scholarly journals LPS-binding protein mediates LPS-induced liver injury and mortality in the setting of biliary obstruction

2009 ◽  
Vol 296 (1) ◽  
pp. G45-G54 ◽  
Author(s):  
Rebecca M. Minter ◽  
Xiaoming Bi ◽  
Gal Ben-Josef ◽  
Tianyi Wang ◽  
Bin Hu ◽  
...  

It is generally accepted that low levels of lipopolysaccharide (LPS)-binding protein (LBP) augment the cell's response to LPS, whereas high levels of LBP have been shown to inhibit cell responses to LPS. Clinical studies and in vitro work by our group have demonstrated that, in the setting of liver disease, increased or acute-phase levels of LBP may actually potentiate rather than inhibit an overwhelming proinflammatory response. Therefore, in the present studies we sought to determine the role of acute-phase LBP in mediating morbidity and mortality in animals challenged with LPS in the setting of biliary obstruction. Using LBP-deficient mice and LBP blockade in wild-type mice, we demonstrate that high levels of LBP are deleterious in the setting of cholestasis. Following biliary obstruction and intraperitoneal LPS challenge, hepatic injury, hepatic neutrophil infiltration, and mortality were significantly increased in animals with an intact LBP acute-phase response. Kupffer cell responses from these animals demonstrated a significant increase in several inflammatory mediators, and Kupffer cell-associated LBP appears to be responsible for these differences, at least in part. Our results indicate that the role of LBP signaling in inflammatory conditions is complex and heterogeneous, and elevated levels of LBP are not always protective. Increased LBP production in the setting of cholestatic liver disease appears to be deleterious and may represent a potential therapeutic target for preventing overwhelming inflammatory responses to LPS in this setting.

2001 ◽  
Vol 120 (5) ◽  
pp. A27-A27
Author(s):  
M FAN ◽  
S GOYERT ◽  
A AMINLARI ◽  
R KLEIN ◽  
L STEINSTRAESSER ◽  
...  

Author(s):  
Nehal El Koofy ◽  
Noha Yassin ◽  
Sawsan Okasha ◽  
Hany William ◽  
Wafaa Elakel ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A27
Author(s):  
Ming Hui Fan ◽  
Sanna M. Goyert ◽  
Alireza Aminlari ◽  
Richard D. Klein ◽  
Lars Steinstraesser ◽  
...  

Critical Care ◽  
2014 ◽  
Vol 18 (5) ◽  
Author(s):  
Giuseppe Castellano ◽  
Alessandra Stasi ◽  
Angelica Intini ◽  
Margherita Gigante ◽  
Anna Maria Di Palma ◽  
...  

2020 ◽  
Vol 40 (04) ◽  
pp. 403-410
Author(s):  
April O'Brien ◽  
Olga Gasheva ◽  
Gianfranco Alpini ◽  
David Zawieja ◽  
Anatoliy Gashev ◽  
...  

AbstractCholestatic liver disease affects millions of people worldwide and stems from a plethora of causes such as immune dysfunction, genetics, cancerous growths, and lifestyle choices. While not considered a classical lymphatic organ, the liver plays a vital role in the lymph system producing up to half of the body's lymph per day. The lymphatic system is critical to the health of an organism with its networks of vessels that provide drainage for lymphatic fluid and routes for surveilling immune cells. Cholestasis results in an increase of inflammatory cytokines, growth factors, and inflammatory infiltrate. Left unchecked, further disease progression will include collagen deposition which impedes both the hepatic and lymphatic ducts, eventually resulting in an increase in hepatic decompensation, increasing portal pressures, and accumulation of fluid within the abdominal cavity (ascites). Despite the documented interplay between these vital systems, little is known about the effect of liver disease on the lymph system and its biological response. This review looks at the current cholestatic literature from the perspective of the lymphatic system and summarizes what is known about the role of the lymph system in liver pathogenesis during hepatic injury and remodeling, immune-modulating events, or variations in interstitial pressures.


2019 ◽  
Vol 179 (1) ◽  
pp. 10-16 ◽  
Author(s):  
Aziza Saidova ◽  
Merima Bublin ◽  
Klara Schmidthaler ◽  
Veronika Fajgelj ◽  
Florian Klinglmueller ◽  
...  

2018 ◽  
Vol 2 (2) ◽  
pp. 51-56
Author(s):  
Zoya Chaudhry ◽  
Sylviane Forget ◽  
Van-Hung Nguyen ◽  
Najma Ahmed

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
James H. Tabibian ◽  
Jayant A. Talwalkar ◽  
Keith D. Lindor

Primary sclerosing cholangitis (PSC) is an idiopathic, progressive, cholestatic liver disease with considerable morbidity and mortality and no established pharmacotherapy. In addition to the long-recognized association between PSC and inflammatory bowel disease, several lines of preclinical and clinical evidence implicate the microbiota in the etiopathogenesis of PSC. Here we provide a concise review of these data which, taken together, support further investigation of the role of the microbiota and antibiotics in PSC as potential avenues toward elucidating safe and effective pharmacotherapy for patients afflicted by this illness.


2013 ◽  
Vol 18 (3) ◽  
pp. 241-346 ◽  
Author(s):  
Sarah Dillon ◽  
Joseph D. Tobias

Intractable itching is a symptom of cholestatic liver disease of various causes that is bothersome and difficult to manage. Although treatment of the primary cause of cholestasis is paramount in resolving the issue, given the debilitating consequences of pruritus, symptomatic treatment is frequently necessary. Although many medications including cholestyramine, rifampin, opioid antagonists (i.e., naloxone, naltrexone), phenobarbital, and antihistamines have been used to treat cholestatic-induced pruritus, none has resulted in uniform success. We report anecdotal success with the use of ondansetron to treat pruritus associated with cholestasis following prolonged intensive care unit course of a 16-year-old. The theories accounting for pruritus with cholestasis are presented, treatment options are reviewed, and the role of ondansetron in the treatment of pruritus is discussed.


1997 ◽  
Vol 25 (3) ◽  
pp. 301-306 ◽  
Author(s):  
James E. Heubi ◽  
James V. Higgins ◽  
Eric A. Argao ◽  
Rosa I. Sierra ◽  
Bonny L. Specker

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