Prophylactic Intra-Uterine β-Cyclodextrin Administration during Intra-Uterine Ureaplasma parvum Infection Partly Prevents Liver Inflammation without Interfering with the Enterohepatic Circulation of the Fetal Sheep
Chorioamnionitis can lead to inflammation and injury of the liver and gut, thereby predisposing patients to adverse outcomes such as necrotizing enterocolitis (NEC). In addition, intestinal bile acids (BAs) accumulation is causally linked to NEC development. Plant sterols are a promising interventio...
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Published in | Nutrients Vol. 12; no. 5; p. 1312 |
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Abstract | Chorioamnionitis can lead to inflammation and injury of the liver and gut, thereby predisposing patients to adverse outcomes such as necrotizing enterocolitis (NEC). In addition, intestinal bile acids (BAs) accumulation is causally linked to NEC development. Plant sterols are a promising intervention to prevent NEC development, considering their anti-inflammatory properties in the liver. Therefore, we investigated whether an intra-amniotic (IA)
(UP) infection affected the liver and enterohepatic circulation (EHC) and evaluated whether an IA administered plant sterol mixture dissolved in β-cyclodextrin exerted prophylactic effects. An ovine chorioamnionitis model was used in which liver inflammation and the EHC were assessed following IA UP exposure in the presence or absence of IA prophylactic plant sterols (a mixture of β-sitosterol and campesterol dissolved in β-cyclodextrin (carrier)) or carrier alone. IA UP exposure caused an inflammatory reaction in the liver, histologically seen as clustered and conflated hepatic erythropoiesis in the parenchyma, which was partially prevented by IA administration of sterol + β-cyclodextrin, or β-cyclodextrin alone. In addition, IA administration of β-cyclodextrin prior to UP caused changes in the expression of several hepatic BAs transporters, without causing alterations in other aspects of the EHC. Thereby, the addition of plant sterols to the carrier β-cyclodextrin did not have additional effects. |
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AbstractList | Chorioamnionitis can lead to inflammation and injury of the liver and gut, thereby predisposing patients to adverse outcomes such as necrotizing enterocolitis (NEC). In addition, intestinal bile acids (BAs) accumulation is causally linked to NEC development. Plant sterols are a promising intervention to prevent NEC development, considering their anti-inflammatory properties in the liver. Therefore, we investigated whether an intra-amniotic (IA)
(UP) infection affected the liver and enterohepatic circulation (EHC) and evaluated whether an IA administered plant sterol mixture dissolved in β-cyclodextrin exerted prophylactic effects. An ovine chorioamnionitis model was used in which liver inflammation and the EHC were assessed following IA UP exposure in the presence or absence of IA prophylactic plant sterols (a mixture of β-sitosterol and campesterol dissolved in β-cyclodextrin (carrier)) or carrier alone. IA UP exposure caused an inflammatory reaction in the liver, histologically seen as clustered and conflated hepatic erythropoiesis in the parenchyma, which was partially prevented by IA administration of sterol + β-cyclodextrin, or β-cyclodextrin alone. In addition, IA administration of β-cyclodextrin prior to UP caused changes in the expression of several hepatic BAs transporters, without causing alterations in other aspects of the EHC. Thereby, the addition of plant sterols to the carrier β-cyclodextrin did not have additional effects. Chorioamnionitis can lead to inflammation and injury of the liver and gut, thereby predisposing patients to adverse outcomes such as necrotizing enterocolitis (NEC). In addition, intestinal bile acids (BAs) accumulation is causally linked to NEC development. Plant sterols are a promising intervention to prevent NEC development, considering their anti-inflammatory properties in the liver. Therefore, we investigated whether an intra-amniotic (IA) Ureaplasma parvum (UP) infection affected the liver and enterohepatic circulation (EHC) and evaluated whether an IA administered plant sterol mixture dissolved in β-cyclodextrin exerted prophylactic effects. An ovine chorioamnionitis model was used in which liver inflammation and the EHC were assessed following IA UP exposure in the presence or absence of IA prophylactic plant sterols (a mixture of β-sitosterol and campesterol dissolved in β-cyclodextrin (carrier)) or carrier alone. IA UP exposure caused an inflammatory reaction in the liver, histologically seen as clustered and conflated hepatic erythropoiesis in the parenchyma, which was partially prevented by IA administration of sterol + β-cyclodextrin, or β-cyclodextrin alone. In addition, IA administration of β-cyclodextrin prior to UP caused changes in the expression of several hepatic BAs transporters, without causing alterations in other aspects of the EHC. Thereby, the addition of plant sterols to the carrier β-cyclodextrin did not have additional effects. Chorioamnionitis can lead to inflammation and injury of the liver and gut, thereby predisposing patients to adverse outcomes such as necrotizing enterocolitis (NEC). In addition, intestinal bile acids (BAs) accumulation is causally linked to NEC development. Plant sterols are a promising intervention to prevent NEC development, considering their anti-inflammatory properties in the liver. Therefore, we investigated whether an intra-amniotic (IA) Ureaplasma parvum (UP) infection affected the liver and enterohepatic circulation (EHC) and evaluated whether an IA administered plant sterol mixture dissolved in β-cyclodextrin exerted prophylactic effects. An ovine chorioamnionitis model was used in which liver inflammation and the EHC were assessed following IA UP exposure in the presence or absence of IA prophylactic plant sterols (a mixture of β-sitosterol and campesterol dissolved in β-cyclodextrin (carrier)) or carrier alone. IA UP exposure caused an inflammatory reaction in the liver, histologically seen as clustered and conflated hepatic erythropoiesis in the parenchyma, which was partially prevented by IA administration of sterol + β-cyclodextrin, or β-cyclodextrin alone. In addition, IA administration of β-cyclodextrin prior to UP caused changes in the expression of several hepatic BAs transporters, without causing alterations in other aspects of the EHC. Thereby, the addition of plant sterols to the carrier β-cyclodextrin did not have additional effects. |
Author | Payne, Matthew S Heymans, Cathelijne Lenaerts, Kaatje Spiller, Owen B Beeton, Michael L Plat, Jogchum Hadfoune, Mhamed Kemp, Matthew W den Dulk, Marcel Stock, Sarah J Heij, Lara R Wolfs, Tim G A M Jobe, Alan H van Gemert, Wim G van Heugten, Chantal Kramer, Boris W |
AuthorAffiliation | 8 Division of Obstetrics and Gynecology, The University of Western Australia, Crawley WA 6009, Australia; alan.jobe@cchmc.org (A.H.J.); matthew.payne@uwa.edu.au (M.S.P.); matthew.kemp@uwa.edu.au (M.W.K.) 12 Neonatology, Department of Pediatrics, Maastricht University Medical Center, 6202 AZ Maastricht, The Netherlands 3 Department of Pathology, University Hospital Aachen, 52074 Aachen, Germany 6 Cardiff School of Sport and Health Sciences, Cardiff Metropolitan University, Cardiff CF5 2YB, UK; mbeeton@cardiffmet.ac.uk 4 Department of Surgery, Maastricht University Medical Center, 6202 AZ Maastricht, The Netherlands 10 School of Veterinary and Life Sciences, Murdoch University, Perth WA 6150, Australia 14 Department of Biomedical Engineering (BMT), School for Cardiovascular Diseases (CARIM), Maastricht University, 6200 MD Maastricht, The Netherlands 13 Department of Nutrition and Movement Sciences, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 |
AuthorAffiliation_xml | – name: 8 Division of Obstetrics and Gynecology, The University of Western Australia, Crawley WA 6009, Australia; alan.jobe@cchmc.org (A.H.J.); matthew.payne@uwa.edu.au (M.S.P.); matthew.kemp@uwa.edu.au (M.W.K.) – name: 10 School of Veterinary and Life Sciences, Murdoch University, Perth WA 6150, Australia – name: 13 Department of Nutrition and Movement Sciences, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands; j.plat@maastrichtuniversity.nl – name: 6 Cardiff School of Sport and Health Sciences, Cardiff Metropolitan University, Cardiff CF5 2YB, UK; mbeeton@cardiffmet.ac.uk – name: 2 Department of Surgery, University Hospital Aachen, 52074 Aachen, Germany; marcel.den.dulk@mumc.nl – name: 7 Usher Institute, University of Edinburgh, Edinburgh EH16 4TJ, UK; sarah.stock@ed.ac.uk – name: 5 Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff CF10 3AT, UK; spillerb@cardiff.ac.uk – name: 11 Department of Pediatrics, School for Oncology and Developmental Biology (GROW), Maastricht University, 6200 MD Maastricht, The Netherlands; b.kramer@maastrichtuniversity.nl – name: 9 Division of Neonatology/Pulmonary Biology, The Perinatal Institute, Cincinnati Children’s Hospital Medical Center, University of Cincinnati, Cincinnati, OH 45229, USA – name: 3 Department of Pathology, University Hospital Aachen, 52074 Aachen, Germany – name: 12 Neonatology, Department of Pediatrics, Maastricht University Medical Center, 6202 AZ Maastricht, The Netherlands – name: 14 Department of Biomedical Engineering (BMT), School for Cardiovascular Diseases (CARIM), Maastricht University, 6200 MD Maastricht, The Netherlands – name: 4 Department of Surgery, Maastricht University Medical Center, 6202 AZ Maastricht, The Netherlands – name: 1 Department of Surgery, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands; c.heymans@maastrichtuniversity.nl (C.H.); l.heij@maastrichtuniversity.nl (L.R.H.); kaatje.lenaerts@maastrichtuniversity.nl (K.L.); m.hadfoune@maastrichtuniversity.nl (M.H.); chantalvanheugten@hotmail.com (C.v.H.); wim.van.gemert@mumc.nl (W.G.v.G.) |
Author_xml | – sequence: 1 givenname: Cathelijne orcidid: 0000-0001-9373-1360 surname: Heymans fullname: Heymans, Cathelijne organization: Department of Surgery, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands – sequence: 2 givenname: Lara R orcidid: 0000-0002-0602-3356 surname: Heij fullname: Heij, Lara R organization: Department of Pathology, University Hospital Aachen, 52074 Aachen, Germany – sequence: 3 givenname: Kaatje surname: Lenaerts fullname: Lenaerts, Kaatje organization: Department of Surgery, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands – sequence: 4 givenname: Marcel surname: den Dulk fullname: den Dulk, Marcel organization: Department of Surgery, Maastricht University Medical Center, 6202 AZ Maastricht, The Netherlands – sequence: 5 givenname: Mhamed surname: Hadfoune fullname: Hadfoune, Mhamed organization: Department of Surgery, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands – sequence: 6 givenname: Chantal surname: van Heugten fullname: van Heugten, Chantal organization: Department of Surgery, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands – sequence: 7 givenname: Owen B orcidid: 0000-0002-9117-6911 surname: Spiller fullname: Spiller, Owen B organization: Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff CF10 3AT, UK – sequence: 8 givenname: Michael L surname: Beeton fullname: Beeton, Michael L organization: Cardiff School of Sport and Health Sciences, Cardiff Metropolitan University, Cardiff CF5 2YB, UK – sequence: 9 givenname: Sarah J surname: Stock fullname: Stock, Sarah J organization: Usher Institute, University of Edinburgh, Edinburgh EH16 4TJ, UK – sequence: 10 givenname: Alan H surname: Jobe fullname: Jobe, Alan H organization: Division of Neonatology/Pulmonary Biology, The Perinatal Institute, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH 45229, USA – sequence: 11 givenname: Matthew S surname: Payne fullname: Payne, Matthew S organization: Division of Obstetrics and Gynecology, The University of Western Australia, Crawley WA 6009, Australia – sequence: 12 givenname: Matthew W surname: Kemp fullname: Kemp, Matthew W organization: School of Veterinary and Life Sciences, Murdoch University, Perth WA 6150, Australia – sequence: 13 givenname: Boris W surname: Kramer fullname: Kramer, Boris W organization: Neonatology, Department of Pediatrics, Maastricht University Medical Center, 6202 AZ Maastricht, The Netherlands – sequence: 14 givenname: Jogchum surname: Plat fullname: Plat, Jogchum organization: Department of Nutrition and Movement Sciences, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD Maastricht, The Netherlands – sequence: 15 givenname: Wim G surname: van Gemert fullname: van Gemert, Wim G organization: Department of Surgery, Maastricht University Medical Center, 6202 AZ Maastricht, The Netherlands – sequence: 16 givenname: Tim G A M orcidid: 0000-0003-4417-4144 surname: Wolfs fullname: Wolfs, Tim G A M organization: Department of Biomedical Engineering (BMT), School for Cardiovascular Diseases (CARIM), Maastricht University, 6200 MD Maastricht, The Netherlands |
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CitedBy_id | crossref_primary_10_1016_j_biopha_2023_115243 crossref_primary_10_1155_2022_5784146 crossref_primary_10_3390_metabo13070836 crossref_primary_10_1038_s41598_021_89542_4 |
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Keywords | preterm birth Ureaplasma parvum liver plant sterols intra-uterine infection chorioamnionitis sheep enterohepatic circulation |
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SubjectTerms | Acids Animals Anti-inflammatory agents beta-Cyclodextrins Bile Bile acids Cesarean section Cholesterol - administration & dosage Cholesterol - analogs & derivatives Cholesterol - pharmacology Chorioamnionitis Chorioamnionitis - drug therapy Chorioamnionitis - microbiology Cyclodextrins Disease Models, Animal Drug Carriers Enterocolitis Enterocolitis, Necrotizing - microbiology Enterocolitis, Necrotizing - prevention & control Enterohepatic Circulation - drug effects Erythropoiesis Exposure Female Fetus - blood supply Fetuses Gene expression Histology Infections Inflammation Injections, Intralesional Intestine intra-uterine infection Liver Liver - blood supply Necrotizing enterocolitis Newborn babies Parenchyma Phytosterols - administration & dosage Phytosterols - pharmacology Phytotherapy plant sterols Post-Exposure Prophylaxis - methods Pregnancy Premature birth preterm birth Proteins Sheep Sitosterols - administration & dosage Sitosterols - pharmacology Software Sterols Ureaplasma Ureaplasma Infections Ureaplasma parvum Uterus Veins & arteries β-Cyclodextrin |
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Title | Prophylactic Intra-Uterine β-Cyclodextrin Administration during Intra-Uterine Ureaplasma parvum Infection Partly Prevents Liver Inflammation without Interfering with the Enterohepatic Circulation of the Fetal Sheep |
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