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Association of long-term consumption of repeatedly heated mix vegetable oils in different doses and hepatic toxicity through fat accumulation

Lipids in Health and Disease volume 19, Article number: 69 (2020) Cite this article

Abstract

Background

Hepatic diseases are one of the chief reasons for worldwide morbidity and mortality. The increased incidence in Asian countries is driving researchers to explore preventive ways from nature. It is more practical to go with healthy routine edibles like vegetable oils to avoid environmental and chemical hepatic injuries. With the use of thermally oxidized oils overproduction of reactive oxygen species (ROS) with overwhelmed cellular antioxidants defense system results in oxidative stress, the known cause of cardiovascular diseases (CVDs), cancers and neurodegenerative disorders. Little is investigated about the effect of daily used oxidized cooking oils on hepatic function changes with oxidative stress especially in the animal model that mimics the human situation.

Methods

In this study, healthy adult male rabbits of local strain were divided into 4 groups (n = 12). First, two sets of rabbits were treated with 1 and 2 ml/kg/day of repeatedly heated mix vegetable oils (RHMVO) respectively. The third set of rabbits was given 1 ml/kg/day of single time heated mix vegetable oils (STHMVO) and the fourth set of rabbits served as controls and fed with normal rabbit diet to for 16 weeks. Serum liver function markers including total-protein, albumin, serum glutamic-oxaloacetic transaminase (SGOT), serum glutamic-pyruvic transaminase (SGPT) and alkaline phosphatase (ALP) along with the activity of hepatic antioxidant-enzymes including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) and malondialdehyde (MDA) for lipid peroxidation were compared among different groups of rabbits. Histopathological examination was performed for all four groups.

Results

Significantly (p < 0.05) elevated hepatic enzymes and MDA levels, with lower total protein, serum albumin, GPx, SOD and CAT levels were found in high and low doses RHMVO treated groups, in comparison to control. In the STHMVO group, all mentioned markers were insignificantly changed. Accumulation of liver fat in low and high dose oil-treated groups was further confirmed under the microscopic examination of liver tissues, presented significant fat accumulation in liver tissues, in addition, 40–60% increased oxidative stress compared to control, in a dose-dependent manner.

Conclusions

These results conclude that consumption of thermally oxidized mix vegetable oils for longer duration can impair the liver function and destroy its histological structure significantly through fat accumulation and oxidative stress both in high as well as low doses.

Background

Vegetable oils are an essential part of the human diet, being the major lipid and energy source, which also serve as an integral part of bio-membrane and hormonal building block [1] Cooking oils are mostly consumed in food processing to enhance palatability of the food. In households and at the commercial level, to minimize the cost and maximize profits, cooking oil is often reused, which is common practice in South Asian countries like Pakistan. Several studies have reported the harmful effect of thermal oxidation on cooking oils and processed food [2], but regardless of all these studies, the practice seems to continue.

Physico-chemical characteristics of the cooking oils changes when heated beyond a certain limit and several chemical reactions take place in moisture and air presence, oils degenerate and produce volatile substances, unwanted monomers, polymers, isomers and free radical [3]. In cooking oil fatty acids (FAs) naturally exist in the cis-isomer form, but during thermal oxidation they convert into trans-isomers, possessing physical properties similar to saturated FAs [2]. Several animal studies demonstrate that consumption of repeatedly heated oils increased the risk of cardiovascular diseases (CVDs) like hypertension with reduced vasorelaxation responses [4], endothelial malfunction [5], lipid peroxidation [6], atherosclerosis [7], oxidative stress [8], genotoxicity [9], carcinogenicity and lower glucose absorption [10].

Trans-isomer FAs consumption has been associated with the occurrence of metabolic syndrome (obesity, CVDs, insulin resistance along with systemic inflammation) [11]. Systemic inflammation induced imbalance of prostaglandins causes thrombogenesis [12] and activation of systemic inflammatory responses [13]. Oxidative stress and damage is a chief contributing factor to the development of CVDs [14]. About three-quarters of all deaths due to CVDs were only reported from countries with low to middle income [15]. The South Asian population has the highest known rate of coronary artery diseases with the predicted addition of up to about twenty-four million by 2035 [16]. The liver, colorectal & stomach cancers are among the top five frequently detected reasons for deaths due to cancer [17].

The liver is the vital part of our body which is responsible for detoxification of toxic metabolites, protein synthesis and productions of compounds required for food digestion [18]. Excessive free radicals are known to cause liver damage and may result in hepatitis, cirrhosis and hepatic tumor [19]. Thermally oxidized oils are the most significant source of oxidative damage in our body if used regularly. Hepatic problems are among the leading reasons for worldwide morbidity and mortality [20]. A highly increased number of hepatic diseases in Asian countries [21, 22] is also driving researchers to explore the natural therapeutic and protective agents for hepatic problems [23]. However, little is investigated about the effect of daily used oxidized cooking oils on changes in hepatic functions with induced-oxidative-stress [24] especially in the model that mimics the human situation.

Overproduction of reactive oxygen species (ROS), like hydrogen peroxide (H2O2), superoxides and hydroxyl, with overwhelming cellular antioxidants defense system results in oxidative stress [25,26,27], the known cause of CVDs, cancers and neurodegenerative disorders [28]. ROS are removed from the biological system through a number of enzymes and non-enzymatic defense mechanisms [29]. In enzymatic eradication, superoxide anions are converted to H2O2, and further rapidly degrade H2O2 to H2O by first line antioxidants defense system of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) [29, 30]. Furthermore, oxidative stress-induced uncontrolled lipid peroxidation may also result in cell injury through protein inhibition and DNA damage [31, 32]. Malondialdehyde (MDA), a stable end product of lipid peroxidation, is used for measuring the collective lipid peroxidation. Thus, based on the previous studies, SOD, CAT and GPx, MDA have been studied as biological markers of oxidative stress and lipid peroxidation [30, 33].

Presently, several animal models have been used to study fat-induced pathological conditions, like mice, zebrafish and, rats. To study the effect of differently treated vegetable oils on lipid metabolism and oxidative stress, the selection of experimental animal models is very critical to conduct basic research and develop a study tool. In this respect, to study human fat metabolism the rabbit has become the most appropriate animal model because of rabbits’ unique features of lipid metabolism similar to humans [34,35,36].

Previous animal studies have reported that 57% caloric requirements from the fat diet resulted in hepatic steatosis, damage and non-alcoholic fatty liver disease [37,38,39]. In all these studies a single oil was investigated not the blend of thermally oxidized vegetable oils. In Pakistan commercially available oils are mostly a blend of two or more edible oils and the most common available blend of an equal ratio of olive, canola and sunflower oils was focused in this study, to have the model that mimics the human situation. To our information, no such effort has been reported from Karachi, Pakistan, in particular. We designed this animal model to investigate the development of hepatic toxicity with induced oxidative-stress through the long-term consumption of repeatedly heated mix vegetable oils (RHMVO) in high and low doses in comparison with single time heated mixed vegetable oils (STHMVO) and control, in rabbits [34].

Methods

Oil samples preparation

Standard food-grade canola, sunflower and olive oils (7 l of each) were purchased from the Karachi local market. Each oil was thermally treated for a total of 45 min till 330 to 360 °F (beyond the smoke point) [40, 41], then cooled to room temperature and mixed in equal ratio (1:1:1) then sufficient quantity of oil labeled as STHMVO. The remaining oil mixture was heated in the same manner for the coming 9 days (one time each day) and then cooled to room temperature. Every day before heating, the oil level was adjusted in the pan with the same oil blend (0.007 ± 0.003 l per day) to meet the initial level. This replenishment method was adopted to replicate the same practices used in fried and fast food outlets [40]. At the end of the 10th day, viscous dark brown oil was obtained. To prevent photodegradation it was stored in amber color bottles and labeled as RHMVO.

Experimental animals

Healthy adult male rabbits of local strain weighing between 1450 ± 20 g were purchased from the animal house of Department of Pharmacology, University of Karachi, Pakistan. Rabbits were kept individually in wire-topped steel cages with a wooden bottom, provided control conditions of relative humidity (50–60%) and temperature (23 ± 2 °C) for 16 weeks with an estimated 12/12 h light/dark photo-cycle. Animals were acclimatized with the above-mentioned conditions for seven days before starting the experiments. Animals were handled according to the institutional animals’ ethical committee guidelines.

Experimental procedure

Doses were calculated based on grams per kg [42] and higher doses (double the normal) of oil were used to mimic the high intake with fried food. The daily recommended amount of edible vegetable oils for human adult males is 35–55 g per day (0.94 g/ml) [43]. The average body mass of an Asian male adult is around 57.7 kg [44]. On the basis of these facts normal daily dose of the oil is calculated to be 1 ml/kg/day. To imitate the higher intake of the oil with fried food, the dose of 2 ml/kg/day was calculated. Oil consumption, duration of 16 weeks was selected (equivalent to 12 years of human life). The study was performed by randomly allocating rabbits in the following treatment categories and the control group (n = 12).

  • Control group: Unexposed control rabbits

  • STHMVO group: animals were orally administered STHMVO (1 ml/kg/day)

  • L-RHMVO group: rabbits were orally administered RHMVO (1 ml/kg/day)

  • H-RHMVO group: rabbits were orally administered RHMVO (2 ml/kg/day)

Animals of all the groups had free access to water. The animals of study groups were administered respective oils in predefined doses, daily at 10 am through the oral route with the help of a syringe. For the rest of the day animals of all the groups were fed ad libitum on a regular diet (fresh hay and water). Control group animals were fed on fresh hay and water only. Morbidity and mortality were monitored. Animal’s body weight was recorded at baseline followed by weekly monitoring for 4 weeks, then on weeks 8, 12 and 16. At the completion of the study period (16 weeks) animals were euthanized through the intravenous administration of sodium pentobarbital 100 mg per kg followed by decapitation [45]. Furthermore, animals were necropsied for histopathological examination of internal organs and to retrieve the liver for organ weight evaluation. Food and water intake were recorded for each group.

Blood sample collection and liver function markers analysis

Blood was collected from the ear vein of animals in a fasting state after the completion of 16thweek. For hematological parameter study, 5 ml blood was collected in gel tubes for biochemical analysis. Blood was centrifuged at 3000 rpm for 15 min duration to isolate the serum. With the use of clean, dry disposable plastic syringes the serum was collected and stored at a temperature of − 20 °C and then used to analyze for total-protein, albumin, serum glutamic-pyruvic transaminase (SGPT), serum glutamic-oxaloacetic transaminase (SGOT) and alkaline phosphatase (ALP) using analytical kits of RANDOX Laboratories Ltd. following the manufacturer’s instructions.

Lipid peroxidation- malondialdehyde measurement

Lipid-peroxidation in tissue homogenate was evaluated as per the Wills method (1969). Absorbance was measured at 532 nm. Malondialdehyde (MDA) amount is expressed in nano-moles/gram of tissue wet-weight.

Hepatic antioxidant-enzymes activity measurement

To assay liver, homogenate activity of superoxide dismutase (SOD) Beyer and Fridovich method [46] was followed using spectrophotometric analysis. Inhibition of nitro blue tetrazolium (NBT) oxidation by SOD was measured. A unit of superoxide dismutase represented the SOD requirement to inhibit a 50% rate of NBT oxidation at 25 °C. Activity is shown in the unit per mg of protein. With slight changes in Euler’s method [47], the activity of catalase (CAT) was measured. The capacity of CAT to decompose hydrogen peroxide was measured at 240 nm. Used extinction-coefficient of 0.043 mM-1 cm-1. One unit of activity is defined as hydrogen peroxide degraded /minute/mg protein. Flohe and Gunzler method was followed for measurement of activity of glutathione peroxidase (GPx), articulated at 25 °C in mmol of GSH oxidized/minute per mg of protein.

Microscopic examination

After getting the weight of the liver, the tissue samples were treated with alcohol to dehydrate. After cleaning with xylene, samples were further embedded in paraffin at 56 °C, (melting point). By using rotatory microtome 5 μm sized sections were obtained. After flattening on warm water, they were mounted onto albumerised slides and keep for drying for 12 h. Dewaxing in xylene and hydration with ethanol and water was performed. The sections were first treated with Harris haematoxylin to stain, thereafter differentiation by acid alcohol then staining in methylene blue was performed. Furthermore, dehydration of sections in alcohol (95%) and staining in alcohol eosin (10%), dehydration with absolute alcohol and cleaning with xylene were completed. The sections were then mounted using Canada balsam. These prepared slides were finally viewed with the use of a light microscope.

Statistical analysis

In our study, the final data were accessible in the form of mean ± standard deviation, 95% CI and CV%. We applied analysis of variance (ANOVA) followed by post hoc Tukey’s Honest Significant Difference (HSD) test to find out statistical significance at p < 0.05. Statistical Product and Service Solutions software was used.

Results

Nutritional status and growth

Weight changes (body and liver) were observed in all the groups consistently for 16 weeks. As shown in (Table 1) statistically significant weight gain was observed at both high and low doses treated RHMVO despite lowered food and water intake (Fig. 1). In STHMVO treated group body and liver weight gain along with food and water intake was insignificantly different from control.

Table 1 Comparison of nutritional status and growth in rabbits from the control and different oils (STHMVO, L-RHMVO & H-RHMVO) fed groups at 16 weeks (n = 12)
Full size table
Fig. 1
figure1

Comparison of weight gain in rabbits from the control and different oils (STHMVO, L-RHMVO & H-RHMVO) fed groups at 16 weeks (n = 12)

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Biochemical markers of hepatic-function

Plasma level of hepatic-function markers; serum glutamic-pyruvic transaminase (SGPT), serum glutamic-oxaloacetic transaminase (SGOT), alkaline phosphatase (ALP) was increased, and level of albumin and total protein were significantly decreased (p < 0.05) in both low and high RHMVO fed groups in comparison with control and STHMVO fed group (Table 2). Insignificant changes were observed in the STHMVO group in comparison with control.

Table 2 Comparison of plasma liver-specific enzymes in rabbits from the control and different oils (STHMVO, L-RHMVO & H-RHMVO) fed groups at 16 weeks (n = 12)
Full size table

Antioxidant-enzymes and malondialdehyde level

Antioxidant enzymes like catalase (CAT), glutathione peroxidase (GPx), and superoxide dismutase (SOD) were significantly (P < 0.05) decreased in L-RHMVO and H-RHMVO groups in a dose-dependent manner in comparison with STHMVO and control (Table 3). In the analysis of lipid peroxidation in the organs showing lipidosis, along with significantly elevated malondialdehyde (MDA) levels in L-RHMVO and H-RHMVO groups. In microscopic findings of the liver, extensive lipid accumulation was observed in L-RHMVO and H-RHMVO group rabbits (Fig. 2).

Table 3 Comparison of hepatic-antioxidant enzyme and malondialdehyde levels in rabbits from the control and different oils (STHMVO, L-RHMVO & H-RHMVO) fed groups at 16 weeks (n = 12)
Full size table
Fig. 2
figure2

Histopathological images of rabbits liver after 16-week treatment: Control (a), Normal rabbit liver, STHMVO treated (b) observed an insignificant number of fibrous tissues in the portal area. L-RHMVO treated (c) fibrosis found around the portal area with fibrous septa forming in the lobule and H-RHMVO treated (d) a large number of fibrous septa formed. Which damaged the hepatic lobule (× 200)

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Discussion

Following long term oil treatment, the body and liver weight gain in RHMVO fed animals, both in high and low doses was statistically significant (p < 0.05) in comparison with control. In addition, the feeding-efficiency of RHMVO treated animals was lesser than STHMVO fed rabbits. That may be clarified as nearly all amino acids (AAs) react with oxidized lipids and their primary and secondary product, thus leading to decreased digestive utilization of AAs, proteins and fats, a contributing factor for weight gain [48]. The weight variances among the oil feed groups are in line with Sayon-Orea et al. study, which reported that fried edible products increased central adiposity and blood pressure [49]. Other evidence of increased risk of obesity, reduced HDL-cholesterol and bigger circumference of waist have been associated with the intake of food products, processed in repeatedly heated oil [49, 50]. The results of our study, with increased body and organ weight but comparatively reduced food intake in RHMVO fed animals are supported by other studies which reported the relationship between indigestibility and repeatedly heated oil consumption [51,52,53]. This increased body weight might be possibly linked with the deprived pancreatic lipase effect on triacylglycerol, polymers, dimers, and oligomers, present in thermally degenerated oils, as reported in a recent review [54].

The number of biochemical variables of biological-membranes and plasma is strongly influenced by dietary fat. Vegetable oils used in daily life exert their health effect through hepatic protection or damage, depending on factors like quantity used, FAs composition, heating duration, and extent [55, 56]. The results of the current study have shown that repeatedly heated oil-fed groups reported the maximum hepatic damage in a dose-dependent manner, even the intake of low doses may lead to liver toxicity. The results of our study are consistent with previous studies which reported significantly increased serum liver enzyme levels (including SGPT, SGOT, and ALP), which is clearly indicative of hepatic injury [57, 58]. The liver is clearly damaged by excessive free radical and may result in hepatitis, cirrhosis and hepatic tumor [19]. Thermally oxidized oil is the most significant source of oxidative damage for human health if used daily for a long time. In H-RHMVO groups, highly elevated levels of SGOT (sensitive and a precise biomarker for hepatotoxicity) and ALP (the main biomarker of hepatic and biliary defects like cholestasis) [59] reflected hepatocytes damage and tissue interruption, allowing the leakage of intracellular enzymes in the blood [55]. Consistent with the diminished serum albumin and total protein levels and supported by the significantly enlarged liver and histopathological changes in hepatocytes of RHMVO fed rabbits.

The results of hepatic-antioxidant enzyme levels suggest a strong indication of liver lipid-peroxidation with RHMVO intake both in high and low doses. The levels of MDA gauge the lipid peroxidation in the degradative phase. The MDA levels in H-RHMVO and L-RHMVO groups increased very significantly (p < 0.005) in comparison with the control group. Although the magnitude of the MDA level was dose-dependent, statistically not significantly different between the low and high dose RHMVO fed groups. Showing the deleterious effect of long-term RHMVO consumption, even in low doses. The finding of our study also confirms that with the consumption of single time heated mix vegetable oils, hepatic lipid-peroxidation was insignificant in comparison with control. Our study confirms that feeding on mixed oxidized oils provides a straight source of oxidative stress for the biological system. The composition of FAs is an important factor as biological membrane adapts, changes as per FAs provided in dietary fats [29, 60, 61], subsequently influence the cellular susceptibility to oxidative stress [57]. With the removal of OH• from a -CH2- group of polyunsaturated fatty acids, lipid peroxidation begins. Further conjugated dienes (CDs) are formed by molecular rearrangement. CDs contain 2 double bonds with a single bond as a separator. CDs react with oxygen to form peroxyl radicals, which further react with OH• atom from lipids and produce cyclic peroxides, lipid hydro-peroxides and MDA [29]. Lipid peroxidation in the biological membrane leads to impairment in the membrane functioning, structural integrity and reduced membrane fluidity with compromised enzyme activity present in the membrane [57]. The phospholipids of biological membrane holding trans-fatty acids attract cholesterol [58], leading to structural changes and functional alteration in the signaling mechanism, which further promotes the ROS production [62]. This phenomenon justifies the increased oxidative stress in RHMVO fed animals.

Comparative oxidative stress among all the groups was analyzed by antioxidant enzyme levels. Results show that significant (p < 0.05) reduction in SOD, GPx and lower CAT levels in H-RHMVO and L-RHMVO groups in comparison with control. Other South Asian region animal studies also support our results, but all these studies were conducted with single edible oil [42]. These results suggest that consumption of thermally oxidized oils may cause genotoxicity and carcinogenicity [63, 64]. As altered antioxidant activity further leads to oxygen intolerance, protein and DNA oxidation and finally cellular death [29]. In addition, antioxidant enzyme activity is inhibited by the toxic intermediates formed due to high-fat diet consumption [65] and accumulated H2O2 and oxygen-radicals also support the rapid formation of hydroxyl radicals [66]. This study emphasizes that the consumption of thermally oxidized mix vegetable oils is associated with a significantly reduced hepatic antioxidant-enzymatic system and induced hepatic-oxidative stress and pro-inflammatory state in rabbits. Further advance animal and human studies are required to evaluate the formation of DNA adducts with thermally oxidized oils in a model that mimics the human situation, considering the food processed in oxidized oils and roadside contamination being the part of the study design.

In normal routine consumers get exposed to several complex mixtures of substances and environmental chemicals so one-exposure-one-health-effect is not a realistic approach [67] but in a developing country like Pakistan, this study will provide information on real-life ground realities to divert attention towards these unaddressed issues. This study will also help to shift the paradigm to select the study models that mimic the human situation in developing societies.

Conclusion

In conclusion, this study highlighted that long-term consumption of oxidized mix edible oils induced hepatic-toxicity and lipid-peroxidation with induced oxidative stress in comparison with single time heated mixed vegetables oils. As the blend of oils was the same in single and multiple times heated oils mixture, so we conclude that trans-isomerization of fatty acids during thermal oxidation has the strongest association with hepatic oxidative stress rather than only the composition of fatty acids in the oil blend. This study also concludes that the consumption of thermally oxidized oils blend even in lower amounts is deleterious to health. This study provides strong evidence of hepatic dysfunction for lipid metabolism with a daily intake of low and high doses of thermally oxidized mixed vegetable oils, a key factor of the cardio-metabolic syndrome. This study highlights the knowledge, awareness of harmful health effects of eating food processed in RHMVO and also highlights the importance of conducting further animal and human studies in a model that mimics the real-life scenario in developing countries, to evaluate the reasons for increased incidences of CVDs and cancer in the South Asian region.

Availability of data and materials

All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ROS:

Reactive oxygen species

SGOT:

Serum glutamic-oxaloacetic transaminase

SGPT:

Serum glutamic pyruvic transaminase

ALP:

Alkaline phosphatase

SOD:

Superoxide dismutase

CAT:

Catalase

GPx:

Glutathione peroxidase

MDA:

Malondialdehyde

CDs:

Conjugated dienes

References

  1. 1.

    Vaskova H, Buckova M. Thermal degradation of vegetable oils: spectroscopic measurement and analysis. Procedia Eng. 2015;100:630–5.

    CAS  Article  Google Scholar 

  2. 2.

    Sommerfeld M. Trans unsaturated fatty acids in natural products and processed foods. Prog Lipid Res. 1983;22(3):221–33.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  3. 3.

    Andrikopoulos NK, Kalogeropoulos N, Falirea A, Barbagianni MN. Performance of virgin olive oil and vegetable shortening during domestic deep-frying and pan-frying of potatoes. Int J Food Sci Technol. 2002;37(2):177–90.

    CAS  Article  Google Scholar 

  4. 4.

    Owu D, Orie N, Osim E. Altered responses of isolated aortic smooth muscle following chronic ingestion of palm oil diets in rats. Afr J Med Med Sci. 1997;26:83–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Lopez-Garcia E, Schulze MB, Meigs JB, Manson JE, Rifai N, Stampfer MJ, et al. Consumption of trans fatty acids is related to plasma biomarkers of inflammation and endothelial dysfunction. J Nutr. 2005;135(3):562–6.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  6. 6.

    Adam SK, Das S, Soelaiman IN, Umar NA, Jaarin K. Consumption of repeatedly heated soy oil increases the serum parameters related to atherosclerosis in ovariectomized rats. Tohoku J Exp Med. 2008;215(3):219–26.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  7. 7.

    Adam SK, Soelaiman IN, Umar NA, Mokhtar N, Mohamed N, Jaarin K. Effects of repeatedly heated palm oil on serum lipid profile, lipid peroxidation and homocysteine levels in a post-menopausal rat model. McGill J Med. 2008;11(2):145.

    PubMed  PubMed Central  Google Scholar 

  8. 8.

    Leong XF, Aishah A, Aini UN, Das S, Jaarin K. Heated palm oil causes rise in blood pressure and cardiac changes in heart muscle in experimental rats. Arch Med Res. 2008;39(6):567–72.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  9. 9.

    Dung C-H, Wu S-C, Yen G-C. Genotoxicity and oxidative stress of the mutagenic compounds formed in fumes of heated soybean oil, sunflower oil and lard. Toxicol in Vitro. 2006;20(4):439–47.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  10. 10.

    Sinha R, Chow WH, Kulldorff M, Denobile J, Butler J, Garcia-Closas M, et al. Well-done, grilled red meat increases the risk of colorectal adenomas. Cancer Res. 1999;59(17):4320–4.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Sun Q, Ma J, Campos H, Hankinson SE, Manson JE, Stampfer MJ, et al. A prospective study of trans fatty acids in erythrocytes and risk of coronary heart disease. Circulation. 2007;115(14):1858–65.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  12. 12.

    Kinsella JE, Bruckner G, Mai J, Shimp J. Metabolism of trans fatty acids with emphasis on the effects of trans, trans-octadecadienoate on lipid composition, essential fatty acid, and prostaglandins: an overview. Am J Clin Nutr. 1981;34(10):2307–18.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  13. 13.

    Mozaffarian D, Rimm EB, King IB, Lawler RL, McDonald GB, Levy WC. Trans fatty acids and systemic inflammation in heart failure. Am J Clin Nutr. 2004;80(6):1521–5.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  14. 14.

    Harvey KA, Arnold T, Rasool T, Antalis C, Miller SJ, Siddiqui RA. Trans-fatty acids induce pro-inflammatory responses and endothelial cell dysfunction. Br J Nutr. 2008;99(4):723–31.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  15. 15.

    Lim SS, Gaziano TA, Gakidou E, Reddy KS, Farzadfar F, Lozano R, et al. Prevention of cardiovascular disease in high-risk individuals in low-income and middle-income countries: health effects and costs. Lancet. 2007;370(9604):2054–62.

    PubMed  Article  PubMed Central  Google Scholar 

  16. 16.

    Nishtar S. Prevention of coronary heart disease in South Asia. Lancet. 2002;360(9338):1015–8.

    PubMed  Article  PubMed Central  Google Scholar 

  17. 17.

    Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.

    PubMed  PubMed Central  Article  Google Scholar 

  18. 18.

    Tembhurne SV, Sakarkar DM. Anti-obesity and hypoglycemic effect of ethanolic extract of Murraya koenigii (L) leaves in high fatty diet rats. Asian Pac J Trop Dis. 2012;2:S166–S8.

    Article  Google Scholar 

  19. 19.

    Ilavenil S, Karthik D, Arasu MV, Vijayakumar M, Srigopalram S, Arokiyaraj S, et al. Hepatoprotective mechanism of lycorine against carbon tetrachloride induced toxicity in Swiss albino mice–a proteomic approach. Asian Pac J Reprod. 2015;4(2):123–8.

    Article  Google Scholar 

  20. 20.

    Shen B, Chen H, Shen C, Xu P, Li J, Shen G, et al. Hepatoprotective effects of lignans extract from Herpetospermum caudigerum against CCl4-induced acute liver injury in mice. J Ethnopharmacol. 2015;164:46–52.

    CAS  PubMed  Article  Google Scholar 

  21. 21.

    Fashir B, Sivasubramaniam V, Al Momen S, Assaf H. Pattern of liver disease in a Saudi patient population: a decade of experience at security forces hospital, Riyadh. KSA Saudi J Gastroenterol. 1996;2(1):50.

    CAS  PubMed  Google Scholar 

  22. 22.

    Abdel-Moneim AS, Bamaga MS, Shehab GM, Abu-Elsaad A-AS, Farahat FM. HCV infection among Saudi population: high prevalence of genotype 4 and increased viral clearance rate. PLoS One. 2012;7(1):e29781.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  23. 23.

    Obogwu MB, Akindele AJ, Adeyemi OO. Hepatoprotective and in vivo antioxidant activities of the hydroethanolic leaf extract of Mucuna pruriens (Fabaceae) in antitubercular drugs and alcohol models. Chin J Nat Med. 2014;12(4):273–83.

    CAS  PubMed  Google Scholar 

  24. 24.

    Obara N, Fukushima K, Ueno Y, Wakui Y, Kimura O, Tamai K, et al. Possible involvement and the mechanisms of excess trans-fatty acid consumption in severe NAFLD in mice. J Hepatol. 2010;53(2):326–34.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  25. 25.

    Maritim AC, Sanders RA, Watkins JB 3rd. Diabetes, oxidative stress, and antioxidants: a review. J Biochem Mol Toxicol. 2003;17(1):24–38.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  26. 26.

    Thannickal VJ, Fanburg BL. Reactive oxygen species in cell signaling. Am J Phys Lung Cell Mol Phys. 2000;279(6):L1005–L28.

    CAS  Google Scholar 

  27. 27.

    Lee J, Koo N, Min DB. Reactive oxygen species, aging, and antioxidative nutraceuticals. Compr Rev Food Sci Food Saf. 2004;3(1):21–33.

    CAS  Article  Google Scholar 

  28. 28.

    Halliwell B. Antioxidants and human disease: a general introduction. Nutr Rev. 1997;55(1):S44–S9.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  29. 29.

    Halliwell B, Gutteridge JM. Free radicals in biology and medicine. USA: Oxford University Press; 2015.

    Book  Google Scholar 

  30. 30.

    Ighodaro O, Akinloye O. First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): their fundamental role in the entire antioxidant defence grid. Alexandria J Med. 2018;54(4):287–93.

    Article  Google Scholar 

  31. 31.

    Nakai A, Oya A, Kobe H, Asakura H, Yokota A, Koshino T, et al. Changes in maternal lipid peroxidation levels and antioxidant enzymatic activities before and after delivery. J Nippon Med School. 2000;67(6):434–9.

    CAS  Article  Google Scholar 

  32. 32.

    Spiteller G. The important role of lipid peroxidation processes in aging and age dependent diseases. Mol Biotechnol. 2007;37(1):5–12.

    CAS  PubMed  Article  Google Scholar 

  33. 33.

    Ho E, Galougahi KK, Liu C-C, Bhindi R, Figtree GA. Biological markers of oxidative stress: applications to cardiovascular research and practice. Redox Biol. 2013;1(1):483–91.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  34. 34.

    Mapara M, Thomas BS, Bhat K. Rabbit as an animal model for experimental research. Dent Res J. 2012;9(1):111.

    Article  Google Scholar 

  35. 35.

    Fan J, Kitajima S, Watanabe T, Xu J, Zhang J, Liu E, et al. Rabbit models for the study of human atherosclerosis: from pathophysiological mechanisms to translational medicine. Pharmacol Ther. 2015;146:104–19.

    CAS  PubMed  Article  Google Scholar 

  36. 36.

    Lozano WM, Arias-Mutis OJ, Calvo CJ, Chorro FJ, Zarzoso M. Diet-induced rabbit models for the study of metabolic syndrome. Animals. 2019;9(7):463.

    Article  Google Scholar 

  37. 37.

    Safwat GM, Pisanò S, D'Amore E, Borioni G, Napolitano M, Kamal AA, et al. Induction of non-alcoholic fatty liver disease and insulin resistance by feeding a high-fat diet in rats: does coenzyme Q monomethyl ether have a modulatory effect? Nutrition. 2009;25(11–12):1157–68.

    CAS  PubMed  Article  Google Scholar 

  38. 38.

    Cano A, Ciaffoni F, Safwat GM, Aspichueta P, Ochoa B, Bravo E, et al. Hepatic VLDL assembly is disturbed in a rat model of nonalcoholic fatty liver disease: is there a role for dietary coenzyme Q? J Appl Physiol. 2009;107(3):707–17.

    CAS  PubMed  Article  Google Scholar 

  39. 39.

    Dhibi M, Brahmi F, Mnari A, Houas Z, Chargui I, Bchir L, et al. The intake of high fat diet with different trans fatty acid levels differentially induces oxidative stress and non alcoholic fatty liver disease (NAFLD) in rats. Nutr Metab. 2011;8(1):65.

    CAS  Article  Google Scholar 

  40. 40.

    Del Carmen F-ÁM, Molina-Hernández EF, Hernández-Raya JC, Sosa-Morales ME. The effect of food type (fish nuggets or French fries) on oil blend degradation during repeated frying. J Food Sci. 2012;77(11):C1136–C43.

    Article  CAS  Google Scholar 

  41. 41.

    Katragadda HR, Fullana A, Sidhu S, Carbonell-Barrachina ÁA. Emissions of volatile aldehydes from heated cooking oils. Food Chem. 2010;120(1):59–65.

    CAS  Article  Google Scholar 

  42. 42.

    Venkata RP, Subramanyam R. Evaluation of the deleterious health effects of consumption of repeatedly heated vegetable oil. Toxicol Rep. 2016;3:636–43.

    Article  CAS  Google Scholar 

  43. 43.

    Mozaffarian D, Ludwig DS. The 2015 US dietary guidelines: lifting the ban on total dietary fat. Jama. 2015;313(24):2421–2.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  44. 44.

    Walpole SC, Prieto-Merino D, Edwards P, Cleland J, Stevens G, Roberts I. The weight of nations: an estimation of adult human biomass. BMC Public Health. 2012;12(1):439.

    PubMed  PubMed Central  Article  Google Scholar 

  45. 45.

    Leary SL, Underwood W, Anthony R, Cartner S, Corey D, Grandin T, et al., Editors. AVMA guidelines for the euthanasia of animals: 2013 edition 2013: American Veterinary Medical Association Schaumburg.

  46. 46.

    Beyer WF Jr, Fridovich I. Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Anal Biochem. 1987;161(2):559–66.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  47. 47.

    Euler HV, Josephson K. Über katalase. I Justus Liebigs Annalen der Chemie. 1927;452(1):158–81.

    Article  Google Scholar 

  48. 48.

    López-Varela S, Sanchez-Muniz F, Cuesta C. Decreased food efficiency ratio, growth retardation and changes in liver fatty acid composition in rats consuming thermally oxidized and polymerized sunflower oil used for frying. Food Chem Toxicol. 1995;33(3):181–9.

    PubMed  Article  PubMed Central  Google Scholar 

  49. 49.

    Sayon-Orea C, Bes-Rastrollo M, Basterra-Gortari F, Beunza J, Guallar-Castillon P, De la Fuente-Arrillaga C, et al. Consumption of fried foods and weight gain in a Mediterranean cohort: the SUN project. Nutr Metab Cardiovasc Dis. 2013;23(2):144–50.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  50. 50.

    Guallar-Castillón P, Rodríguez-Artalejo F, Fornés NS, Banegas JR, Etxezarreta PA, Ardanaz E, et al. Intake of fried foods is associated with obesity in the cohort of Spanish adults from the European prospective investigation into Cancer and nutrition. Am J Clin Nutr. 2007;86(1):198–205.

    PubMed  Article  PubMed Central  Google Scholar 

  51. 51.

    Márquez-Ruiz G, Pérez-Camino M, Dobarganes M. Digestibility of fatty acid monomers, dimers and polymers in the rat. J Am Oil Chemists Soc. 1992;69(9):930–4.

    Article  Google Scholar 

  52. 52.

    Márquez-Ruiz G, Pérez-Camino M, Dobarganes M. Evaluation of hydrolysis and absorption of thermally oxidized olive oil in non-absorbed lipids in the rat. Ann Nutr Metab. 1993;37(3):121–8.

    PubMed  Article  PubMed Central  Google Scholar 

  53. 53.

    Olivero-David R, Paduano A, Fogliano V, Vitaglione P, Bastida S, González-Munoz MJ, et al. Effect of thermally oxidized oil and fasting status on the short-term digestibility of ketolinoleic acids and total oxidized fatty acids in rats. J Agric Food Chem. 2011;59(9):4684–91.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  54. 54.

    Dobarganes C, Márquez-Ruiz G. Possible adverse effects of frying with vegetable oils. Br J Nutr. 2015;113(S2):S49–57.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  55. 55.

    Quiles JL, Huertas JR, Battino M, Ramírez-Tortosa MC, Cassinello M, Mataix J, et al. The intake of fried virgin olive or sunflower oils differentially induces oxidative stress in rat liver microsomes. Br J Nutr. 2002;88(1):57–65.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  56. 56.

    Nakbi A, Tayeb W, Grissa A, Issaoui M, Dabbou S, Chargui I, et al. Effects of olive oil and its fractions on oxidative stress and the liver's fatty acid composition in 2, 4-Dichlorophenoxyacetic acid-treated rats. Nutr Metab. 2010;7(1):80.

    Article  CAS  Google Scholar 

  57. 57.

    Gutteridge JM, Halliwell B. Free radicals and antioxidants in the year 2000: a historical look to the future. Ann N Y Acad Sci. 2000;899(1):136–47.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  58. 58.

    Niu S-L, Mitchell DC, Litman BJ. Trans fatty acid derived phospholipids show increased membrane cholesterol and reduced receptor activation as compared to their cis analogs. Biochemistry. 2005;44(11):4458–65.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  59. 59.

    Schefer K, Hagen R, Ringer S, Schwarzwald C. Laboratory, electrocardiographic, and echocardiographic detection of myocardial damage and dysfunction in an Arabian mare with nutritional masseter myodegeneration. J Vet Intern Med. 2011;25(5):1171–80.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  60. 60.

    Yamaoka S, Urade R, Kito M. Mitochondrial function in rats is affected by modification of membrane phospholipids with dietary sardine oil. J Nutr. 1988;118(3):290–6.

    CAS  PubMed  Article  Google Scholar 

  61. 61.

    Charnock JS, McLennan PL, Abeywardena MY. Dietary modulation of lipid metabolism and mechanical performance of the heart. Mol Cell Biochem. 1992;116(1–2):19–25.

    CAS  PubMed  Article  Google Scholar 

  62. 62.

    Brown DA. Lipid rafts, detergent-resistant membranes, and raft targeting signals. Physiology. 2006;21(6):430–9.

    CAS  PubMed  Article  Google Scholar 

  63. 63.

    Srivastava S, Singh M, George J, Bhui K, Saxena AM, Shukla Y. Genotoxic and carcinogenic risks associated with the dietary consumption of repeatedly heated coconut oil. Br J Nutr. 2010;104(9):1343–52.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  64. 64.

    Srivastava S, Singh M, George J, Bhui K, Shukla Y. Genotoxic and carcinogenic risks associated with the consumption of repeatedly boiled sunflower oil. J Agric Food Chem. 2010;58(20):11179–86.

    CAS  PubMed  Article  Google Scholar 

  65. 65.

    Thampi B, Manoj G, Leelamma S, Menon V. Dietary fiber and lipid peroxidation: effect of dietary fiber on levels of lipids and lipid peroxides in high fat diet. Indian J Exp Biol. 1991;29(6):563–7.

    CAS  PubMed  Google Scholar 

  66. 66.

    Batra S, Singh S, Srivastava V, Chatterjee R. Xanthine oxidase, superoxide dismutase, catalase and lipid peroxidation in Mastomys natalensis: effect of Dipetalonema viteae infection. Indian J Exp Biol. 1989;27(12):1067–70.

    CAS  PubMed  Google Scholar 

  67. 67.

    Docea A, Calina D, Goumenou M, Neagu M, Gofita E, Tsatsakis A. Study design for the determination of toxicity from long-term-low-dose exposure to complex mixtures of pesticides, food additives and lifestyle products. Toxicol Lett. 2016;258:S179.

    Article  Google Scholar 

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Acknowledgments

We acknowledge the kind support of Abdul Moiz Hussain and Dr. Junaid Iqbal for providing technical support in the process of final submission and language review.

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Affiliations

  1. Department of Pharmacy, Aga Khan University Hospital, Stadium Road (Main Pharmacy), P.O Box 3500, Karachi, 74800, Pakistan

    Gul Ambreen & Kashif Hussain

  2. Department of Pharmacology, University of Karachi, Karachi, Pakistan

    Afshan Siddiq

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  1. Gul Ambreen
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Contributions

1. GA: Substantial contributions to the conception or design of the work. Performed the study and wrote the paper, Analysis or interpretation of data. 2. AS: Revised the work critically for important intellectual content. Supervised the research, Final approval of the version published. 3. KH: Co-wrote the paper and final review of the manuscript. All the authors read and approved the final manuscript before submission.

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Correspondence to Gul Ambreen.

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Ethics approval and consent to participate

Research study protocol along with the procedures to be followed during our research study, euthanasia and ethical authorization of the study all got approved from the Board of Advanced Studies & Research (BASR) of the University of Karachi (BASR number:03296/Pharm).

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The authors declare that they have no competing interests” in this section.

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Ambreen, G., Siddiq, A. & Hussain, K. Association of long-term consumption of repeatedly heated mix vegetable oils in different doses and hepatic toxicity through fat accumulation. Lipids Health Dis 19, 69 (2020). https://doi.org/10.1186/s12944-020-01256-0

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Keywords

  • Hepatic toxicity
  • Oxidative stress
  • RHMVO
  • STHMVO
  • Repeatedly heated mix vegetable oils

Lipids in Health and Disease

ISSN: 1476-511X