- Open Access
Aqueous fish extract increases survival in the mouse model of cytostatic toxicity
© Omerovic et al; licensee BioMed Central Ltd. 2008
- Received: 12 June 2008
- Accepted: 04 December 2008
- Published: 04 December 2008
Treatment of cancer patients with anthracycline antibiotic doxorubicin (DOX) may be complicated by development of acute and chronic congestive heart failure (CHF), malignant arrhythmias and death. The aim of this study was to test whether an aqueous low molecular weight (LMW) extract from cod muscle decreases acute mortality in the mouse model of acute CHF caused by DOX.
A LMW fraction (<500 Da) of the aqueous phase of cod light muscle (AOX) was used for treatment of male BALB/c mice (~25 g, n = 70). The animals were divided into four groups, DOX + AOX (n = 20), DOX + saline (NaCl) (n = 30), NaCl + AOX (n = 10) and NaCl only (n = 10). Echocardiography was performed in the separate subgroups (DOX treated n = 6 and controls n = 6) to verify the presence and the grade of acute CHF. The cod extract was delivered by subcutaneously implanted osmotic minipumps over the period of 2 weeks. High-dose injection of DOX was administered to randomly selected animals. The animals received single intraperitoneal injection of DOX (25 mg/kg) and were followed over two weeks for mortality.
Mortality rate was 68% lower (p < 0.05) in the mice treated with the extract. The analyses of cod extract have shown strong antioxidative effect in vitro.
The aqueous LMW cod muscles extract decreases mortality in the mouse model of DOX induced acute CHF. This effect may be mediated by cardioprotection through antioxidative mechanisms.
- High Performance Liquid Chromatography
- Acute Heart Failure
- Total Amino Acid
The anthracycline antibiotic doxorubicin (DOX) is one of the most effective antitumor agents against human malignancies such as leukemia, lymphomas and many solid tumors [1–3]. However, the treatment of cancer patients with DOX may be complicated by deleterious side effects. One of the most feared side effects of DOX is a direct damage to the heart which may lead to the development of acute and chronic congestive heart failure (CHF), malignant arrhythmias and death [4, 5]. The acute form of cardiotoxicity may occur within a week of the treatment and is not dose-depended, indeed, it may occur after a single dose of the agent. On the other hand, the incidence of the chronic CHF at specific cumulative doses of doxorubicin include 0.4% at 400 mg/m2 of body surface area, 7% at 550 mg/m2, and 18% percent at 700 mg/m2 . Electrophysiologic abnormalities are frequent and are detected as ECG changes in 20–30% of the patients in form of non-specific ST and T wave changes, T wave flattening, decreased QRS voltage and/or prolongation of the QT interval. Arrhythmias, including ventricular and supraventricular tachycardias are seen in 0.5–3% of patients with overall incidence of 0.7% . Many different cardioprotective agents have been tested for prevention of DOX toxicity experimentally and clinically but with limited success. Considering the essential role of iron and the doxorubicin-iron complex, iron chelators have been developed against cardiotoxicity where dexrazoxane was found to be the most promising drug. Myocardial damage is a consequence of direct DOX interference with important intracellular homeostatic processes primarily mediated by increased intracellular oxidative stress. Intrinsic antioxidative systems in the cells are normally able to reduce the damage caused by oxidative stress. Compared to other organs, however, the heart has inherently lower potential to protect itself from the free radicals due to the limited number of anti-oxidative systems in the cardiomyocytes. It is therefore hypothesized that treatment with antioxidants may play an important role in preventing myocardial damage. The mouse model of acute DOX toxicity is a simple and readily available small animal model particularly suitable for screening studies for different cardioprotective interventions[10, 11]. In the recent years, there has been an increased research interest to develop cardioprotective and other pharmacological therapies from natural sources like animals and plants of marine origin. A well known example of such a promising clinical application in the field of cardiovascular medicine are the fish-derived long chain n-3 polyunsaturated fatty acids[12, 13]. There is evidence that also aqueous fish-derived substances, such as taurine, have cardioprotective effects. It has been speculated that these observations are caused by a radical scavenging mechanism. We hypothesize that aqueous fish muscle extract may improve survival in mouse model of acute heart failure.
The Animal Ethics Committee of the University of Göteborg approved the animal experiments. Male BALB/c mice (B&K Universal AB) weighing ~25 g were used in all experiments. Fresh whole cod (Gadus morhua) was obtained from Leröy Allt i Fisk (Göteborg, Sweden).
Preparation of extract from cod muscle
The cod was manually filleted and the light muscle was separated from skin and dark muscle. The light muscle was minced, packed in 200 ml polypropylene centrifuge bottles (200 g in each) and centrifuged at 15 000*g for 2 h at 4°C. The supernatant (press juice) was filtered through a filter paper (1010, Munktell's, Swedish Filter paper, Grycksbo pappersbruk AB, Sweden) and frozen immediately at -80°C. Using a stirred 400 ml Amicon ultra filtration cell (Model 52, Amicon Corporation, Danvers, MA, USA), 50 ml of thawed cod muscle press juice was filtered through a 500 Da ultrafiltration membrane (Millipore Corporation, Bedford, MA, USA) at 50 psi and 4°C. The first 25 ml of filtrate were collected and the pH was adjusted to 7.2 with 1 M NaOH. The filtrates were then immediately frozen at -80°C.
To evaluate whether the cod extract may be delivered subcutaneously without provocation of an inflammatory response, three animals were treated with the extract delivered by subcutaneously implanted osmotic pumps (Alzet, Durect Corp., Cupertino, USA, Model NO. 2002). The animals were followed up for 10 days and were inspected for signs of skin irritation and possible abscess formation. No signs of inflammation were found in the region after 10 days of follow-up.
One day after injection of DOX, echocardiography was performed in the subgroup of DOX treated mice (n = 6) and compared to the normal animals (n = 6). The purpose of this examination was to validate the model of acute DOX-induced cardiotoxicity i.e. to detect and measure the extent of cardiac damage. The examination was performed according to the previously described method. Echocardiographic images were obtained using a commercially available ultrasound system (ATL, Philip Medical System, Best) equipped with a 15 MHz linear transducer.
Analysis of ATP, ADP and AMP
The concentrations of myocardial ATP, ADP, and AMP were determined by high performance liquid chromatography (HPLC) from the animals that have survived 2 weeks according to the method previously described. The heart was explanted and immediately frozen in liquid nitrogen. The samples were maintained in a -134°C until final analysis. After preparation of the samples, the metabolites were separated after polarity in a column (Phenomenex® Luna 5 u C18 colonn) and analyzed on standard HPLC system (Gynkotek, Germering Germany).
Analysis of moisture content, pH and conductivity
The moisture content of the cod extract was measured using a HA300 Moisture Balance (Precisa balance 310 M, Zurich, Switzerland) (n = 2). The moisture results were expressed as percentage of wet weight. A Hamilton double pour electrode (Hamilton Double Pore, Bonaduz, Switzerland) in conjunction with a pH-meter (Radiometer analytical PHM210, Villeurbanne Cedex, France) was used for pH measurements. Conductivity was measured with a conductivity meter (CDM 210, Meter Lab, Radiometer Analy SAS, Villeurbanne Cedex, France).
Analysis of protein content
Total protein measurements of the cod extract were done according to Lowry et al (n = 2). Protein content was expressed as mg/mL of sample.
Analysis of total lipids
The method described by Lee et al was used to determine the total lipids in the cod extract using chloroform and methanol (1:1) as the extraction solvent (n = 2).
Analysis of ascorbic acid and uric acid
Ascorbic acid and uric acid of the cod extract was analyzed with HPLC using an electrochemical detector, with modifications according to Gunnarsson et al.  (n = 3). Both ascorbic acid and uric acid results are expressed as μM.
Analysis of amino acids
Total amino acids, free amino acids and some di-peptides like carnosine and anserine in the cod extract were analyzed with HPLC according to Fontaine et al.  (n = 2). Results were expressed as g/kg.
Analysis of the capacity of the cod extract to scavenge peroxyl radicals and to prevent ROS formation from human monocytes
The antioxidative capacity of the cod extract was analyzed quantitatively in vitro. These tests were based on the measurement of capacity to scavenge peroxyl radical activity using the Oxygen Radical Absorbance Capacity (ORAC) test and to scavenge reactive oxygen species (ROS) produced by phorbol myristate acetate (PMA) in stimulated human monocytes. The ORAC test, the method for isolating monocytes from human blood, and the method for analyzing whether the cod extract could prevent phorbol myristate acetate (PMA) initiated ROS formation of the monocytes is described by Gunnarsson et al. In brief, the ROS-preventing effect of the cod extract was analyzed as a relative reduction in the isoluminol-enhanced chemiluminescence (CL) signal given by the monocyte-derived ROS. Thus, the CL-signal given by the monocytes in the presence of the cod extract was compared with a control assay where no extract was added.
Computer software (StatView 5.0.1) was used to perform standard statistical procedures. Mortality rate was tested using a 2 × 2 contingency table. Fisher's PLSD (Protected Least Significant Difference) test proceeded by one-way analysis of variance (ANOVA) was applied to detect significant differences between different treatments for interactions defined in advance. The value p < 0.05 was considered as statistically significant. All data are presented as mean ± SEM.
All animals treated with DOX have shown lower BW (data not shown), appeared weak and lethargic. At necropsy, the most prominent gross pathologic change in the mice treated with DOX was excessive amounts of pericardial, pleural and peritoneal fluid indicating the presence of systemic as well as local toxic effect. On a gross pathological cardiac examination the hearts of the DOX treated animals were enlarged and there were signs of pericarditis with multiple adhesions of connective tissue formed between the pericardium and the inner thoracic wall. Furthermore, the epicardial surface was rich in areas of local fibrosis. These signs were not present in the control animals. No difference in the BW was found between the DOX + AOX and the DOX + NaCl groups. The DOX + AOX mice had less pronounced accumulation of pericardial, pleural and peritoneal fluid compared to the DOX + NaCl mice.
Analyses of myocardial purine nucleotides
Myocardial content of purine nucleotides determined by HPLC
DOX + AOX (n = 8)
16.2 ± 0.6
9.2 ± 0.8
2.7 ± 0.5
DOX + NaCl (n = 4)
18.6 ± 1.3
9.0 ± 0.3
2.5 ± 0.5
AOX + NaCl (n = 10)
16.2 ± 0.5
10.0 ± 0.4
2.8 ± 0.3
NaCl (n = 10)
15.3 ± 0.5
10.0 ± 0.3
3.0 ± 0.2
DOX (n = 6)
4.5 ± 0.2*
3.2 ± 0.2*
28 ± 2*
2.3 ± 1.4*
322 ± 21*
Control (n = 6)
3.7 ± 0.04
2.1 ± 0.07
43 ± 2
14 ± 1.6
406 ± 22
Compositional analyses of the cod extract
Compositional data and ORAC data of the LMW (< 500 Da) fraction of cod press juice.
Cod extract (<500 Da)
Dry Matter % (n = 2)
Native pH (n = 2)
Conductivity (mS/cm) (n = 2)
Total lipids % (n = 2)
Total protein (mg/mL) (n = 2)
Ascorbic acid (μM) (n = 3)
4.30 ± 0.54
Uric acid (μM) (n = 3)
0.34 ± 0.004
ORAC (mmol Trolox equivalents/l sample) (n = 8)
1.17 ± 0.06
Antioxidant testing of the cod extract using ORAC
The main results of the study could be summarized as follows: The LMW cod muscle aqueous extract decreased the mortality rate in mice following DOX-induced acute CHF. The extract is characterized by pronounced free-radical scavenging effects in vitro.
To the best of our knowledge, this is the first study to demonstrate the beneficial effect of an aqueous fish extract on survival rate in an in vivo animal model of acute heart failure. Cardioprotection has been in the research focus for many years. Different pharmacological and non-pharmacological strategies have been proposed to decrease myocardial damage e.g. during ischemia-reperfusion injury and cardiotoxicity. However, only few experimental interventions have been translated into a clinical practice and with a limited success. Several studies have shown beneficial cardiovascular effects of fish and fish derived substances. By far the best known are the long chain n-3 polyunsaturated fatty acids[12, 13]. These fatty acids may enter the cellular membrane and alter membrane functions resulting in, e.g., antiarrhythmic effects. Recent evidence indicates that dietary supplementation with fish oil preserves normal vasomotion of atherosclerotic coronary arteries and reduces damage to the myocardium after ischemia and reperfusion in animal models[23, 24]. Much less is known whether aqueous components of fish, e.g. proteins, peptides, amino acids and other organic acids may protect the heart. On a wet weight basis, the aqueous phase usually contribute to 95–99.5% of the total edible parts of seafoods. Indeed, the results of the present study provide the evidence that also aqueous fish-derived compounds may play an important role in cardioprotection.
Composition of total amino acids in Cod LMW-PJ (<500 Da).
Average g/L sample
Cod LMW-PJ (<500 Da)
0.5 ± 0
0.5 ± 0
0.3 ± 0
0.2 ± 0
Composition of free amino acids and certain dipeptides in Cod LMW-aqueous extract (<500 Da).
Cod extract (<500 Da)
0.55 ± 0
0.07 ± 0.01
0.04 ± 0
0.03 ± 0
0.04 ± 0
0.035 ± 0.005
0.325 ± 0.005
0.295 ± 0.005
0.04 ± 0
0.02 ± 0
0.04 ± 0
0.175 ± 0.015
0.08 ± 0
0.095 ± 0.005
0.09 ± 0
There are some limitations that deserve to be mentioned. We have not compared the efficacy of the cod muscle extract to other known cardioprotective agents such as dexrazoxane. We have not demonstrated specific cardioprotective effects of the extract in terms of cardiac function (echocardiography) or tissue structure (pathohistology). Furthermore, our study does not provide the answer to whether the survival benefit is mediated by few compounds in the extract (such as taurine and anserine) or by multiple compounds optimally mixed in this preparation.
In conclusion, the aqueous LMW cod muscles extract decreases mortality in the mouse model of DOX induced acute CHF. This effect may be mediated by cardioprotection through antioxidative mechanisms.
This work was supported by HM Sultan Qaboos Research Trust Fund (Project no. SR/AGR/FOOD/05/01), the Swedish Research Council (Grant K2005-73X-00536-41A), Västra Gotaland Region, National Board of Fisheries (Dr 223-2451-01), Sweden (EU structural funds), Sahlgrenska University Hospital, Goteborg University, and the Swedish Heart and Lung Foundation. We thank Ulrika Paija, Gudjon Gunnarsson and Thippeswamy Sannaveerappa for help with the animal experiments, the antioxidant tests and the compositional analyses respectively.
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