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Low NO bioavailability in CCl4cirrhotic rat livers might result from low NO synthesis combined with decreased superoxide dismutase activity allowing superoxide-mediated NO breakdown: A comparison of two portal hypertensive rat models with healthy controls
© Van de Casteele et al; licensee BioMed Central Ltd. 2003
- Received: 29 August 2002
- Accepted: 10 January 2003
- Published: 10 January 2003
In cirrhotic livers, the balance of vasoactive substances is in favour of vasoconstrictors with relatively insufficient nitric oxide. Endothelial dysfunction has been documented in cirrhotic rat livers leading to a lower activity of endothelial nitric oxide synthase but this might not be sufficient to explain the low nitric oxide presence. We compared the amount of all nitric oxide synthase isoforms and other factors that influence nitric oxide bioavailability in livers of two portal hypertensive rat models: prehepatic portal hypertension and carbon tetrachloride induced cirrhosis, in comparison with healthy controls.
Endothelial nitric oxide synthase was the solely detected isoform by Western blotting in all livers. In cirrhotic livers, the amount of endothelial nitric oxide synthase protein was lower than in healthy controls, although an overlap existed. Levels of caveolin-1 messenger RNA were within the normal range but endothelin-1 messenger RNA levels were significantly higher in cirrhotic livers (p < 0.05). A markedly lower superoxide dismutase activity was observed in cirrhotic livers as compared to healthy controls (p < 0.05).
In contrast to prehepatic portal hypertension, cirrhotic livers had decreased endothelial nitric oxide synthase protein and enhanced endothelin-1 messenger RNA amount. We hypothesise that a vasodilator/vasoconstrictor imbalance may be further aggravated by the reduced activity of superoxide dismutase. Decreased activity allows enhanced superoxide action, which may lead to breakdown of nitric oxide in liver sinusoids.
- Nitric Oxide
- Cirrhotic Liver
- eNOS Protein
- Liver Cell Type
- Hepatic mRNA Level
The balance of vasoactive substances in cirrhotic livers is in favour of vasoconstrictors [1–3]. This contrasts with splanchnic and systemic vasodilatation characteristically seen in this condition [1, 2]. Nitric oxide (NO), prostacyclin and carbon monoxide are known intrahepatic vasodilating substances, whereas endothelin-1, superoxide (O2-), angiotensin-II, epinephrine and others act as vasoconstricting agents [1–6]. NO is produced by 3 different nitric oxide synthase (NOS) isoforms: neuronal NOS (nNOS), inducible NOS (iNOS) and endothelial NOS (eNOS) . The latter is in a normal liver clearly present in endothelial cells of portal venules, portal arterioles and central venules, as well as in sinusoidal endothelial cells [7, 8]. Other liver cell types such as hepatic stellate [9, 10], Kupffer cells  or hepatocytes [7, 9] do not express eNOS. A diminished hepatic activity of eNOS by about 30–50 % was documented in carbon tetrachloride (CCl4) induced cirrhosis [7–9, 11], in biliary fibrosis of the rat [9, 12] and in advanced human cirrhosis . This led to the concept that decreased hepatic NO bioavailability in case of cirrhosis is due to decreased NO synthesis [7, 9, 11–13]. The contribution of nNOS and iNOS to portal hypertension is not well studied . In the present study, we wanted to know which NOS isoform was the most abundant in rat livers in normal conditions and in two different models of portal hypertension: prehepatic portal hypertension and CCl4 cirrhosis.
Western blots of eNOS, iNOS and nNOS
The eNOS was the only NOS isoform detected in livers of all groups. The amount of eNOS protein in liver homogenates was similar in normal and PPVL rats (Fig. 2A), but was lower in CCl4 cirrhotic livers (Fig. 2A), although some overlap existed with healthy controls. This is in accordance with the variable severity of the cirrhosis in this model. The iNOS protein content was below the limit of detection in livers of healthy controls and the two groups with portal hypertension (Fig. 2B). The nNOS protein was not detected in any liver homogenate (Fig. 2C). In Western blots of iNOS and nNOS but not in those of eNOS, some atypical bands of smaller proteins were observed (data not shown).
Hepatic mRNA levels of caveolin-1 and endothelin-1
A large variation of caveolin-1 mRNA values was present in all groups. Levels in the two portal hypertensive groups were not significantly different from healthy control values (Table 2).
Levels of endothelin-1 mRNA in the PPVL group were comparable to those of healthy control rats (Table 2), but values of CCl4 cirrhotic livers were significantly and approximately 40-fold higher (p < 0.05 vs controls) (Table 2).
Hepatic SOD activity
SOD activity in liver homogenates of healthy controls was 15 (7) U/mg protein and it was 14 (3) U/mg protein in PPVL rats (Table 2). In CCl4 cirrhotic livers, SOD activity was significantly reduced to 10 (3) U/mg protein (p < 0.05 vs normal livers) (Table 2).
Hepatic malondialdehyde levels
Malondialdehyde, a marker of lipid peroxidation, ranged in normal livers from 2 to 20 pmol/mg liver (median 15) and similar values were measured in PPVL rats. In CCl4 cirrhotic livers, malondialdehyde levels were significantly elevated, with a median of 26 pmol/mg liver (range 6 to 130) (p < 0.05 vs normal livers) (Table 2).
The portal vein resistance in the PPVL rat model results from the mechanical stenosis laid around the extrahepatic part of the portal vein . In PPVL rats, we could not document any change in hepatic eNOS protein, endothelin-1 mRNA, caveolin-1 mRNA or SOD activity. Our findings suggest that the (atrophic) parenchyma in PPVL rats is not altering portal vein resistance importantly. In portal vein tissue below this stenosis, however, increased endothelin-1 levels have been documented and administration of endothelin-A receptor antagonists lowered the pressure in the prestenotic portal vein .
In the CCl4 cirrhotic model, eNOS activity is subnormal as reported by different groups [7–9, 11]. This could be due to several causes. In our CCl4 cirrhotic rats, the amount of eNOS protein itself was subnormal (Fig. 2A), which we confirmed by immunohistochemistry . Others did not find such a difference  but this might be related to differences in rat strains, degree of cirrhotic process or of the applied techniques, e.g., since they used an immunoprecipitation step before protein blotting . When eNOS spots on Western blots are very dense, densities do not correlate anymore with loaded protein amounts (own personal observation).
More important than eNOS protein amounts, is the understanding of eNOS enzymatic activity . The eNOS activity is inhibited by protein-protein interaction of caveolin-1 with eNOS in hepatic [7, 12] and extrahepatic vessels [14, 18]. Others cast doubt on the very localisation of caveolin-1 in hepatic endothelial cells . Caveolin-1 expression has been observed in hepatocytes, Kupffer cells and stellate cells as well . We admit that in the present study we could not clarify the cellular localisation of caveolin-1 nor caveolin-1/eNOS interaction with mRNA measurements. We documented a small but not significant increase of caveolin-1 mRNA in CCl4 cirrhotic livers (Table 2). If caveolin-1/eNOS interaction takes place in liver endothelial cells, our findings show that a clear-cut upregulation of caveolin-1 (as seen for endothelin-1 in Table 2) was not the case in CCl4 cirrhotic liver tissue. The significant increase of endothelin-1 mRNA in this model (Table 2) is compatible with reports from other groups [20, 21], where stellate cells  and hepatocytes  were identified as important endothelin-1 synthesising cells. An increased endothelin-1 synthesis together with changes in endothelin-A and B receptor density may be implicated in haemodynamic deteriorations [5, 34]. A (relatively) insufficient NO production will thus allow vasoconstrictor effects.
SOD activity enhances NO bioavailability by removing O2-, which otherwise could rapidly convert NO into peroxynitrite and other reactive nitrogen species [17–20, 23, 24, 35], as is given schematically in Fig 1. The observed decrease of SOD activity might allow higher intrahepatic O2- action. In the CCl4 cirrhotic rat liver, we hypothesise that enhanced intrahepatic O2- will further reduce the already low NO and this will further amplify vasoconstrictor supremacy . The observation that exogenously administered superoxide doubled portal pressure in the isolated perfused liver of a normal rat  supports this hypothesis. The antioxidative defence enzyme SOD is present in different isoforms in all liver cell types . Admittedly, we did not study SOD activity in particular liver cell types or in the vascular lumen (the latter regards the extracellular SOD isoform). SOD can easily interfere with NO and O2- released by endothelial cells [29, 36]. It is also known that activities of various SOD isoforms cannot easily be discriminated in rat liver tissue [36, 37].
Presumed vasoconstrictive properties of reactive oxygen species may have consequences in chronic liver diseases with regard to the study of superoxide dismutase mimetics as treatment for portal hypertension. A recent report showed that gene transfer of the extracellular SOD isoform was beneficial in rats with endothelial dysfunction related to arterial hypertension .
In conclusion, we found that eNOS was the major if not the sole NOS isoform in livers of normal, PPVL and CCl4 cirrhotic rats. In contrast to prehepatic portal hypertension, CCl4 cirrhotic livers had decreased eNOS protein and enhanced mRNA levels of endothelin-1 but not of caveolin-1. This vasodilator/vasoconstrictor imbalance might be further aggravated by a reduced SOD activity, which could lead to enhanced superoxide-mediated inactivation of NO in liver sinusoids. The resulting low NO is unable to counteract the enhanced endothelin-1 and this results in a strong vasoconstricting effect in CCl4 cirrhotic livers.
Livers used for NOS Western blots. Characteristics of normal and two types of portal hypertensive rats whose livers were used for the detection of NOS isoforms by Western blot in Fig. 2. Data are expressed as mean (SD).
(n = 14)
(n = 6)
(n = 11)
Body weight (g)
Liver weight (g)
PVP (mm Hg)
eNOS related parameters in rat livers: caveolin-1, endothelin-1, as well as SOD total activity and malondialdehyde levels.
(n = 9)
(n = 5)
(n = 9)
Body weight (g)
Liver weight (g)
Portal venous pressure (mm Hg)
cDNA dilutions still detecting caveolin-1 by RT-PCR
cDNA dilutions still detecting endothelin-1 by RT-PCR
SOD total activity (U/mg protein)
Malondialdehyde (pmol/mg liver)
Western blotting for nNOS, iNOS and eNOS
SDS/PAGE 7.5 % gel electrophoresis was run with diluted homogenates containing 30 μg of protein and with marker proteins (Sigma, St. Louis, USA) including a 120 kD protein, E. coli β-galactosidase. All protein concentrations were measured using the Bradford method (Bio-Rad Labs, Hemel Hempstead, UK) and with bovine serum albumin as standards. As positive controls were taken: a lysate of human aorta endothelial cells (Transduction Labs, Lexington, USA) for eNOS; a homogenate of rat brains for nNOS; and a liver of a rat given LPS 800 μg/kg IV (Sigma, St. Louis, USA) 6 hours before harvesting for iNOS. Samples of both portal hypertensive conditions and healthy controls were run simultaneously on the same gel. Two liver homogenate samples per liver were run. After blotting on a nitrocellulose membrane, blots were blocked overnight at 4°C. Blots were incubated for 2 hours with a mouse monoclonal antibody respectively against eNOS, nNOS or iNOS (Transduction Laboratories, Lexington, USA), dissolved at 1:1000 in buffer II (10 mM Tris-HCl pH 7.6, 0.1 M NaCl, Tween-20 at 0.1 %). Subsequently, blots were incubated with sheep anti-mouse IgG, horseradish peroxidase-labelled (Amersham, Bucks, UK), at 1:3000 diluted in 5 % skimmed milk powder blocking solution for one hour. After washing, detection reagents (ECL Western blotting system, Amersham, Bucks, UK) were added and blots were shortly exposed to an autoradiography film (Nen Life Science Products, Boston, USA) (Figs. 2-4) . To check for adequate protein loading and blotting, all blots were stained afterwards with Ponceau S red dye (Sigma, St. Louis, USA).
Hepatic mRNA levels of caveolin-1 and endothelin-1 with RT-PCR
Hepatic caveolin-1 or endothelin-1 mRNA levels were assessed semi-quantitatively with RT-PCR, using serial dilutions of cDNA as a measure for the amount of specific mRNA in the different livers. Briefly, total RNA was extracted in a single step procedure . The precipitated RNA was dissolved in 20-μl DEPC-treated water and the concentration was measured using the Ribogreen RNA quantitation kit (Molecular Probes, Eugene, USA), with ribosomal RNA as standard. One μg of this RNA was used for cDNA synthesis with M-MLV reverse transcriptase (GibcoBRL, Life Technologies, Merelbeke, Belgium) and random primers (Amersham Pharmacia Biotech, Little Chalfont, UK) in a volume of 20 μl, 1 hour at 37°C. The reaction was stopped by heating in boiling water for 1 min.
The PCR primer set used for the detection of rat caveolin-1 mRNA (access number Z 46614) was:
P18: 5'-CCG.GGA.ACA.GGG.CAA.CAT.CTA.CAA.GCC-3' positions 82–108;
M28: 5'-GCC.GTC.RAA.ACT.GTG.TGT.CCC.TTC.TGG-3' positions 251–277, resulting in a fragment of 195 bp. Note that R stands for [A,G].
The PCR primer set used for the detection of rat endothelin-1 mRNA (preproendothelin-1) (access number NM 612548) was:
P1: 5'-CAG.GTC.CAA.GCG.TTG.CTC.CTG.CTC.CTC.C-3' positions 328–355;
M2: 5'-CAC.CAC.GGG.GCT.CTG.TAG.TCA.ATG.TGC.TCG-3' positions 782–811, resulting in a fragment of 483 bp.
PCR determinations were performed on a dilution series of each sample. The first sample contained cDNA equivalent to 0.25 μg total RNA; each following sample was diluted to half the concentration of the previous one. The PCR mixture contained 5 μl of cDNA solution, 6.25 pmol of each primer, 0.2 μM of each dNTP, 1 U of Taq DNA polymerase adjusted by PCR buffer (10 mM Tris-HCl pH 8.3, 50 mM KCl, 2.5 mM MgCl2 and 0.01 % gelatin) in a final volume of 50 μl. Samples were overlaid with 100 μl mineral oil. PCR conditions were identical for both primer sets: denaturing 5 min at 95°C; 45 cycles of 1 min at 95°C, 45 sec at 58°C and 45 sec at 72°C; and a final step for 5 min at 72°C, after which the samples were stored at 4°C. Samples were analysed on a 2 % agarose gel. Samples of both portal hypertensive conditions and healthy controls were separated simultaneously on the same gel. The majority of the samples were amplified and analysed at least in duplicate. Results are given as the highest dilution that gave a positive signal on the gel (Table 2).
Hepatic superoxide dismutase (SOD) activity
SOD activity in liver homogenates in buffer I was diluted 400 times with buffer I and measured with a RANSOD kit (Randox Laboratories, Crumlin, UK) according to the manufacturer's instructions. In brief, xanthine oxidase generates O2-, which reacts with a chromogen to form a red formazan dye that is photometrically quantified. One SOD unit was defined as 55 % inhibition of dye formation. SOD activity was expressed as U/mg protein (Table 2).
Hepatic malondialdehyde levels
Determination of malondialdehyde was performed as published before . Briefly, liver homogenates in buffer I were run together with 1,1,3,3-tetraethoxypropane as standard and buffer I as blanks. After the addition of phosphoric acid and thiobarbituric acid, samples were heated at 80°C for 15 min. Longer and more intense heating created too much interference of sucrose  (own personal observation). Ice cooled reaction products were further separated by high performance liquid chromatography-reverse phase technique . The latter step is necessary to eliminate other substances that had reacted with thiobarbituric acid . Results are expressed as pmol malondialdehyde/mg liver wet weight (Table 2).
Data are given as mean (SD) or as median [range] for respectively normally and non-normally distributed data. We made comparisons of the 3 groups (normal, PPVL, CCl4 cirrhosis) by one-way-analysis of variance in case of normally distributed data with equal variances. If other cases, we used analysis of variance-on-ranks, where the sum of ranks of each group was compared. When significant differences between groups means were found, the Scheffe's post hoc test was performed to identify the groups. Significance level was always taken at α = 0.05. Statistical analyses were carried out with Sigma STAT 2.0 (Jandel Corporation, San Rafael, USA).
Written approval for the present experiments was obtained from the Ethical Committees for Animal Research of the Catholic University of Leuven, Belgium, and of the University of Berne, Switzerland.
This study was supported by grants from the Swiss National Foundation for Scientific Research to JR (n° JR-45349-95 and 63476.00) and from the Foundation for Scientific Research, FWO-Vlaanderen (n° b.0111.98) to FN.
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