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In vivo and ex vivo effects of propofol on myocardial performance in rats with obstructive jaundice
- Hong-Mei Ren†1,
- Li-Qun Yang†2,
- Zhi-Qiang Liu†3,
- Cai-Yang Chen2,
- Chi-Wai Cheung4,
- Kun-Ming Tao2,
- Jian-Gang Song2,
- Wu-Rong Chen1 and
- Wei-Feng Yu2Email author
© Ren et al; licensee BioMed Central Ltd. 2011
Received: 7 June 2011
Accepted: 28 December 2011
Published: 28 December 2011
Responsiveness of the "jaundiced heart" to propofol is not completely understood. The purpose of this study was to evaluate the effect of propofol on myocardial performance in rats with obstructive jaundice.
Male Sprague-Dawley rats (n = 40) were randomly allocated into two groups, twenty underwent bile duct ligation (BDL), and 20 underwent a sham operation. Seven days after the surgery, propofol was administered in vivo and ex vivo (Langendorff preparations). Heart rate, left ventricular end-systolic pressure (LVESP) left ventricular end-diastolic pressure (LVEDP), and maximal rate for left ventricular pressure rise and decline (± dP/dtmax ) were measured to determine the influence of propofol on the cardiac function of rats.
Impaired basal cardiac function was observed in the isolated BDL hearts, whereas in vivo indices of basal cardiac function (LVESP and ± dP/dt) in vivo were significantly higher in rats that underwent BDL compared with controls. With low or intermediate concentrations of propofol, these indices of cardiac function were within the normal physiologic range in both groups, and responsiveness to propofol was unaffected by BDL. When the highest concentration of propofol was administrated, a significant decline in cardiac function was observed in the BDL group.
In rats that underwent BDL, basal cardiac performance was better in vivo and worse ex vivo compared with controls. Low and intermediate concentrations of propofol did not appear to impair cardiac function in rats with obstructive jaundice.
Postoperative obstructive jaundice is associated with multiple organ dysfunction syndrome [1–3]. Specifically, the cardiovascular instability caused by defects in myocardial performance and vascular reactivity is thought to be an important mechanism in the pathophysiology of multiple organ dysfunction syndrome [4, 5]. In 1986, Green  reported impaired left ventricular performance in dogs with cholemia, and called this hepatic cardiomyopathy "jaundiced heart". The jaundiced heart is also characterized by defective vascular reactivity attributed to altered beta-adrenergic receptor signaling , membrane fluidity, and down regulation of cardiac beta-adrenoceptor density and affinity .
Propofol is a widely employed intravenous anesthetic used to induce and maintain anesthesia. It is characterized by rapid onset/offset of effect and rapid elimination from the body [8, 9]. However, propofol can also induce cardiovascular depression, manifested primarily by decreased arterial blood pressure  due to inhibition of the sympathetic nervous system , a negative inotropic effect , and reduced preload .
The effect of propofol on myocardial performance in patients with obstructive jaundice is unclear. Therefore, in the present study, 7-day bile duct ligation (BDL) was used as a model of obstructive jaundice to evaluate the effect of propofol on cardiac function in vivo. In ex vivo experiments, the direct effects of propofol on the isolated heart of BDL rats were assessed to exclude the vasodilator effect of propofol and the associated neurohormonal adaptation in vivo [14, 15].
This study protocol was approved by the Institutional Animal Care and Use Committee at the Second Military Medical University. Male Sprague-Dawley rats (250-300 g) were housed in a temperature and humidity-controlled environment with a 12-h light dark cycle. The rats received unlimited access to water and food. Food was removed from the cage 16 hours before initiating the experiments.
Forty rats were randomly allocated into two study groups: 20 underwent the BDL procedure, and 20 underwent a sham operation (control), according to Lee . Rats were anesthetized with pentobarbital sodium (40 mg/kg by intraperitoneal [i.p.] administration). After opening the abdominal cavity, the bile duct was ligated at a point proximal to the hilus and a point immediately distal to the entry of the bile duct into the duodenum. The bile duct was then severed between the ligatures. The sham operation was carried out in a similar manner, but did not include ligating and severing the bile duct. Seven days after the BDL and sham procedures, blood was obtained to assess total bilirubin and alanine aminotransferase levels.
In vivo experiment
For the in vivo experiments, all surgical procedures were performed under sterile conditions. On the seventh postoperative day, rats (BDL group, n = 10; sham-operated control group, n = 10) were anesthetized with sodium pentobarbital (40 mg/kg i.p.). After tracheotomy and tracheal intubation, mechanical ventilation (room air at 60-70 breaths/min) was provided with a Harvard Apparatus Rodent Respirator (Harvard Apparatus, Boston, MA). A heating pad was placed under the animal to keep the rectal temperature at 36°C ± 1°C. A 1-cm midline incision was made in the neck, and the right common carotid artery was exposed. A polyethylene cannula was inserted through the artery to the left ventricle. To monitor intraventricular pressure, the cannula was connected to a pressure transducer (RM6240B type; Chengdu Instrument Corp., China). A cannula connected to a microinfusion pump (Graseby 3500; Graseby Medical Ltd., Watford, UK) via a three-port switch was placed in the left jugular vein for propofol administration. After a 30-min stabilization period, rats received an intravenous injection of propofol (Diprivan 2%, AstraZeneca UK Ltd UK) The dose range used in our study encompassed the 50% effective dose for propofol as reported by Carmichael et al. . Doses of 300, 600 and 900 μg/kg per minute of propofol were administered by infusion (15 min each dose) to generate dose-response curves for heart rate (HR), left ventricular end-systolic pressure (LVESP), and maximal rate for left ventricular pressure rise and declining (± dP/dtmax ). HR and cardiac function indices were determined at the point of maximum response for each propofol dose.
Ex vivo experiment
Langendorff heart preparation (ML870B2 AD Instruments Ltd, Shanghai, China) was used to evaluate the effects of propofol on cardiac performance. The rats (BDL group, n = 10; sham-operated control group, n = 10) were anesthetized with sodium pentobarbital (40 mg/kg i.p.). The heart was removed from the thoracic cavity and placed in ice-cold Krebs-Henseleit bicarbonate buffer (pH 7.4) containing heparin sodium. The heart was rapidly mounted on a Langendorff perfusion system via the aorta. A cardiac catheter, with a latex saccule at the tip, was inserted from a cut in the left auricle of the left atrium to the left ventricle. The saccule was filled with water to maintain the left ventricular end-diastolic pressure (LVEDP) at 6 to 8 mmHg. The other end of the catheter was connected to a pressure transducer (MLT844; Shanghai, China). The average surrounding pressure was 70 to 80 mmHg. The perfusion medium was a modified Krebs-Henseleit bicarbonate buffer gassed with 95% O2 and 5% CO2 at atmospheric pressure and maintained at 37.5°C. The buffer was composed of 118 mmol/L NaCl, 4.7 mmol/L KCl, 1.2 mmol/L KH2 PO4 , 25 mmol/L NaHCO3 , 2.5 mmol/L CaCl2 , 11.0 mmol/L glucose, 0.5 mmol/L EDTA-Na2 and 1.2 mmol/L MgSO4 . Recorded parameters included HR, LVESP, LVEDP, (and ± dP/dtmax ). Effects of propofol (12.5, 25, and 50 μmol/L) were tested using a method described by Jacob et al . In rats that underwent 3-day BDL, Jacob  showed impaired basal cardiac contractility and reduced left intraventricular pressure using two preparations of pithed rats and isolated functioning hearts. When the aortic flow and left ventricular pressure were stabilized, data were acquired for 30 consecutive seconds prior to drug testing. Each drug concentration was tested for a period of 15 min.
Data analysis was performed with Prism version 4.0 (GraphPad Software; San Diego, CA). Responses of cardiac function to propofol are expressed as mean ± standard error of the mean (SEM) relative to baseline values (percentage). Group results were compared by Student's unpaired t-test or the chi-square test. In vivo and ex vivo myocardial performance data were compared by two-way repeated measure analysis of variance (ANOVA) followed by the post hoc Bonferroni test. A P-value of < 0.05 was considered significant.
Serum total bilirubin and alanine transaminase in the BDL group were significantly higher than those in the sham-operated control group (total bilirubin, 1.4 ± 0.2 vs 158.7 ± 10.8 mM/L, respectively; alanine transaminase, 28.1 ± 1.9 vs 150.0 ± 14.2 IU/L respectively)(P < 0.01).
In vivo cardiac function
In vivo baseline heart rate and cardiac function in the BDL group and sham control group
+dP/dtmax (mmHg s-1)
-dP/dtmax (mmHg s-1)
355.5 ± 12.7
110.1 ± 4.3
3.7 ± 0.4
2173.6 ± 82.3
1249.7 ± 92.6
105 ± 17
311.3 ± 16.7*
127.2 ± 6.4*
4.5 ± 0.5
3288.7 ± 112.3*
2512.8 ± 132.5*
109 ± 13
Ex vivo cardiac function
Ex vivo baseline heart rate and cardiac function in the BDL group and the sham control group
+dP/dtmax (mmHg s-1)
-dP/dtmax (mmHg s-1)
SO (n = 10)
254.5 ± 19.5
112.5 ± 6.9
4.8 ± 0.5
1469.2 ± 157.4
1117.5 ± 70.0
BDL (n = 10)
201.3 ± 13.5*
92.4 ± 5.4*
7.4 ± 0.3*
1146.0 ± 64.2*
954.3 ± 103.7*
In the present study, we could not confirm impaired cardiac performance in a rat model of obstructive jaundice because the in vivo and ex vivo results were inconsistent. However, an important and novel finding is that the inhibitory effects of propofol on myocardial function were comparable in rats that underwent BDL and rats that underwent the sham operation at low and intermediate doses (12.5 and 25 μmol/L). At the highest dose of propofol tested (50 μmol/L), stronger effects on cardiac function were observed in rats with obstructive jaundice.
A propofol concentration of 2 to 4 μM was clinically relevant according to a previous study , and researchers proved that higher than > 10 μM propofol in vitro might cause cardiovascular depression . To compare the hemodynamic effects of propofol between cholestatic rat hearts and controls, we use d relatively high concentrations (12.5, 25, and 50 μmol/L) of propofol ex vivo because propofol at < 10 μM did not suppress the KATP channel or display a myocardial depression effect . The present study did not confirm our hypothesis that propofol depresses myocardial performance in the jaundiced heart compared with the normal, healthy heart. This finding may be attributed to a number of factors. First, most animal and human studies have shown that propofol induces dose-dependent cardiovascular depression. Furthermore, clinically relevant concentrations of propofol do not significantly depress myocardial contractility and evidence suggests that its pharmacological properties may be due in part to enhanced sensitivity of the myofilaments to Ca2+, despite reduced uptake of Ca2+ uptake into the sarcoplasmic reticulum [22, 23]. Moreover, propofol is a cardioprotective agent and may protect the myocardium from injury such as that caused by ischemia-reperfusion [24, 25]. Inhibition of the mitochondrial permeability transition pore is a recently reported mechanism underlying the protective action of propofol on the myocardium [24, 26]. In addition, accumulation of bile acids is a causative factor for jaundiced heart . Bile acids exert negative chronotropic and inotropic effects on the heart via mitochondrial damage [12, 27]. These factors especially the enhanced sensitivity of the myofilaments to Ca2+ and the inhibition of the mitochondrial permeability transition pore, may protect against cardiovascular depression and account for the minimal responsiveness of BDL-treated rats to low and intermediate concentrations of propofol.
Another interesting observation was the opposite in vivo and ex vivo results of basal cardiac contractility in the BDL group. In the ex vivo experiments, hearts from the BDL-treated rats exhibited impaired contractility and a reduction in the maximum pressure in the left ventricle, whereas BDL-treated rats showed significantly increased LVSEP, +dP/dtmax and -dP/dtmax in vivo. The mechanism underlying this phenomenon is unclear, but may involve neural or humoral adaptations. Dabagh  reported increased concentrations of norepinephrine and epinephrine during the development of cholestasis. Poo  found elevated renin and angiotensin II at 1 week after establishment of obstructive jaundice in rats. In our in vivo experiments, increased LVSEP, +dP/dtmax and -dP/dtmax , were associated with myocardial contractility, suggesting up regulation of the sympathetic nervous system. In addition, LVEDP which directly relates to the cardiac preload might remain unchanged possibly not owing to the depletion of body fluid in obstructive jaundice [30, 31]. However, the lower heart rate may be caused in part by accumulated bile acids, which impair cardiac function by affecting calcium uptake from the sarcoplasmic reticulum [32, 33]. Recent research has focused on the overproduction of nitric oxide, which results in bradycardia after BDL [34, 35]. Despite enhanced cardiac contractility in vivo, our experiment showed that a high dose of propofol produced stronger inhibition of cardiac function in BDL-treated rats, unmasking latent cardiac dysfunction. These results are consistent with those of previous studies reporting that BDL-treated rats show hemodynamic instability .
There are also limitations in our study. To assess left ventricular inotropism, three load-dependent indices of left ventricular contractility (LVESP, LVEDP, and ± dP/dtmax ) were used. It must be underscored that these indices may also be influenced by left ventricular loading conditions . Load-independent indices of left ventricular contractility, such as construction of pressure-volume curves in both systole and diastole would greatly enhance the validity and interpretation of our results. It would enable more specific measurement of the left ventricular performance independent of both loading conditions and HR . Thus, the data of our study must be interpreted with caution when using propofol at mild to intermediate doses in obstructive jaundice.
In conclusion, the present study demonstrates that obstructive jaundice impairs cardiac function ex vivo but enhances cardiac performance in vivo. Propofol depresses cardiac parameters at low and intermediate doses to a similar degree in BDL-treated and sham-operated rats. However, at a high dose, propofol may cause exaggerated cardiac depression in jaundiced rats. Our study suggestes that propofol is a safe alternative anesthetic agent in patients with obstructive jaundice and normal cardiac function at low and intermediate doses.
We gratefully acknowledge the National Natural Science Foundation Committee of China (Grant No. 81072625, 81170427) and Shanghai Municipal Education Commission Foundation (Grant No.11ZZ73) for their financial support.
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