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Clinical Phytoscience

International Journal of Phytomedicine and Phytotherapy

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Effects of aqueous leaf extract of avocado (Persea americana) on total cholesterol, triacylglycerols, protein and haematological parameters in CCl4-intoxicated rats

Clinical Phytoscience volume 6, Article number: 14 (2020) Cite this article

Abstract

Background

Avocado (Persea americana) is one of the plants widely used in ethnomedicine in Nigeria. The present study was aimed at investigating effects of aqueous Avocado (Persea americana) leaf extract on total cholesterol, triacylglycerols, protein and haematological parameters in carbon tetrachloride (CCl4)-intoxicated rats.

Methods

We evaluated the possible effects of pre-treatment with aqueous extract of Persea americana (AEPA) on protein, total cholesterol (T-CHOL), triacylglycerols (TAGs) and haematological parameters in Wistar male albino rats intoxicated with CCl4. Group 1 was the healthy control; group 2 rats were pre-treated with Reducdyn® (100 mg/kg/day) as a standard drug, groups 4 and 5 rats were pre-treated with AEPA at a dose of 100 mg/kg and 200 mg/kg per day respectively, the treatments were administered orally for 7 days. On the seventh day, rats in the treatment groups were injected with a fresh mixture of CCl4 and olive oil (3 ml/kg, 1:1; sc).

Results

Pre-treatment of rats with AEPA resulted in marked increase (p < 0.05) in total protein and reduction in T-CHOL (19–34%) compared to CCl4 alone. Also, there was significant decrease (p < 0.05) in serum TAG concentration when rats were pre-treated with 100 mg and 200 mg kg− 1 b. wt. AEPA. Similarly, AEPA provoked (p < 0.05) a lowering of T-CHOL and TAG levels and an increase in liver protein concentration in the rats. Administration of AEPA at both concentrations restored (p < 0.05) WBC count and ameliorated neutropenia and lymphocytosis caused by CCl4 intoxication.

Conclusion

These results suggest that AEPA could be protective against the development of fatty liver and might also be exhibiting the potential to prevent alterations in haematological parameters caused by CCl4 intoxication in rats.

Introduction

The liver plays a pivotal role in drug and xenobiotic metabolism and is thus susceptible to attacks by these agents leading to liver injuries or damage. Injury to the liver results in several disorders including elevation in hepatic enzymes, steatosis (accumulation of triacylglycerols in the liver), reduced β-oxidation of fatty acids, and necrosis [7].

Fatty degeneration of the liver (steatosis) resulting from CCl4 intoxication is attributed to an imbalance between lipid biosynthesis and degradation. It could also result from the failure of triacylglycerols to be transferred as VLDL from liver to the circulation [7, 38].

In the rats, a major metabolic defect induced by CCl4 intoxication appears to be inhibition of triacylglycerols release from the liver. This inhibition of outward transport would allow the accumulation of triacylglycerols within the liver and the development of fatty liver associated with CCl4 poisoning [16].

Plant-derived drugs and herbal formulations are obtained from natural sources and their use have been on the increase in many countries around the world. This is because they are usually viewed to be less toxic and free from serious side effects than the conventional synthetic drugs [4, 6, 24].

Avocado (Persea americana) is one of the plants that have been widely used in ethno-medicine. In Nigeria, the leaf has various local names such as Ewé pia (Yoruba), Akwukwo Ube oyibo (Igbo), and Ganyen piya (Hausa).

Avocado leaves extracts have been reported to possess anti-inflammatory, antihypertensive/hypotensive, and hypoglycemic activities as well as vasorelaxant action and anticonvulsant effect [2, 3, 5, 14, 15, 26, 28]. Also, the leaf extracts of P. americana have been shown to be protective against cholesterol-induced hyperlipidemia in rats [9, 19].

The most abundant bioactive phytoconstituents of Avocado include phenolics, phytosterols, minerals, vitamins, and carotenoids [12, 27, 33]. These bioactive compounds have been shown to possess lipid-lowering, antidiabetic, cardioprotective, antiatherosclerotic activity [35].

Thus, the possible effects of aqueous AEPA on protein, total cholesterol (T-CHOL), triacylglycerols (TAGs) and haematological parameters in Wistar male albino rats intoxicated with carbon CCl4 were evaluated.

Materials and methods

Plant material

Fresh avocado leaves were collected from a cultivated plant in Ilupeju, Lagos. The leaves were authenticated at the Department of Botany, University of Lagos, and a voucher specimen (LUH 4199), was deposited at the herbarium of the department.

Preparation of plant extract

The leaves were air-dried, pulverized and the aqueous extract was prepared by loading the powdered leaves into a Soxhlet apparatus. The extraction lasted for 12 h, and the extract solution was evaporated to dryness in a rotary evaporator at 40 °C to obtain a residue labeled AEPA which was stored in clean vials until required.

Experimental animals

Thirty male Wistar strain albino rats (130–160 g), were purchased from the Animal House of Nigerian Institute of Medical Research (NIMR), Lagos. The rats were acclimatized for 1 week. and maintained under standard conditions of temperature (23 ± 2 °C) and 12 h light/dark cycle. The rats were treated with humane care, fed with a standard diet and water ad libitum.

Experimental design

Hepatoxicity was induced in the rats by subcutaneous injection of carbon tetrachloride as described by Wang et al. [37].

The albino rats were randomly divided into five treatment groups of six rats per group. Group 1served as healthy control. Groups 2, 3, 4, and 5 served as treatment groups. Group 2 rats received distilled water (3 ml/kg), Group 3 rats were pre-treated with Reducdyn® (100 mg/kg/day). Groups 4 and 5 rats were pre-treated with AEPA at a dose of 100 mg/kg and 200 mg/kg per day respectively. All the treatments were administered orally for 7 days. On the seventh day, rats in the treatment groups were subcutaneously injected with a fresh mixture of CCl4 and olive oil (3 ml/kg, 1:1), 30 minutes after the administration of the last dose of the pre-treatment drug (Group 3), or extract Groups 4 and 5), or distilled water (Group 2). Rats in Group 1 were administered olive oil (3 ml/kg, sc). After 24 h, the rats were sacrificed by cervical dislocation and blood samples collected by cardiac puncture into plain sterile tubes, allowed to coagulate and then centrifuged at 3000 rpm for 10 min., at 4 °C. The serum obtained was stored at -80 °C pending analysis. Some of the blood samples were also dispensed into clean ethylene diamine tetra acetic acid (EDTA)-containing bottles for haematological investigation. Rat livers were quickly excised and perfused with chilled 1.15% (w/v) potassium chloride (KCl) solution to remove all traces of haemoglobin. The livers were blotted dry, weighed and used to prepare liver homogenates.

Biochemical analysis

Protein concentration was determined using the Bradford method which is based on the absorbance maximum of Coomassie Brilliant Blue G-250 at 595 nm.

Total cholesterol (T-CHOL) and triacyglycerols (TAG), were measured using kits purchased from RANDOX Laboratories Ltd. (Crumlin, UK).

Haematological parameters

Haematological parameters including packed cell volume, hemoglobin concentration, white blood cell count, red blood cell count, eosinophils, lymphocyte and neutrophils counts, were measured using standard methods as described by Dacie and Lewis [10].

Statistical analysis

Results were expressed as mean ± standard error of the mean (S.E.M). Differences between the groups were determined using one-way analysis of variance (ANOVA). Statistical significance of the difference of means was determined and indicated by p-values ≤0.05.

Results

Effect of pre-treatment with aqueous leaf extract of P. americana on serum total protein, total cholesterol and triacylglycerols in CCl4 -induced hepatotoxicity in rats

Serum total cholesterol, triacylglycerols and protein concentrations in rats pre-treated with AEPA and challenged with CCl4 are as presented in Table 1. Serum T-CHOL level was slightly raised (12%) in CCl4-intoxicated rats compared to normal control rats. Pre-treatment with 100 mg and 200 mg kg− 1 b. wt. AEPA resulted in the lowering of T-CHOL by 19% and 34% respectively while pre-treatment with 100 mg kg− 1 b. wt. Reducdyn® caused 52% decrease in T-CHOL. Serum TAG concentration was markedly raised (p < 0.05; 113%) in CCl4-treated rats compared with healthy control. A significant reduction (p < 0.05; 65% and 64% of CCl4 control) in TAG concentration was observed when rats were pre-treated with 100 mg and 200 mg kg− 1 b. wt. AEPA, respectively. Serum total protein concentration was significantly reduced (p < 0.05; 54%) in CCl4-treated rats. Pre-treatment with 100 mg and 200 mg kg− 1 b. wt. AEPA caused a significant increase (p < 0.05; 119% and 129%, respectively) in serum protein compared to CCl4 control animals. However, the levels of T-CHOL, TAGs and protein in rats pre-treated with AEPA were not significantly different from the normal control.

Table 1 Effect of pre-treatment with aqueous leaf extract of P. americana on serum total protein, total cholesterol and triacylglycerols in CCl4 -induced hepatotoxicity in rats
Full size table

Effect of pre-treatment with aqueous leaf extract of P. americana on liver total protein, total cholesterol and triacylglycerols in CCl4-induced hepatotoxicity in rats

Liver protein, total cholesterol and triacylglycerol concentrations in CCl4-intoxicated rats and AEPA pre–treated rats are depicted in Table 2. Total cholesterol increased significantly (p < 0.05; 206%) in CCl4 control rats compared with healthy control. Pre-treatment with AEPA (100 mg and 200 mg kg− 1 b. wt.) significantly reduced (p < 0.05; 57% and 58% respectively) T-CHOL concentration compared to CCl4 control. Liver TAG concentration was profoundly elevated (p < 0.05; 351%) by CCl4 administration compared to healthy control. Pre-treatment with 100 mg and 200 mg kg− 1 b. wt. AEPA provoked a reduction in liver TAG (50% and 51% respectively) compared to CCl4. Total protein concentration was lowered by 18% following CCl4 intoxication and this was improved by pre-treatment with AEPA and Reducdyn® up to 14% and 18% respectively. There was no significant difference (p > 0.05) in the observed protection by AEPA and Redcdyn®.

Table 2 Effect of pre-treatment with aqueous leaf extract of P. americana on liver total protein, total cholesterol and triacylglycerols in CCl4-induced hepatotoxicity in rats
Full size table

Effect of pre-treatment with aqueous leaf extract of P. americana on peripheral blood smears in CCl4- intoxicated rats

Table 3 shows the levels of some haematological parameters observed in the experimental rats pre-treated with AEPA and intoxicated with CCl4. There was a non-significant decrease (p > 0.05) in the packed cell volume (7%) and haemoglobin concentration (7%) of CCl4-treated rats, respectively compared to healthy control. Also, total white blood cells (WBC) counts and neutrophils were significantly reduced (p < 0.05) while lymphocytes were increased by CCl4 administration compared to healthy control. Pre-treatment with 100 mg and 200 mg kg− 1 b. wt. AEPA restored WBC counts while pre-treatment with 100 mg kg− 1 b. wt. AEPA only increased neutrophils and lowered lymphocytes counts. Similarly, AEPA at 200 mg kg− 1 b. wt reduced packed cell volume and haemoglobin concentration by 12.5 and 19%, respectively.

Table 3 Effect of pre-treatment with aqueous leaf extract of P. americana on peripheral blood smears in CCl4- intoxicated rats
Full size table

Discussion

Administration of CCl4 caused inhibition of protein synthesis manifested as decrease in both serum and liver total proteins compared with healthy control. This finding is similar to earlier reports by other workers [1, 22, 23, 36]. Inhibition of protein synthesis in the liver is primarily considered to bring about lowering of lipoprotein synthesis and accumulation of fat in the liver, resulting in the development of fatty liver [30]. It is also suggested that a decline in total protein content is a useful index of the severity of cellular dysfunction in chronic liver diseases [36]. Pre-treatment with AEPA restored serum and liver total protein to near the levels in healthy controls. The restoration of total protein content in serum and liver of rats treated with AEPA is indicative of stimulation of protein synthesis. This could accelerate the regeneration process and the production of liver cells as well as further elucidate its hepatoprotective activity.

Increases in the levels of cholesterol and TAGs were observed in serum and hepatic tissues. This confirms previous reports that CCl4 treatment provokes increase in cholesterol and TAGs levels in rat liver [18, 34, 36]. CCl4 increases the synthesis of fatty acids and TAGs from acetate. This could be due to the transport of acetate into the liver cell, resulting in increased substrate availability.

Also, it is postulated that the major metabolic defect induced by CCl4 intoxication to rats is inhibition of hepatic TAGs release. This inhibition of outward transport allows the accumulation of TAGs within the liver and the occurrence of fatty liver associated with CCl4 poisoning [16]. Intoxication with CCl4 has also been shown to increase the synthesis of cholesterol [7].

On the other hand, CCl4 reduces the hydrolysis of TAGs and ß-oxidation of fatty acids thus, making more fatty acids available for esterification [20]. Disruption of β-oxidation of fatty acids in the mitochondrial causes microvesicular steatosis, typified by accumulation of tiny lipid vesicles in the cytoplasm of hepatocytes [13]. Owing to reduced mitochondrial oxidation, non-esterified fatty acids (NEFAs) build up in the liver and become esterified into TAG. Also, it has been shown that during CCl4 toxicity, fat from the peripheral adipose tissue is translocated to the liver and kidney leading to its accumulation [11]. It is suggested that an essential step in the outward transport of hepatic TAGs is the synthesis of lipoproteins at the endoplasmic reticulum by the utilization of TAG previously synthesized at another site. Damage to the endoplasmic reticulum during CCl4 intoxication inhibits lipoprotein synthesis. This may effectively decrease outward TAGs transport and results in the development of a fatty liver [16, 17, 29, 32]. These factors could possibly explain the significant increase in hepatic TAGs observed in CCl4-intoxicated rats in this study. However, pre-treatment with AEPA produced a substantial reduction in the elevated hepatic cholesterol and TAGs levels. This suggests that the extract prevented CCl4-induced hyperlipidaemia probably due to its hepatoprotective activity [8] in a mechanism that involves increase outward translocation of TAGs. P. americana has previously be shown to protect rats against cholesterol-induced hyperlipidemia by lowering total cholesterol, triglycerides and LDL, and increasing HDL levels [9, 19]. Various mechanisms have been postulated for the antihypertriglyceridemic activity of medicinal plants including: inhibition of sterol regulatory element-binding transcription factor 1 (SREBP-1), antioxidant and anti-inflammatory activities, inhibition of 3-hydroxy-3-methylglutaryl coenzyme A (HMGCoA) reductase, inhibition of lipogenesis, inhibition of leptin secretion among others [25, 31].

Administration of CCl4 alone caused leucopenia, neutropenia and lymphocytosis in the rats similar to the findings of Mandal et al. [21]. The administration of AEPA at a concentration of 100 mg and 200 mg kg− 1 b. wt restored WBC count level by 99% and 85% respectively compared to CCl4 control rats. This finding therefore suggests that AEPA has the potential to restore CCl4-induced alterations of haematological parameters in rats.

Conclusion

The increases in cholesterol and triacylglycerol provoked by CCl4 administration were considerably reduced by pre-treatment with AEPA. This suggests that AEPA could prevent CCl4-induced hyperlipidaemia and inhibit the development of fatty liver in the rats. Furthermore, AEPA exhibited the potential to prevent CCl4-induced leucopenia, lymphocytosis and other hematological related alterations in rats.

Availability of data and materials

Research data and materials can be provided on request.

Abbreviations

AEPA:

Aqueous extract of Persia americana

B:

Basophils (%)

CCl4 :

Carbon tetrachloride

E:

Eosinophils (%)

Hb:

Haemoglobin (g/dl)

L:

Lymphocytes (%)

M:

Monocytes (%)

N:

Neutrophils (%)

PCV:

Packed cell volume (%)

TAG:

Triacylglycerol

T-CHOL:

Total cholesterol

WBC:

White blood cells (103/μL

References

  1. Abdel-Hamid NM. Diphenyl dimethyl Bicarboxylate as an effective treatment for chemical-induced fatty liver in rats. Afr J Biomed Res. 2006;9:77–81.

    Google Scholar 

  2. Adeboye JO, Fajonyomi MO, Makinde JM, Taiwo OB. A preliminary study on the hypotensive activity of Persea americana leaf extracts in anaesthetized normontensive rats. Fitoterepia. 1999;70:15–20.

    Article  Google Scholar 

  3. Adeyemi OO, Okpo SO, Ogunti OO. Analgesic and anti-inflammatory effects of aqueous extract of leaves of Persea americana mill. (Lauraceae). Fitoterapia. 2002;73:375–80.

    Article  CAS  Google Scholar 

  4. Annapurna A, Mahalakshmi D, Murali K. Antidiabetic activity of a polyherbal preparation (tincture of punchparna) in normal and diabetic rats. Indian J Exp Biol. 2001;39:500–2.

    CAS  PubMed  Google Scholar 

  5. Antia BS, Okokon JE, Okon PA. Hypoglycemic activity of aqueous leaf extract of Persea americana mill. Indian J Pharmacol. 2005;37:325–6.

    Article  Google Scholar 

  6. Bhattacharya SK, Satyan KS, Chakrbarti A. Effect of Trasina, an Ayurvedic herbal formulation, on pancreatic islet superoxide dismutase activity in hyperglycemic rats. Indian J Exp Biol. 1997;35:297–9.

    CAS  PubMed  Google Scholar 

  7. Boll M, Weber LWD, Becker E, Stampfl A. Pathogenesis of carbon tetrachloride-induced hepatocyte injury. Bioactivation of CCl4 by cytochrome P450 and effect on lipid homeostasis. Z Naturforsch. 2001;56c:111–21.

    Article  Google Scholar 

  8. Brai BIC, Adisa RA, Odetola AA. Hepatoprotective properties of aqueous leaf extracts of Persea americana. Mill (Lauraceae) avocado against CCl4-induced damage in rats. Afr J Tradit Complement Altern Med. 2014;11(2):237–44.

    Article  Google Scholar 

  9. Brai BIC, Odetola AA, Agomo PU. Hypoglycemic and Hypocholesterolemic potential of Persea americana leaf extracts. J Med Food. 2007;10(2):356–60.

    Article  Google Scholar 

  10. Dacie JV, Lewis SM. Practical haematology 8th ed. London: Churchill Livingstone; 1995. p. 37–85.

  11. Devarshi P, Kanase A, Kanase R, Mane S, Patil S, Varute AT. Effect of mandur bhasma on lipolytic activities of liver, kidney and adipose tissue of albino rat during CCl4-induced hepatic injury. J Biosci. 1986;10:227–34.

    Article  Google Scholar 

  12. Dreher ML, Davenport AJ. Hass avocado composition and potential health effects. Crit Rev Food Sci Nutr. 2013;53:738–50.

    Article  CAS  Google Scholar 

  13. Fromenty B, Pessayre D. Inhibition of mitochondrial β-oxidation as a mechanism of hepatotoxicity. Pharmacol Ther. 1995;67:101–54.

    Article  CAS  Google Scholar 

  14. Girow LM, Freire V, Alonzo A, Caceres A. Ethnobotanical survey of the medicinal flora used by the Caribs of Guatemala. J Ethnopharmacol. 1991;34:143–87.

    Google Scholar 

  15. Guevarra AP, Espino MP, Chua C, Russel G. Anti-inflammatory principles of the leaves of Persea americana. Mill. Philipp J Sci. 1998;127:81–91.

    CAS  Google Scholar 

  16. Heimberg M, Weinstein I, Dishmon G, Dunkerley A. The action of carbon tetrachloride on the transport and metabolism of triglycerides and fatty acids by the isolated perfused rat liver and its relationship to the etiology of fatty liver. J Biol Chem. 1962;237:3623–7.

    CAS  Google Scholar 

  17. Honma T, Suda M. Changes in plasma lipo-proteins as toxicity markers for carbon tetrachloride, chloroform and dichloromethane. Ind Health. 1997;35:519–31.

    Article  CAS  Google Scholar 

  18. Kamalakkannan N, Rukkumani R, Viswanathan P, Rajasekharan KN, Menon VP. Effect of Curcumin and its analogue on lipids in carbon tetrachloride-induced hepatotoxicity: a comparative study. Pharm Biol. 2005;43:460–6.

    Article  CAS  Google Scholar 

  19. Kolawole OT, Kolawole SO, Adekunle AA, Olaniran IO. Methanol leaf extract of Persea americana protects rats against cholesterol-induced hyperlipidemia. Br J Med Med Res. 2012;2(2):235–42.

    Article  Google Scholar 

  20. Lieber CS. Alcoholic liver disease: new insights on pathogenesis lead to new treatment. J Hepatol. 2000;32:113–28.

    Article  CAS  Google Scholar 

  21. Mandal A, Karmakar R, Bandyopadhyay S, Chatterjee M. Antihepatotoxic potential of Trianthema portulacastrum in carbon tetrachloride-induced chronic hepatocellular injury in mice: reflection in haematological, histological and biochemical characteristics. Arch Pharm Res. 1998;21:223. https://doi.org/10.1007/BF02975279.

    Article  CAS  PubMed  Google Scholar 

  22. Manjunatha BK. Hepatoprotective activity of Pterocarpus santalinus L. f., an endangered medicinal plant. Indian J Pharmacol. 2006;38:25–8.

    Article  Google Scholar 

  23. Mankani KL, Krishna V, Manjunatha BK, Vidya SM, Jagadeesh Singh SD, Manohara YN, Raheman A, Avinash KR. Evaluation of hepatoprotective activity of stem bark of Pterocarpus marsupium Roxb. Indian J Pharmacol. 2005;37:165–8.

    Article  Google Scholar 

  24. Mitra SK, Gopumadhavan S, Muralidhar TS, Anturlika SD, Sujatha MB. Effect of a herbomineral preparation D-400 in streptozotocin induced diabetic rats. J Ethnopharmacol. 1996;54:41–6.

    Article  CAS  Google Scholar 

  25. Mollazadeh H, Mahdian D, Hosseinzadeh H. Medicinal plants in treatment of hypertriglyceridemia: a review based on their mechanisms and effectiveness. Phytomedicine. 2019;53:43–52.

    Article  CAS  Google Scholar 

  26. Ojewole JAO, Amabeoku GJ. Anticonvulsant effect of Persea americana mill (Lauraceae) (avocado) leaf aqueous extract in mice. Phytother Res. 2006;20:696–700.

    Article  Google Scholar 

  27. Owolabi MA, Coker HAB, Jaja SI. Bioactivity of the phytoconstituents of the leaves of Persea americana. J Med Plant Res. 2010;4(12):1130–5.

    CAS  Google Scholar 

  28. Owolabi MA, Jaja SI, Coker HAB. Vasorelaxant action of aqueous extract of the leaves of Persea americana on isolated thoracic rat aorta. Fitoterapia. 2005;76:567–73.

    Article  Google Scholar 

  29. Pencil D, Brattin WJ Jr, Glende EA Jr, Recknagel RO. Carbon tetrachloride-dependent inhibition of lipid secretion by isolated hepatocytes: characterization and requirement for bioactivation. Biochem Pharmacol. 1984;33:2419–23.

    Article  CAS  Google Scholar 

  30. Piriou A, Warnet JM, Jacqueson A, Claude JR, Truhaut R. Fatty liver induced by high doses of rifampicin in the rat: possible relation with an inhibition of RNA polymerases in eukaryotic cells. Arch Toxicol Suppl. 1979;2:333–7.

    Article  Google Scholar 

  31. Purit PE, Mangisah L, Suthama N. The effects of dietary supplementation of onion and garlic husk powder on protein, cholesterol, and fat of duck meat. In: Proceedings of International seminar on Livestock Production and Veterinary Technology. LPVT-2016; 2017. p. 422–7.

    Google Scholar 

  32. Recknagel RO, Lombardi B, Schotz MC. A new insight into the pathogenesis of carbon tetrachloride fat infiltration. Proc Soc Exp Biol Med. 1960;104:608–10.

    Article  CAS  Google Scholar 

  33. Rodriguez-Carpena JG, Morcuende D, Estevez M. Avocado by-products as inhibitors of color deterioration and lipid and protein oxidation in raw porcine patties subjected to chilled storage. Meat Sci. 2011;89:166–73.

    Article  CAS  Google Scholar 

  34. Seakins A, Robinson DS. The effect of administration of carbon tetrachloride on the formation of plasma lipoproteins in the rat. Biochem J. 1963;86:401–7.

    Article  CAS  Google Scholar 

  35. Tabeshpour J, Razavi BM, Hosseinzadeh H. Effect of avocado Persea americana on metabolic syndrome: a comprehensive systematic review. Phytother Res. 2017;31:819–37.

    Article  Google Scholar 

  36. Venukumar MR, Latha MS. Hepatoprotective effect of the Methanolic extract of Curculigo orchioides in CCl4 -treated male rats. Indian J Pharmacol. 2002;34:269–75.

    Google Scholar 

  37. Wang BJ, Liu CT, Tseng CY, Wu CP, Yu ZR. Hepatoprotective and antioxidant effects of Bupleurum kaoi Liu (Chao et Chuang) extract and its fractions fractionated using supercritical CO2 on CCl4-induced liver damage. Food Chem. Toxicol. 2004;42:609–17.

    Article  CAS  Google Scholar 

  38. Weber LWD, Boll M, Stampfl A. Hepatotoxicity and mechanism of action of haloalkanes: carbon tetrachloride as a toxicological model. Crit Rev Toxicol. 2003;33:105–36.

    Article  CAS  Google Scholar 

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This is a self-sponsored research project, no funding whatsoever was received.

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Authors and Affiliations

  1. Department of Biochemistry, Phytomedicine, Biochemical Pharmacology and Toxicology Unit, Federal University, Oye, Ekiti, Nigeria

    B. I. C. Brai & J. A. Falode

  2. Department of Biochemistry, College of Medicine, Laboratories for Biomembrane and Cancer Research, University of Lagos, Lagos, Nigeria

    R. A. Adisa

  3. Department of Biochemistry, University of Ibadan, Ibadan, Nigeria

    A. A. Odetola

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BBIC conceived, designed and carried out the laboratory experiments, wrote the manuscript; ARA read and improved the manuscript; FJA read and prepared the manuscript for publication; OAA designed and supervised the work.

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Brai, B.I.C., Falode, J.A., Adisa, R.A. et al. Effects of aqueous leaf extract of avocado (Persea americana) on total cholesterol, triacylglycerols, protein and haematological parameters in CCl4-intoxicated rats. Clin Phytosci 6, 14 (2020). https://doi.org/10.1186/s40816-020-00159-y

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