniotic injection of sildenafil and rosiglitazone performed late in gestation (E19.5) is still effective in improving the pulmonary hypertension phenotype of CDH. 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Prenatal therapy may ameliorate postnatal pulmonary hypertension. We hypothesized that intra-amniotic (IA) injection of either sildenafil, a phosphodiesterase 5 inhibitor, or rosiglitazone, a PPAR-γ agonist, or both late in gestation would decrease the detrimental pulmonary vascular remodeling seen in CDH and improve peripheral pulmonary blood flow. Pregnant rats were gavaged with nitrogen on embryonic day (E) 9.5 to induce fetal CDH. Sildenafil and/or rosiglitazone were administered to each fetus via an intra-amniotic injection after laparotomy on the pregnant dam at E19.5, and fetuses delivered at E21.5. Efficacy measures were gross necropsy, histology, peripheral blood flow assessment using intra-cardiac injection of a vascular tracer after delivery, and protein expression analysis. Intra-amniotic injections did not affect fetal survival, the incidence of CDH, or lung weight-to-body weight ratio in CDH fetuses. IA sildenafil injection decreased pulmonary vascular muscularization, and rosiglitazone produced an increase in peripheral pulmonary blood flow distribution. The combination of sildenafil and rosiglitazone decreased pulmonary artery smooth muscle cell proliferation. These intra-amniotic treatments did not show any negative effects in either CDH fetuses or control fetuses. IA injection of sildenafil and rosiglitazone late in gestation ameliorates the pulmonary hypertensive phenotype of CDH and may have utility in clinical translation. Not applicable. •What is currently known about this topic? Early gestation intra-amniotic sildenafil administration improves pulmonary hypertension and survival in the nitrogen mouse model of congenital diaphragmatic hernia (CDH). Transplacental (pregnant dam) administration of sildenafil or rosiglitazone has been shown to improve the pulmonary hypertensive phenotype in CDH when initiated as late as E18 in the nitrogen rat model of CDH.•What new information is contained in this article? Intra-amniotic injection of sildenafil and rosiglitazone performed late in gestation (E19.5) is still effective in improving the pulmonary hypertension phenotype of CDH. Sildenafil and rosiglitazone, delivered together by IA injection, reduce pulmonary vascular smooth muscle cell proliferation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38350773</pmid><doi>10.1016/j.jpedsurg.2024.01.010</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-1453-8827</orcidid></addata></record>
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subjects Congenital diaphragmatic hernia
Nitrogen model
Pulmonary hypertension
Rosiglitazone
Sildenafil
title Intra-Amniotic Sildenafil and Rosiglitazone Late in Gestation Ameliorate the Pulmonary Hypertension Phenotype in Congenital Diaphragmatic Hernia
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