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1.
Ophthalmologica ; 246(3-4): 169-173, 2023.
Article in English | MEDLINE | ID: mdl-37579736

ABSTRACT

Germany's health care footprint accounts for 5.2% of the national emissions footprint which results in 0.71 tons of CO2 emission per capita. Thus, the health sector has a responsibility to take climate action. Surgery is a resource-intensive health care activity, requiring expensive equipment, sterilization procedures, advanced operative technologies, and obligatory life support systems. We spotlight the situation in a department of ophthalmology with frequent anesthesia services and highly standardized procedures. This narrative review discusses high-impact actions which result in a major reduction of the CO2 footprint according to the global road map for health care decarbonization, considering both the ophthalmic and anesthesiologic point of view.


Subject(s)
Carbon Dioxide , Ophthalmology , Humans , Carbon Footprint , Ophthalmologic Surgical Procedures , Eye
2.
Mediators Inflamm ; 2020: 8294342, 2020.
Article in English | MEDLINE | ID: mdl-32617075

ABSTRACT

Sepsis is associated with a strong inflammatory reaction triggering a complex and prolonged immune response. Septic patients have been shown to develop sustained immunosuppression due to a reduced responsiveness of leukocytes to pathogens. Changes in cellular metabolism of leukocytes have been linked to this phenomenon and contribute to the ongoing immunological derangement. However, the underlying mechanisms of these phenomena are incompletely understood. In cell culture models, we mimicked LPS tolerance conditions to provide evidence that epigenetic modifications account for monocyte metabolic changes which cause immune paralysis in restimulated septic monocytes. In detail, we observed differential methylation of CpG sites related to metabolic activity in human PBMCs 18 h after septic challenge. The examination of changes in immune function and metabolic pathways was performed in LPS-tolerized monocytic THP-1 cells. Passaged THP-1 cells, inheriting initial LPS challenge, presented with dysregulation of cytokine expression and oxygen consumption for up to 7 days after the initial LPS treatment. Proinflammatory cytokine concentrations of TNFα and IL1ß were significantly suppressed following a second LPS challenge (p < 0.001) on day 7 after first LPS stimulation. However, the analysis of cellular metabolism did not reveal any noteworthy alterations between tolerant and nontolerant THP-1 monocytes. No quantitative differences in ATP and NADH synthesis or participating enzymes of energy metabolism occurred. Our data demonstrate that the function and epigenetic modifications of septic and tolerized monocytes can be examined in vitro with the help of our LPS model. Changes in CpG site methylation and monocyte function point to a correlation between epigenetic modification in metabolic pathways and reduced monocyte function under postseptic conditions.


Subject(s)
Endotoxins/pharmacology , Leukocytes, Mononuclear/drug effects , Leukocytes, Mononuclear/metabolism , Adenosine Triphosphate/metabolism , Cell Line , Cells, Cultured , Enzyme-Linked Immunosorbent Assay , Healthy Volunteers , Humans , Lactic Acid/metabolism , Lipopolysaccharides/pharmacology , NAD/metabolism , Real-Time Polymerase Chain Reaction , THP-1 Cells
3.
Anaesthesiologie ; 73(3): 168-176, 2024 03.
Article in German | MEDLINE | ID: mdl-38334810

ABSTRACT

Aortic valve stenosis is a common condition that requires an anesthesiologist's in-depth knowledge of the pathophysiology, diagnostics and perioperative features of the disease. A newly diagnosed aortic valve stenosis is often initially identified from the anamnesis (dyspnea, syncope, angina pectoris) or a suspicious auscultation finding during the anesthesiologist's preoperative assessment. Interdisciplinary collaboration is essential to ensure the optimal management of these patients in the perioperative setting. An accurate anamnesis and examination during the preoperative assessment are crucial to select the most suitable anesthetic approach. Additionally, a precise understanding of the hemodynamic peculiarities associated with aortic valve stenosis is necessary. After a short summary of the overall pathophysiology of aortic valve stenosis, this review article focuses on the specific anesthetic considerations, risk factors for complications, and the perioperative management for noncardiac surgery in patients with aortic valve stenosis.


Subject(s)
Anesthesia , Anesthetics , Aortic Valve Stenosis , Humans , Aortic Valve Stenosis/complications , Risk Factors , Syncope/complications
4.
J Vis Exp ; (149)2019 07 06.
Article in English | MEDLINE | ID: mdl-31329180

ABSTRACT

Airway administration of lipopolysaccharide (LPS) is a common way to study pulmonary inflammation and acute lung injury (ALI) in small animal models. Various approaches have been described, such as the inhalation of aerosolized LPS as well as nasal or intratracheal instillation. The presented protocol describes a detailed step-by-step procedure to induce ALI in mice by direct intratracheal LPS instillation and perform FACS analysis of blood samples, bronchoalveolar lavage (BAL) fluid, and lung tissue. After intraperitoneal sedation, the trachea is exposed and LPS is administered via a 22 G venous catheter. A robust and reproducible inflammatory reaction with leukocyte invasion, upregulation of proinflammatory cytokines, and disruption of the alveolo-capillary barrier is induced within hours to days, depending on the LPS dosage used. Collection of blood samples, BAL fluid, and lung harvesting, as well as the processing for FACS analysis, are described in detail in the protocol. Although the use of the sterile LPS is not suitable to study pharmacologic interventions in infectious diseases, the described approach offers minimal invasiveness, simple handling, and good reproducibility to answer mechanistic immunological questions. Furthermore, dose titration as well as the use of alternative LPS preparations or mouse strains allow modulation of the clinical effects, which can exhibit different degrees of ALI severity or early vs. late onset of disease symptoms.


Subject(s)
Acute Lung Injury/chemically induced , Lipopolysaccharides/administration & dosage , Lipopolysaccharides/toxicity , Acute Lung Injury/immunology , Acute Lung Injury/pathology , Animals , Chemotaxis, Leukocyte/drug effects , Cytokines/metabolism , Disease Models, Animal , Female , Inflammation , Instillation, Drug , Intubation, Intratracheal , Lung/drug effects , Lung/immunology , Lung/pathology , Mice , Reproducibility of Results
5.
Clin J Am Soc Nephrol ; 10(10): 1841-51, 2015 Oct 07.
Article in English | MEDLINE | ID: mdl-25568218

ABSTRACT

The mononuclear phagocytes (dendritic cells and macrophages) are closely related immune cells with central roles in anti-infectious defense and maintenance of organ integrity. The canonical function of dendritic cells is the activation of T cells, whereas macrophages remove apoptotic cells and microbes by phagocytosis. In the kidney, these cell types form an intricate system of mononuclear phagocytes that surveys against injury and infection and contributes to organ homeostasis and tissue repair but may also promote progression of CKD. This review summarizes the general functions and classification of dendritic cells and macrophages in the immune system and recapitulates why overlapping definitions and historically separate research have created controversy about their tasks. Their roles in acute kidney disease, CKD, and renal transplantation are described, and therapeutic strategy to modify these cells for therapeutic purposes is discussed.


Subject(s)
Dendritic Cells/immunology , Kidney Diseases/immunology , Kidney/cytology , Kidney/immunology , Macrophages/immunology , Urinary Tract Infections/immunology , Animals , Dendritic Cells/physiology , Humans , Immune Tolerance , Immunotherapy , Kidney Transplantation , Macrophages/physiology , Phenotype , Receptors, Pattern Recognition
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