Global aflatoxin contamination of agricultural commodities is of the most concern in food safety and quality. This study investigated the hepatoprotective effect of 80% methanolic leaf extract of Annona senegalensis against aflatoxin B1 (AFB1)-induced toxicity in rats. A. senegalensis has shown to inhibit genotoxicity of aflatoxin B1in vitro. The rats were divided into six groups including untreated control, aflatoxin B1 only (negative control); curcumin (positive control; 10 mg/kg); and three groups receiving different doses (100 mg/kg, 200 mg/kg, and 300 mg/kg) of A. senegalensis extract. The rats received treatment (with the exception of untreated group) for 7 days prior to intoxication with aflatoxin B1. Serum levels of aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, lactate dehydrogenase, and creatinine were measured. Hepatic tissues were analysed for histological alterations. Administration of A. senegalensis extract demonstrated hepatoprotective effects against aflatoxin B1-induced toxicity in vivo by significantly reducing the level of serum aspartate aminotransferase and alanine aminotransferase and regenerating the hepatocytes. No significant changes were observed in the levels of alkaline phosphatase, lactate dehydrogenase, and creatinine for the AFB1 intoxicated group, curcumin+AFB1 and Annona senegalensis leaf extract (ASLE)+AFB1 (100 mg/kg, 200 mg/kg, and 300 mg/kg body weight [b.w.]) treated groups. Annona senegalensis is a good candidate for hepatoprotective agents and thus its use in traditional medicine may at least in part be justified.
Contribution
The plant extract investigated in this study can be used in animal health to protect the organism from toxicity caused by mycotoxins.
aflatoxin B1toxicityhepatoprotective activitySprague-Dawley ratsAnnona senegalensisFunding information The study was supported by the National Research Foundation (grant number CPRR 87746 and NRF/FWO 87964), Fonds Wetenschappelijk Onderzoek (FWO) grant number G001014N, Flemish Interuniversity Council (VLIR) under grant (ZEIN2014Z184) and the Agricultural Research Council.Introduction
Contamination of agricultural commodities with spoilage fungi and their mycotoxins is a prominent worldwide public health and food safety concerns (Fernandes et al. 2021). Food and feed are the most exposed agricultural commodities that are vulnerable to fungal contamination in different areas. This contamination also exposes humans and animals to different dietary mutagens on a daily basis (Medalcho et al. 2023). Some of these toxigenic fungi produce genotoxic and mutagenic secondary metabolites. Aflatoxin B1 (AFB1) is one of the most common dietary mutagenic, genotoxic, carcinogenic, immunosuppressive, and teratogenic metabolites produced by Aspergillus flavus and Aspergillus parasiticus (Medalcho et al. 2023; Zarev et al. 2020). It contaminates agricultural commodities, thus affecting food and feed quality as well as safety. Aflatoxin B1 is classified as a group 1 human carcinogen by the International Agency for Research on Cancer (IARC 2002).
Humans and animals are exposed to AFB1 through contact, ingestion, and inhalation. This exposure can lead to chronic and acute toxicity. Chronic exposure to AFB1 results in low to moderate AFB1 intoxication and this is linked to hepatocellular carcinogenesis. Acute AFB1 exposure by ingesting high doses of AFB1 causes hepatotoxicity (Benkerroum 2020). Aflatoxin B1 is metabolised in the liver by the cytochrome enzymes. The metabolic conversion of AFB1 generates a highly reactive AFB1 species known as AFB1-exo-epoxide and other reactive oxygen species such as hydroxyl radicals, superoxide anions, and hydrogen peroxide (Awuchi et al. 2021; Makhuvele et al. 2022). These reactive oxygen species can lead to DNA lesions, lipid peroxidation, and cell damage. Aflatoxin B1 toxicity differs among different species, with some organisms being more susceptible than others. The main mechanism of toxicity of AFB1 in both humans and animals is through the induction of oxidative stress (Lin et al. 2022).
Oxidative stress resulting from AFB1 can be equally prevented by the use of botanical extracts and synthetic antioxidants, but some synthetic antioxidants are toxic (Rasouli, Nayeri & Khodarahmi 2022). Botanicals have been used since the existence of humanity to treat various ailments and are part of a trillion dollar growing industry. The World Health Organization (WHO) has estimated that 80% of the world’s population still relies on herbal medicine to treat diseases with over 40% of pharmaceutical formulations derived from natural products (WHO 2018). Research has shown that botanical extracts possess protective agents that can act against toxicity of AFB1. Plants are known to possess compounds that can interact with reactive oxygen species (ROS) and protect the cell. They are rich in antioxidant, anticarcinogenic, and antimutagenic constituents, anti-inflammatory, hepatoprotective, and antigenotoxic constituents (Bansal & Chinmayee 2022; Makhuvele et al. 2020; Makhuvele et al. 2022). Curcumin is well-known for its chemoprotective and hepatoprotective properties against AFB1-induced hepatocarcinogenesis and hepatotoxicity in rodents, broilers, and ducklings (Dai et al. 2022; Mohajeri et al. 2018; Pauletto et al. 2020).
The Annonaceae family is among the most promising families against carcinogens (Emiliana et al. 2019; Nugraha et al. 2019; Yakubu et al. 2020). Annona senegalensis Persoon has been used in traditional medicine to treat microbial and parasitic infections and tumours in human and animals (Mulholland et al. 2000; Okhale et al. 2016). Previously, we reported the antigenotoxic potential of A. senegalensis against AFB1-induced genotoxicity in in vitro assays (Makhuvele et al. 2018). Furthermore, the antioxidant and hepatoprotective effect of stem bark extracts of A. senegalensis against carbon tetrachloride-induced damage was also reported (Omeke et al. 2019). Annona senegalensis has been reported to possess phytoconstituents including acetogenins, tannins, saponins, alkaloids, steroids, glycosides, anthocyanins, essential oils, and minerals, which have been reported to contribute to its anticancer activities (Al Kazman, Harnett & Hanrahan 2022; Okechukwu et al. 2023; Omeke et al. 2019). This study is aimed at investigating the hepatoprotective effects of hydromethanolic leaf extract of A. senegalensis against AFB1 toxicity on Sprague-Dawley rats using biochemical and histopathological parameters.
Research methods and designChemicals
AFB1 (≥ 98%) and curcumin (≥ 75%) were purchased from Sigma Aldrich. Propylene glycol (Univar grade) was bought from Merck, and methanol (HPLC grade) was obtained from VWR.
Plant collection and identification
Annona senegalensis (Annonaceae) leaves were collected from Lowveld National Botanical Gardens in Mpumalanga province of South Africa in March 2015. Mr. Willem Froneman from the South African National Biodiversity Institute confirmed the identity of the plant material. A voucher specimen (PRU 122755) was deposited at the H.G.W.J. Schweickerdt Herbarium of the University of Pretoria.
Plant processing
The leaf material of A. senegalensis was rinsed with distilled water to remove soil debris and dried in an oven set at 45°C for about 3 days. Thereafter, it was pulverised to a powder. Four hundred grams of the powdered plant material was exhaustedly extracted with 80% methanol by maceration at room temperature. Then, the plant extract was filtered through Whatman No.1 filter paper and concentrated to dryness using a rotary evaporator set at 40 oC to give a residue of 120 g (yield 30%).
Animal studies
The studies were carried out as described previously by Makhuvele et al. (2022).
Animals
Forty-eight healthy 7 week old Sprague-Dawley male rats (150 g – 200 g) were purchased from South African Vaccine Producers (SAVP) in Johannesburg, South Africa. The rats were caged in pairs with enrichment items such as wooden sticks for gnawing, tissue paper, and egg containers under a controlled temperature of ±22 oC, and humidity at ±50% in a light and dark cycle of 12 h. They were fed with a conventional rodent diet and water, available ad libitum for the duration of the study. The rats were allowed to acclimatise and were carefully monitored under laboratory conditions for 5 days prior to treatment. They were maintained as per the University of Pretoria Animal Ethics Committee with the protocol (V073-15) guidelines.
Hepatoprotective study
The rats were randomly grouped into six groups (n = 8). Group 1: did not receive any treatment (untreated control). Group 2: received 25% propylene glycol (negative control). Group 3: animals treated with 10 mg/kg body weight (b.w.) curcumin (positive control). The concentration of curcumin was selected based on the findings from previous studies where the dosage produced a marked antioxidant and potent hepatoprotective effect against aflatoxin B1 in other models of induced liver injury (Soni, Rajan & Kuttan 1992). The dose of Annona senegalensis leaf extract (ASLE) was selected based on previous studies conducted by Rotimi et al. (2017); Sathya, Kokilavani & Ananta Teepa (2012), while the dose of AFB1 was chosen based on studies by Rotimi et al. (2017); Zarev et al. (2020). Group 4–6 received 100, 200, and 300 mg/kg b.w. ASLE, respectively. All treatments were administered by oral gavage once a day for 7 consecutive days. On day 8 of the study, all rats (except the untreated control group) were treated with AFB1 (1 mg/kg b.w.) by oral gavage. After 72 h, the rats were euthanised with isoflurane, the livers were removed, and then fixed in 10% buffered formalin for histological analysis.
Determination of serum parameters
The protective effect of the ASLE was assessed by measuring the levels of the following serum enzymes: alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), lactate dehydrogenase (LDH), and creatinine. Blood samples were collected from the lateral tail vein of each rat on day 0 and by cardiac puncture on day 10 following anaesthesia with isoflurane and prior to sacrifice. The blood samples were sent to Clinpath diagnostic laboratory for evaluation of serum enzymes. The analysis was performed following Clinpath standard operating procedures using COBAS INTEGRA 400 kits plus automatic Chemistry Analyzer (Roche Diagnostics; Mannheim, Germany).
Histopathological studies
After euthanasia of the animals, the liver tissue samples were analysed for histopathological changes following standard methods for histopathological examination.
Statistical analysis
Analysis of variance (ANOVA) between the groups was performed using SAS version 9.3 (TS1M2). The standardised residuals were tested for deviations from normality using Shapiro–Wilk’s test. Data are presented as mean ± standard deviation. The data were considered significant at p ≤ 0.05.
Ethical considerations
Ethical clearance to conduct this study was obtained from the University of Pretoria Animal Ethics Committee (project no. V073-15).
ResultsEffect of treatment on animal well-being
All rats survived throughout the experimental period. No clinical signs of illness or abnormalities were reported in all rats treated with ASLE, or in the negative and positive control groups. The chosen dosages had no major effects on the physiology of the rats.
Effect of ASLE on aflatoxin B<sub>1</sub>-induced toxicity on selected serum enzymes
The effects of AFB1 intoxication as well as the hepatoprotective effect of ASLE and curcumin on serum biochemical parameters are presented in Figure 1a–e. A significant increase in the levels of ALT and AST was observed in the rats treated with AFB1 only (p < 0.001) when compared with ASLE+AFB1 (100 mg/kg, 200 mg/kg and 300 mg/kg b.w.) and curcumin + AFB1 groups, which exhibited a significant decrease in the levels of AST and ALT (p < 0.001). There was a tendency to a dose-dependent response to the plant extract ASLE, although no statistical difference was observed between the tested doses. Curcumin and ASLE (100 mg/kg b.w. – 300 mg/kg b.w.) reduced AFB1-induced increase of serum ALT and AST by 84% – 90% and 79% – 86%, respectively (Figure 2).
Effect of aflatoxin B1 on (a) alanine aminotransferase; (b) aspartate aminotransferase; (c) alkaline phosphatase; (d) lactate dehydrogenase and (e) creatinine levels of the rats treated with plant extracts and control substances. Data were expressed as mean ± s.d. (n = 8). Significant difference at p ≤ 0.05 is indicated by (*).
Percentage reduction of serum enzymes (alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, lactate dehydrogenase and creatinine) by curcumin and ASLE (100 mg/kg – 300 mg/kg) in relation to the AFB1 group.
Intoxication with AFB1 alone had no significant effect on the levels of ALP, LDH, and creatinine in the blood. No significant changes were observed in the levels of ALP (0.876), LDH (p = 0.800), and creatinine (p = 0.079) for the untreated group, AFB1 intoxicated group, curcumin + AFB1 and ASLE + AFB1 (100 mg/kg, 200 mg/kg and 300 mg/kg b.w.) treated groups. The relative AFB1 reduction of ALP was low, ranging between 4% and 16%, whereas the relative AFB1 reduction of creatinine and LDH was very low and similar to the control (Figure 2). This implies that AFB1 did not have any effect on the levels of ALP, LDH, and creatinine in all treatment groups.
Histopathological analysis
The histopathological analysis showed mild to moderate changes in the hepatic architecture of rats intoxicated with AFB1. The predominant hepatic lesions include hepatocellular injury with bile duct proliferation and hyperplasia, hydropic degeneration, necrosis, fibrosis, and portal lymphoplasmacytic infiltrates (Figure 3).
Photomicrograph of the liver cross section of a Sprague-Dawley rat (H&E, × 40). (a) Untreated control group; (b) AFB1-induced toxicity; slight to mild hepatocellular injury, bile duct proliferation (black arrow), lymphoplasmacytic infiltrate (red arrow), fibrosis (white arrow), normal bile duct (orange arrow). (c) AFB1+ curcumin; (d) AFB1+ ASLE 100 mg/kg; (e) AFB1+ ASLE 200 mg/kg; (f) AFB1+ ASLE 300 mg/kg showing the hepatoprotective effect of the ASLE and curcumin.
Discussion
This study investigated the protective effects of the hydromethanolic extract of A. senegalensis leaves against AFB1 hepatotoxicity. The outcomes of this study indicated that AFB1 significantly elevated the levels of AST and ALT in rats treated with AFB1 only. This increase in the levels of AST and ALT in the AFB1 treated group is an indication of hepatic oxidative damage as these enzymes are released into the blood only when there is tissue or cellular damage (Yakubu et al. 2020). The higher levels and higher standard deviations observed in the negative control group were because of inter-individual differences in the metabolism, bioavailability, and absorption of AFB1 by the rats. All tested doses of ASLE and curcumin were capable of ameliorating the hepatotoxic effect of AFB1, by normalising the serum levels of AST and ALT in the blood. These serum enzymes are found in low amount during a normal physiological state, but they increase in response to tissue or cell damage (Omeke et al. 2019). However, the highest concentration of ASLE was effective in preventing AFB1-induced damages comparably with the low concentration. Aflatoxin B1 intoxication did not have any effect on the levels of ALP, LDH, and creatinine in all treated groups. These results revealed that AFB1 did not have any effect on muscle metabolism in rats, as the levels of creatinine waste remained the same before and after AFB1 treatment.
Histopathological examination of rat organs was performed to support the results from the biochemical analysis. Aflatoxin B1 treatment resulted in mild to severe hepatocellular injury characterised by bile duct proliferation, necrosis, fibrosis, hydropic changes, and lymphoplasmacytic infiltrate. These findings are in accordance with the results from previous studies (Makhuvele et al. 2022; Yaman, Yener & Celik 2016). Aflatoxin B1 causes oxidative stress, necrosis, cirrhosis, hepatocellular injury, and liver cancer, as it is the main organ for AFB1 metabolism as also reported by Guo et al. (2023). Minimal histopathological architectural damages of hepatic tissues and cells were observed in AFB1-intoxicated rats treated with different doses of ASLE and curcumin. However, these injuries were noticeably reduced to slight signs of sub-lethal non-specific hepatocellular injuries in rats treated with ASLE and curcumin, thus indicating the ameliorative effects of the plant extracts against AFB1-induced hepatotoxicity. The protective effects of curcumin are attributed to its antioxidant capacity, which includes scavenging of ROS. Its mechanism of action involves inhibiting of activation of AFB1 by phase I enzymes and activation of phase II enzymes through activation of the Nrf2 signalling pathway and its downstream genes (Das & Vinayak 2015; Li et al. 2019; Muhammad et al. 2018). These findings are in line with the study by Omeke et al. (2019), which demonstrated potent hepatoprotective activity of A. senegalensis against carbon tetrachloride-induced liver damage in rats. Furthermore, Yakubu and coworkers (2020) showed the protective ability of the n-hexane extract of A. senegelensis against diethylnitrosamine-induced hepatocellular carcinoma. Previous studies in our laboratory reported the in vitro antigenotoxic effect of A. senegalensis against AFB1 (Makhuvele et al. 2018). The hepatoprotective effects of ASLE against AFB1-induced hepatoxicity may be because of the presence of phytoconstituents such as phenolic compounds including tannins, anthocyanins, found in A. senegalensis, which have been reported to contribute to its anticancer activities (Babalola et al. 2021; Yakubu et al. 2020).
Conclusion
The results obtained from this study demonstrated that ASLE has protective effects against AFB1-induced hepatotoxicity by reducing the levels of the serum enzymes AST and ALT and stimulating the hepatic regeneration. This protection is attributed to the induction of antioxidant activities by the phenolic contents of ASLE. Annona senegalensis is well-known in herbal medicine because of its biological activities against various ailments. Furthermore, determination of the bioactive phytoconstituents responsible for these protective activities and their mechanism of action is crucial for advancement of new hepatoprotective drugs and supplements.
Acknowledgements
The authors would like to thank the Lowveld National Botanical Garden for permission to collect plant material for the study. They also thank Mrs E. van Wyk for assisting with plant identification.
Competing interests
The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.
Authors’ contributions
E.E., L.P., L.V., and N.H. designed the study. R.M., K.F., and E.E. performed the experiments and analysed data. R.M. drafted the article. E.E., N.H., L.P., and L.V. revised the article.
Data availability
The data that support the findings of this study are available on request from the corresponding author, E.E.
Disclaimer
The views and opinions expressed in this article are those of the authors and are the product of professional research. It does not necessarily reflect the official policy or position of any affiliated institution, funder, agency, or that of the publisher. The authors are responsible for this article’s results, findings, and content.
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How to cite this article: Makhuvele, R., Foubert, K., Hermans, N., Pieters, L., Verschaeve, L., & Elgorashi, E., 2024, ‘Hepatoprotective effects of leaf extract of Annona senegalensis against aflatoxin B1 toxicity in rats’, Onderstepoort Journal of Veterinary Research 91(1), a2133. https://doi.org/10.4102/ojvr.v91i1.2133