1998
DOI: 10.1046/j.1525-1594.1998.06166.x
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Total Blood Exchange Suppresses the Early Stage of Liver Regeneration Following Partial Hepatectomy in Rats

Abstract: Despite its obscure and short effect, plasma exchange (PE) remains a mainstay in the treatment of liver disease. However, the question still remains as to whether or not PE suppresses the regeneration of the liver because PE deprives patients of hepatotrophic factors. The effect of PE, which could be a total blood exchange (TBE) in a syngeneic setting, on liver regeneration following a 68% partial hepatectomy (PH) was investigated in rats. In Group 1, 20 ml of blood from normal rats was infused while native bl… Show more

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Cited by 16 publications
(12 citation statements)
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“…Moreover, the PE procedure removed all elements of plasma, including some beneficial substances (such as HGF) for hepatocyte proliferation, which possibly suppresses hepatocyte proliferation [46]. We chose low-volume PE as the first Li-ALS step to efficiently utilise fresh plasma, avoid side effects, and reduce losing beneficial substances.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, the PE procedure removed all elements of plasma, including some beneficial substances (such as HGF) for hepatocyte proliferation, which possibly suppresses hepatocyte proliferation [46]. We chose low-volume PE as the first Li-ALS step to efficiently utilise fresh plasma, avoid side effects, and reduce losing beneficial substances.…”
Section: Discussionmentioning
confidence: 99%
“…During liver regeneration, quiescent hepatocytes undergo one or two rounds of replication and then return to a non‐proliferative state. Total blood exchange after partial hepatectomy suppresses the early stage of liver regeneration, 1 indicating the existence of factors important for regeneration in serum and blood cells. Although studies of factors involved in hepatic regeneration have been reported, most studies have been limited to animal models.…”
Section: Introductionmentioning
confidence: 99%
“…clearance of tacrolimus in control rats (9.22 ml/min/kg) and the reported blood flow of 55.2 ml/min/kg (Davies and Morris, 1993), and assuming lack of any change in the unbound fraction of tacrolimus, since red blood cells are primarily responsible for binding tacrolimus in blood (Venkataramanan et al, 1995) and since hematocrit does not change during hepatic regeneration (Eguchi et al, 1998;Kurata et al, 2000;Okano et al, 2001), the total body clearance of tacrolimus at the 24th h should have been, at most, 2.21 ml/min/kg. However, although the total body clearance of tacrolimus was significantly decreased 24 h after PHx, the magnitude was much less than what was predicted based on in vitro data.…”
Section: Tablementioning
confidence: 89%