Literature DB >> 2687528

Thromboxane as a possible hepatotoxic factor increased by endotoxemia in obstructive jaundice.

T Hanai1, J Yura, K Ogino, K Hori, T Suzuki.   

Abstract

In a study using rats, we investigated whether liver damage induced by endotoxemia in obstructive jaundice is associated with thromboxane (TX) in order to acertain whether its vasoconstrictive and platelet aggregating properties play a role in reducing liver blood flow. The rats were divided into the following 5 groups; a control group, an endotoxin (Et) group, a bile duct ligation (BDL) group, a bile duct ligation and endotoxin (BDL + Et) group and an OKY046 (Thromboxane synthetase inhibitor) treated bile duct ligation + endotoxin (OKY-BDL + Et) group. The blood TXB2 levels in the Et, BDL and BDL + Et groups were higher than those in the control group. The liver TXB2 levels in the Et and BDL + Et groups were also higher than those in the control group. Liver phospholipids and liver blood flow decreased in the BDL + Et group, whereas in the OKY-BDL + Et group they returned close to the control group levels by decreasing the TXB2 levels in both the liver and blood to normal. These results suggest that the high level of TX in the blood and liver tissue may further aggrevate the liver during endotoxemia in obstructive jaundice by inhibiting liver blood flow.

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Year:  1989        PMID: 2687528     DOI: 10.1007/bf02471663

Source DB:  PubMed          Journal:  Jpn J Surg        ISSN: 0047-1909


  21 in total

1.  The mechanism of suppression of renal function in patients and rabbits with jaundice.

Authors:  K Ozawa; T Yamada; J Tanaka; M Ukikusa; T Tobe
Journal:  Surg Gynecol Obstet       Date:  1979-07

Review 2.  The role of lysosomes in circulatory shock.

Authors:  A M Lefer
Journal:  Life Sci       Date:  1976-12-15       Impact factor: 5.037

3.  Biliary obstruction and host defense failure.

Authors:  J M Holman; L F Rikkers
Journal:  J Surg Res       Date:  1982-03       Impact factor: 2.192

4.  Accelerated phospholipid degradation and associated membrane dysfunction in irreversible, ischemic liver cell injury.

Authors:  K R Chien; J Abrams; A Serroni; J T Martin; J L Farber
Journal:  J Biol Chem       Date:  1978-07-10       Impact factor: 5.157

5.  Vasoconstrictor effect of thromboxane A2.

Authors:  J Svensson; B B Fredholm
Journal:  Acta Physiol Scand       Date:  1977-11

6.  Arterial walls generate from prostaglandin endoperoxides a substance (prostaglandin X) which relaxes strips of mesenteric and coeliac ateries and inhibits platelet aggregation.

Authors:  S Bunting; R Gryglewski; S Moncada; J R Vane
Journal:  Prostaglandins       Date:  1976-12

7.  Synthesis of prostanoids and cyclic nucleotides by phagocytosing rat Kupffer cells.

Authors:  M Birmelin; K Decker
Journal:  Eur J Biochem       Date:  1984-07-16

8.  Changes in the levels of endogenous coenzyme Q homologs, alpha-tocopherol, and glutathione in rat liver after hepatic ischemia and reperfusion, and the effect of pretreatment with coenzyme Q10.

Authors:  S Marubayashi; K Dohi; K Yamada; T Kawasaki
Journal:  Biochim Biophys Acta       Date:  1984-01-24

9.  Role of lipid peroxidation in tissue injury after hepatic ischemia.

Authors:  E H Silver; S Szabo
Journal:  Exp Mol Pathol       Date:  1983-02       Impact factor: 3.362

10.  Thromboxanes: a new group of biologically active compounds derived from prostaglandin endoperoxides.

Authors:  M Hamberg; J Svensson; B Samuelsson
Journal:  Proc Natl Acad Sci U S A       Date:  1975-08       Impact factor: 11.205

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