Effect of Supernatant from Fibroblasts from the Progeny of Female Rats with Chronic Liver Disease of Different Origin on the Morphology and Function of Cultured Peritoneal Macrophages

2013 ◽  
Vol 154 (4) ◽  
pp. 512-514
Author(s):  
G. V. Bryukhin ◽  
I. V. Zubarev
PLoS ONE ◽  
2013 ◽  
Vol 8 (12) ◽  
pp. e80703 ◽  
Author(s):  
Barbara Czech ◽  
Katja Dettmer ◽  
Daniela Valletta ◽  
Michael Saugspier ◽  
Andreas Koch ◽  
...  

Author(s):  
Ricky Sinharay

Gastroenterology and hepatology encompass a vast array of organs that have diverse structure and function and are affected by a multitude of disease processes. Diseases of the digestive tract are a major cause of morbidity and mortality in the United Kingdom (UK) and worldwide. There have been great advances in our understanding, diagnosis, and management of gastrointestinal (GI) disease, and knowledge continues to develop at a great pace. Understanding the physiology and cellular and molecular events that drive pathological processes, as well as the devel­opment of sophisticated endoscopic and radiological tests, have trans­formed diagnostic capability. Therapeutic endoscopy has progressed to replace surgical management of common GI emergencies such as upper GI tract bleeding and decompressing biliary tract obstruction. However, as ever, there is still much work to be done. For example, the advances in biologic immunotherapy in inflammatory bowel disease has greatly im­proved patients’ quality of life and a reduction in the need for surgery, though the overall impact of these medications on the natural history of the disease is debatable at present. Hepatology is a greatly misunderstood specialty. The physiological changes that occur as cirrhosis and portal hypertension develop are the key to understanding all manifestations of a decompensating liver. Recently, there has been a significant increase in the prevalence of chronic liver disease in the UK, and as a result, hospital admissions have increased. Liver disease is the only major cause of death still increasing year on year, and twice as many people now die from liver disease than in 1991. The 2013 National Confidential Enquiry into Patient Outcome and Death (NCEPOD) of patients with alcohol- related liver disease (ARLD) found that less than half the number of patients who died from ARLD received ‘good care’, and avoidable deaths were identified. Allied to this, the enquiry shed light on a cultural pessimism regarding outcomes and prognosis of chronic liver disease and, in particular, ARLD from both the public and the medical profession as a whole. There is now a concerted drive towards improving awareness of chronic liver disease, and initial simple supportive treatments can greatly improve sur­vival, more so than previously thought.


2008 ◽  
Vol 27 (11) ◽  
pp. 1017-1029 ◽  
Author(s):  
P. WITTERS ◽  
K. FRESON ◽  
C. VERSLYPE ◽  
K. PEERLINCK ◽  
M. HOYLAERTS ◽  
...  

2021 ◽  
Vol 22 (15) ◽  
pp. 8309
Author(s):  
Sung-Min Won ◽  
Eunju Park ◽  
Jin-Ju Jung ◽  
Raja Ganesan ◽  
Haripriya Gupta ◽  
...  

In chronic liver disease, the causative factor is important; however, recently, the intestinal microbiome has been associated with the progression of chronic liver disease and the occurrence of side effects. The immune system is affected by the metabolites of the microbiome, and diet is the primary regulator of the microbiota composition and function in the gut–liver axis. These metabolites can be used as therapeutic material, and postbiotics, in the future, can increase or decrease human immunity by modulating inflammation and immune reactions. Therefore, the excessive intake of nutrients and the lack of nutrition have important effects on immunity and inflammation. Evidence has been published indicating that microbiome-induced chronic inflammation and the consequent immune dysregulation affect the development of chronic liver disease. In this research paper, we discuss the overall trend of microbiome-derived substances related to immunity and the future research directions.


2011 ◽  
Vol 49 (01) ◽  
Author(s):  
B Czech ◽  
A Stevens ◽  
G Kirovski ◽  
M Saugspier ◽  
C Dorn ◽  
...  

2012 ◽  
Vol 426 (3) ◽  
pp. 404-408 ◽  
Author(s):  
Daniela Valletta ◽  
Barbara Czech ◽  
Wolfgang E. Thasler ◽  
Martina Müller ◽  
Anja-Katrin Bosserhoff ◽  
...  

Life ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 899
Author(s):  
Chisato Saeki ◽  
Akihito Tsubota

The liver plays a pivotal role in nutrient/energy metabolism and storage, anabolic hormone regulation, ammonia detoxification, and cytokine production. Impaired liver function can cause malnutrition, hyperammonemia, and chronic inflammation, leading to an imbalance between muscle protein synthesis and proteolysis. Patients with chronic liver disease (CLD) have a high prevalence of sarcopenia, characterized by progressive loss of muscle mass and function, affecting health-related quality of life and prognosis. Recent reports have revealed that osteosarcopenia, defined as the concomitant occurrence of sarcopenia and osteoporosis, is also highly prevalent in patients with CLD. Since the differentiation and growth of muscles and bones are closely interrelated through mechanical and biochemical communication, sarcopenia and osteoporosis often progress concurrently and affect each other. Osteosarcopenia further exacerbates unfavorable health outcomes, such as vertebral fracture and frailty. Therefore, a comprehensive assessment of sarcopenia, osteoporosis, and osteosarcopenia, and an understanding of the pathogenic mechanisms involving the liver, bones, and muscles, are important for prevention and treatment. This review summarizes the molecular mechanisms of sarcopenia and osteosarcopenia elucidated to data in hopes of promoting advances in treating these musculoskeletal disorders in patients with CLD.


PLoS ONE ◽  
2016 ◽  
Vol 11 (6) ◽  
pp. e0157771 ◽  
Author(s):  
Victoria L. Gadd ◽  
Preya J. Patel ◽  
Sara Jose ◽  
Leigh Horsfall ◽  
Elizabeth E. Powell ◽  
...  

2020 ◽  
Vol 40 (04) ◽  
pp. 373-384
Author(s):  
Raquel Maeso-Díaz ◽  
Jordi Gracia-Sancho

AbstractAging increases the incidence of chronic liver disease (CLD), worsens its prognosis, and represents the predominant risk factor for its development at all different stages. The hepatic sinusoid, which is fundamental for maintaining liver homeostasis, is composed by hepatocytes, liver sinusoidal endothelial cells, hepatic stellate cells, and hepatic macrophages. During CLD progression, hepatic cells suffer deregulations in their phenotype, which ultimately lead to disease development. The effects of aging on the hepatic sinusoid phenotype and function are not well understood, nevertheless, studies performed in experimental models of liver diseases and aging demonstrate alterations in all hepatic sinusoidal cells. This review provides an updated description of age-related changes in the hepatic sinusoid and discusses the implications for CLD development and treatment. Lastly, we propose aging as a novel therapeutic target to treat liver diseases and summarize the most promising therapies to prevent or improve CLD and extend healthspan.


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