Dietary Carbohydrates and Fat Induce Distinct Surfactant Alterations in Mice.


Journal

American journal of respiratory cell and molecular biology
ISSN: 1535-4989
Titre abrégé: Am J Respir Cell Mol Biol
Pays: United States
ID NLM: 8917225

Informations de publication

Date de publication:
03 2021
Historique:
pubmed: 23 12 2020
medline: 26 3 2021
entrez: 22 12 2020
Statut: ppublish

Résumé

Obesity and type 2 diabetes are nutrition-related conditions associated with lung function impairment and pulmonary diseases; however, the underlying pathomechanisms are incompletely understood. Pulmonary surfactant is essential for lung function, and surfactant synthesis by AT2 (alveolar epithelial type 2) cells relies on nutrient uptake. We hypothesized that dietary amounts of carbohydrates or fat affect surfactant homeostasis and composition. Feeding mice a starch-rich diet (StD), sucrose-rich diet (SuD), or fat-rich diet (FaD) for 30 weeks resulted in hypercholesterolemia and hyperinsulinemia compared with a fiber-rich control diet. In SuD and FaD groups, lung mechanic measurements revealed viscoelastic changes during inspiration, indicating surfactant alterations, and interfacial adsorption of isolated surfactant at the air-liquid interface was decreased under FaD. The composition of characteristic phospholipid species was modified, including a shift from dipalmitoyl-phosphatidylcholine (PC16:0/16:0) to palmitoyl-palmitoleoyl-phosphatidylcholine (PC16:0/16:1) in response to carbohydrates and decreased myristic acid-containing phosphatidylcholine species (PC14:0/14:0; PC16:0/14:0) on excess fat intake, as well as higher palmitoyl-oleoyl-phosphatidylglycerol (PG16:0/18:1) and palmitoyl-linoleoyl-phosphatidylglycerol (PG16:0/18:2) fractions in StD, SuD, and FaD groups than in the control diet. Moreover, mRNA expression levels of surfactant synthesis-related proteins within AT2 cells were altered. Under the StD regimen, AT2 cells showed prominent lipid accumulations and smaller lamellar bodies. Thus, in an established mouse model, distinct diet-related surfactant alterations were subtle, yet detectable, and may become challenging under conditions of reduced respiratory capacity. Dietary fat was the only macronutrient significantly affecting surfactant function. This warrants future studies examining alimentary effects on lung surfactant, with special regard to pulmonary complications in obesity and type 2 diabetes.

Identifiants

pubmed: 33351709
doi: 10.1165/rcmb.2020-0335OC
doi:

Substances chimiques

Dietary Carbohydrates 0
Dietary Fats 0
Phospholipids 0
Pulmonary Surfactants 0
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

379-390

Commentaires et corrections

Type : CommentIn

Auteurs

Julia Schipke (J)

Institute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
Biomedical Research in Endstage and Obstructive Lung Disease-Hannover, German Center for Lung Research, Hannover, Germany.
Cluster of Excellence Regenerative Biology to Reconstructive Therapy, Hannover, Germany.

Dagmar Jütte (D)

Institute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.

Christina Brandenberger (C)

Institute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
Biomedical Research in Endstage and Obstructive Lung Disease-Hannover, German Center for Lung Research, Hannover, Germany.
Cluster of Excellence Regenerative Biology to Reconstructive Therapy, Hannover, Germany.

Chiara Autilio (C)

Department of Biochemistry and Molecular Biology, Biology and Research Institute-Hospital, Complutense University, Madrid, Spain.

Jesus Perez-Gil (J)

Department of Biochemistry and Molecular Biology, Biology and Research Institute-Hospital, Complutense University, Madrid, Spain.

Wolfgang Bernhard (W)

Department of Neonatology, Eberhard-Karls University, Tübingen, Germany.

Matthias Ochs (M)

Institute of Functional Anatomy, Charité University of Medicine-Berlin, Berlin, Germany; and.
German Center for Lung Research, Berlin, Germany.

Christian Mühlfeld (C)

Institute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
Biomedical Research in Endstage and Obstructive Lung Disease-Hannover, German Center for Lung Research, Hannover, Germany.
Cluster of Excellence Regenerative Biology to Reconstructive Therapy, Hannover, Germany.

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Classifications MeSH