|1.||Abe, Akihisa: 3 articles (04/2013 - 06/2009)|
|2.||Yamada, Hiroyuki: 2 articles (01/2011 - 06/2009)|
|3.||Kokuba, Hiroko: 1 article (04/2013)|
|4.||Soshilov, Anatoly A: 1 article (01/2012)|
|5.||El-Kadi, Ayman O S: 1 article (01/2012)|
|6.||Denison, Michael S: 1 article (01/2012)|
|7.||El Gendy, Mohamed A M: 1 article (01/2012)|
|8.||Moriya, Shota: 1 article (01/2011)|
|9.||Miyazawa, Keisuke: 1 article (01/2011)|
03/01/1987 - "In each group of experiments, there was a significant reduction in both the formation and elimination of harmol conjugates during hypoxia. "
03/01/1987 - "This study in the isolated perfused rat liver examines the effect of acute hypoxia on the hepatic elimination of harmol, a phenolic compound eliminated by conjugation without first undergoing oxidative metabolism. "
03/01/1987 - "Upon reoxygenation, T1/2 recovered to 4.2 +/- 0.5 min. Similar effects were observed in steady-state experiments, in which perfusate levels rose from 15.7 +/- 1.3 microM to 31.0 +/- 1.6 microM (P less than .005) during hypoxia, indicating a fall in harmol clearance of at least 50%. "
11/03/1992 - "Fasting increases the sensitivity of hepatic harmol glucuronidation to hypoxia."
04/01/1988 - "We conclude that nutritional state is important in determining the impact of hypoxia on harmol elimination by the liver. "
12/01/1991 - "2. The hepatic clearance (Cl) of harmol decreased from 7.8 +/- 0.4 ml/min in controls to 5.7 +/- 1.1 ml/min in the malaria-infected group in single-pass studies. "
12/01/1991 - "1. The effect of the erythrocyte stage of malaria infection on hepatic glucuronidation, biliary excretion and oxidation processes was investigated using harmol, salbutamol, taurocholate and propranolol. "
|3.||Hepatocellular Carcinoma (Hepatoma)
01/05/2012 - "Therefore, the aim of this study is to determine the effect of harmine and its main metabolite, harmol, on the dioxin-mediated induction of CYP1A1 in human HepG2 and murine Hepa 1c1c7 hepatoma cells. "
01/05/2012 - "Our results showed that harmine and harmol significantly inhibited the dioxin-mediated induction of CYP1A1 at mRNA, protein, and activity levels in a concentration-dependent manner in human and murine hepatoma cells. "
04/01/2013 - "In the present study, we found that harmol, a β-carboline alkaloid, induced autophagy and suppression of survivin expression, and subsequently induced apoptotic cell death in U251MG human glioma cells. "
04/01/2013 - "Harmol induces autophagy and subsequent apoptosis in U251MG human glioma cells through the downregulation of survivin."
06/01/2009 - "In this study, harmol and harmalol, which are beta-carboline alkaloids, were examined for their antitumor effect on human lung carcinoma cell lines, and structure-activity relationship was also investigated. "
06/01/2009 - "Harmol induces apoptosis by caspase-8 activation independently of Fas/Fas ligand interaction in human lung carcinoma H596 cells."
|1.||Cytochrome P-450 CYP1A1 (CYP1A1)
|6.||Fas Ligand Protein (Fas Ligand)
|7.||Caspase 8 (Caspase-8)
|9.||Taurocholic Acid (Sodium Taurocholate)
|10.||Messenger RNA (mRNA)
|1.||Protein-Restricted Diet (Diet, Protein Restricted)