2, 4 If patients do not respond to these drugs, experimental approaches may be applied. The molecular absorbance recirculating system (MARS) is an extracorporeal liver dialysis system capable of removing mainly Wnt inhibitor albumin-bound molecules, such as bile salts, bilirubin, ammonia, and other amphiphilic toxins. MARS therapy has been shown to effectively alleviate intractable pruritus of cholestasis in patients who do not respond to any medicinal therapy.2, 4, 5 Nasobiliary drainage transiently relieves severe pruritus

in benign recurrent intrahepatic cholestasis (BRIC)6 and primary biliary cirrhosis (PBC) patients7 who do not respond to standard antipruritic treatment.2, 4 However, pruritus may even become refractory to all medical treatments and can be an indication for liver transplantation, even in the absence of liver failure.4 By functional screening of sera of patients with cholestasis

suffering from pruritus on neuronal cells, we recently identified lysophosphatidic acid (LPA) this website as a potent neuronal activator.8 Serum levels of this phospholipid were increased in patients with cholestasis that suffered from pruritus. Circulating LPA is formed by a lysophospholipase D, called see more autotaxin (ATX), which hydrolyzes the choline group from lysophosphatidylcholine (LPC).9 In mice, the amount of circulating LPA depends on serum ATX activity.10 In line with the observed increase in LPA, ATX activity was higher in sera of patients with pruritus with cholestatic disorders, compared to those without pruritus. Furthermore, itch intensity highly correlated with ATX activity. Intradermal injection of LPA caused a dose-dependent scratch response in mice.8 ATX was initially identified as a cell motility factor, which is overexpressed in various tumors and is involved in the proliferation and generation of metastases.11

The effects of ATX are largely mediated by the enzymatic formation of LPA, which activates at least six different G-protein-coupled receptors.9, 11 ATX is also essential for angiogenesis, neuronal development, and lymphocyte homing,10 and LPA mediates the initiation of neuropathic pain, hair growth, and embryo implantation.9 Here, we studied whether increased serum ATX activity is specific for pruritus of cholestasis. We also aimed to investigate the effect of various therapeutic interventions, such as treatment with colesevelam, rifampicin (RMP), MARS, and nasobiliary drainage on ATX activity. Finally, the effects of RMP on ATX expression were studied in vitro.