Sub-acute Toxicity of Aqueous Extracts of Tephrosia vogelii, Vernonia amygdalina and Senna occidentalis in Rats

Sub-acute Toxicity of Aqueous Extracts of Tephrosia vogelii, Vernonia amygdalina and Senna occidentalis in Rats Immaculate Nabukenya1*, Chris Rubaire-Akiiki1, Denis Mugizi1, John Kateregga1, Deogracious Olila1 and Johan Höglund2 1College of Veterinary Medicine, Animal Resources and Biosecurity, Makerere University, P.O. Box 7062, Kampala, Uganda 2Department of Biomedical Sciences and Veterinary Public Health, Section for Parasitology, Swedish University of Agricultural Sciences, P.O. Box 7063, Uppsala, Sweden


Background
Uganda has 80% of its population depending on agriculture and about 50% are engaged in livestock farming [1]. In small-scale livestock production, majority of the farmers use a combination of conventional and ethnopharmacological formulations to treat diseases and parasite infections [2,3]. Use of plants in animal disease treatment is practiced traditionally [2,[4][5][6], albeit with non-standardised doses as a major shortfall [4,7,8]. This is further compounded by the basic belief that plant extracts are non-toxic [2,7,9]. In an earlier study mapping ethnopharmacological practices in Mpigi and Gulu districts in Uganda, farmers prioritized Vernonia amygdalina (VA), Tephrosia vogelii (TV) and Senna occidentalis (SO) for detailed evaluation [3].

Plant collection and extract preparation
Fresh leaves of all plants were collected in January 2013 from wild shrubs at Mbarara Zonal Agricultural Research Development Institute farm, located 274 km south-west of Kampala, the capital of Uganda. The voucher specimens were confirmed by a botanist and deposited in Makerere University Herbarium (numbers SO -NI 02, VA -NI 03 and TV -NI 04). The leaves were dried under shade in the laboratory for two weeks. They were ground to fine powder with an automated electric grinder (Grindomix, Retsch, GM 200). For aqueous extraction, 500 g of powder from each plant was infused in 2 l of hot distilled water for 24 hours with regular stirring (metallic magnet). After filtration with a 4 mm Whatmann filter paper, the filtrate was freeze dried at -82°C. The dried extracts were weighed and stored at 4°C until needed. acute study. In the protocol, OECD test guidelines were followed [29]. National Academies guide for the care and use of laboratory animals [30] were adapted for the animal protocol in this study and was approved by the institutional review board (study number IRBCOVAB/2013/009). Briefly, 100 Wistar white albino rats (50 females and 50 males), of about 6 to 8 weeks old weighing 70-100 g were procured from Uganda Virus Research Institute and kept for two weeks to acclimatize to the new laboratory conditions. Each extract was reconstituted in Goodwin's physiological solution to a stock concentration of 200 mg/ml. The rats were weighed and randomly assigned to 10 treatment groups i.e. of each extract, 200 mg/kg, 400 mg/kg and 600 mg/kg body weight plus the negative control (given Goodwin's physiological solution w/v). In each group, the number of females and males was equal. Each group was kept in 80x50 cm wooden cages, fed on commercial rodent feed (Unga Limited, Kenya) and given water ad libitum. The rats were treated once daily, while body weights were taken once a week and on the 29 th day, before termination of the experiment.

Sample collection
On the 29 th day, the rats were weighed, anaesthetised with 70% chloroform (trichloromethane, E08A/0808/2104/13, Fine-Chem, India) for ten minutes before blood and tissue collection. Whole blood collected by cardiac puncture was transferred into labelled plain and EDTA vaccutainer tubes (BD Plymouth, UK). EDTA blood was kept at 4°C while non-EDTA blood was centrifuged at 1500 g for three minutes to separate serum, which was kept at -20°C. The rats were then dissected to collect the liver, kidneys, small intestine sections, heart and lungs; which were weighed and kept in 10% buffered formalin for histopathology.

Haematological and biochemical tests
The EDTA whole blood for haematology was processed within 24 hours as described previously [31]. The automated haematological analyser (Coulter STKS, Beckman) was used to obtain the following; white blood cell counts (WBC), differential counts of neutrophils, lymphocytes, monocytes, oesinophils and basophils; red blood cells (RBC), haemoglobin (Hb), haematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular haemoglobin concentration (MCHC), mean corpuscular haemoglobin (MCH), red blood cell width to corpuscular volume (RDW-CV), mean platelet volume (MPV) and platelets (PLT). Serum kept at -20°C was thawed to 25°C and processed within two days after collection in the clinical chemistry laboratory at Mulago Hospital. Biochemical analysis using an automated analyser (Medonic, CA620, Boule, Sweden) was conducted for blood urea nitrogen (BUN), creatinine, Aspartate aminotransferase (AST), alanine aminotransferase (ALT), uric acid (UA), total cholesterol, triglycerides, alkaline phosphatase (ALP), total protein (TP), albumin, total and direct bilirubin. The control group mean values were used as the baseline for comparison with treatment groups.

Histopathology
Whole rat organs kept in 10% buffered formalin for two weeks were processed in the Central Diagnostic Laboratory of the College of Veterinary Medicine at Makerere University. Sections of the liver, kidney, lung, small intestines and heart were prepared as described previously [31,32]. Sections were stained with Haemotoxylin and Eosin (H&E), and then microscopically examined for pathological changes at x10, 20 and 40 magnifications.

Data analysis
Laboratory data was entered in Microsoft Excel ® and analysed in Minitab 16.0 (Minitab Inc., USA). Means, standard deviation, standard error of the mean, median and 95% confidence intervals of ontinuous variables were calculated and plotted by a pre-designed Excel sheet [33]. One-way analysis of variance (ANOVA) and Tukey's high square difference test were used to compare mean differences for different parameters in the treatment and control groups. Proportions and percentages were computed and compared across groups using the Mann-Whitney, Newman-Keuls and Chi-square tests. The level of significance was set at P<0.05.

Physical signs and gross necropsy findings
In all treatment groups, we observed no changes in feed and water intake. There were three deaths (one each at 600 mg/kg of TV, SO and VA) after 15, 24 and 26 days after treatment respectively. The immediate cause was wounds due to cannibalism, but after housing the rats individually, no more deaths were registered. No pathological gross necropsy findings were detected in treated and control rats during organ collection and processing.

Effect on body, heart, liver and kidney weights
There was a gradual increase in body weight in rats across all treatment groups but mean weight of SO 600 mg/kg was lower than other groups at day 0 and 14. However, the difference was non-existent by day 21 and at the end of experiment (day 29). There was less variation of mean post-mortem weight of the kidney and liver in the treatment groups. Although the liver weights ranged from 4.6-9.7 g, there was no statistical difference in mean weights due to treatment.

Effect on biochemical and haematological parameters
The extracts caused varied effects on haematology and biochemistry (Table 1). For example, there was depression of haematocrit in a doseresponse pattern, whereas the WBC counts were much higher in the control (19.6 ± 10.5x10 3 /µl) compared to other groups (<15 x10 3 /µl). A reverse relationship was observed with RDCHV; showing elevated levels with increasing doses for all plant extracts but there was minimal change in MCHC. At increasing doses, TV had a significant reducing effect on the mean platelet counts compared to other treatment groups and the controls (  Figure 1A and 1B). Furthermore, albumin protein was elevated in SO and VA in dose-response manner compared to TV, which led to a small change ( Table 2). The elevation was significant at 600 mg/kg of SO (44.9 g/L) and VA (47.8 g/L) compared to TV (38.2 g/L) and control group (34.8 g/L).

Histopathology and microscopic effects of the treatments
As shown in Table 3 and Figure 2A-2F, there were varied effects of treatments on the histopathology of the liver, kidney, lung, heart and small intestines. TV caused more toxic changes in the organs compared to SO and VA. For example, at TV 600 mg/kg, villi sloughing in intestines, myocardial and renal congestion as well as hyaline degeneration of the liver were recorded. Slight pneumonitis in the lungs with mononuclear cell infiltration was also noted in TV 600 mg/ kg ( Figure 2). Most of the changes followed a dose-response pattern.

Discussion
The geographical location, season, soil type, climate differences, agronomic practices, plant part and age affect the concentration of phytochemicals, usually leading to differences in bioactivity and toxicity [7,16,18]. Using proteomics, metabolomics and transcriptomics in recent advances to determine nephrotoxic, genotoxic and teratogenic effects of natural plant products has been recommended [34]. These in silico, in vitro and in vivo methods which may explain the mechanisms of action, are however still unstandardised [34]. Following the established protocol [29,33], the recommended number of animals used supported statistical analysis.
The difference in concentration of phytochemicals extracted by various solvent systems may account for differences in observed toxicity of a plant extract at the same doses. For example, saponins are incriminated to cause haemolysis [35]. Although VA has significant levels of saponins [36,37], there was a dose-dependent increase in RBC counts. On the contrary, a reduction in RCB counts with increasing doses of SO and TV and PCV was noted. This is a possible mechanism of toxicity for the latter two extracts. Although no specific study on effect of extract on platelet count was done, we observed a marked reduction in platelets in higher dose groups of TV (363 and 398 compared to 734x10 3 /µl in control). When platelets are significantly reduced, there may be multiple organ failure, eventually leading to toxicity signs or death.
Specifically, rotenone present in TV [11,38], causes similar signs of poisoning in humans and is one of the possible chemicals responsible for the observed acute toxicity [21]. In insects and fish, rotenone interferes with mitochondrial electron transport system, whereas mammals are more tolerant [38]. Rotenone however, is less soluble in water and easily disintegrates in the environment [12] which explains the presently observed reduced toxicity by aqueous extracts. Anthracenosides and anthocyanosides have been incriminated as toxic phytochemicals previously. However, qualitative phytochemistry (results not presented here) showed both anthracenosides and anthocyanosides in the aqueous extract of TV and VA.  C3 CT4 T5 T6 T7 V10 V8 V9  C1 C2 C3 CT4 T5 T6 T7 V10 V8 V9  ALT u re a C 1 U ri c A c id B il ir u b in   The seeds of SO are reportedly toxic to many vertebrates and the unnamed toxic albumin is incriminated [18]. This study however, considered only the leaf extracts and thus some of these toxic rinciples may have been in limited amounts (no specific tests done presently). Some of the phytochemicals in SO are reported to be hepatoprotective [18,39]. In the current study, the 600 mg/kg dose of aqueous extracts of SO exerted significant decrease in AST, ALT enzymes but increased urea and uric acid compared to the controls and other treatment groups. These results support previous findings that the SO leaf extract is hepatoprotective [39]. On the contrary, in a previous study, there was no change in liver enzymes and haematological parameters in female and male rats for SO at doses as high as 2500 mg/kg/day [28]. Their study therefore, did not report any toxicity of SO in the male or female rats. SO and VA caused similar biochemical changes in the rats. For example, they both caused depression of ALT and AST in a doseresponse manner; quite the opposite to the effect of TV (elevation with higher doses). In addition, they both caused an elevation in albumin protein. Depression of this protein clearly indicates chronic liver damage compared to elevation of ALT and AST (sometimes caused by muscle damage), thus a better indicator of liver function. This further confirms the hepatoprotective effect of SO and VA as previously discussed [13,23,39].
Although there were no visible gross changes observed in the sampled organs, histopathology results indicated more toxic effects by TV compared to SO and VA. Sloughing of the intestinal villi observed in SO and TV due to continued necrosis can lead to reduced nutrient absorption, which will eventually impair liver and kidney function. Antioxidant activity of SO by reducing DNA degeneration (iron IIdriven Fenton reaction) has been demonstrated with seed extracts. Inhibition of DNA damage by strong ion chelation activity is also hepatoprotective [18,40]. In chicken, studies demonstrated lower phosphorylation ratios and respiratory control ratios and oxygen use in liver mitochondria [18]. Pneumonitis, mononuclear cell infiltration and lymphoid necrosis as observed in some cases in this study lead to compromised gaseous exchange and eventual death. Underlying toxicity mechanisms at cellular level should be undertaken with standardised proteomics, metabolomics and transcriptomics.

Conclusion
SO and VA were hepatoprotective while TV was slightly hepatotoxic in a dose response manner. The very low toxicity of the aqueous leaf extracts of TV, VA and SO at high doses provide for its safety within the irregular and unstandardized doses used for human and animal treatment. Focal areas of hepatic degeneration (pykinosis) were identified in TV 600 dose Table 3: Histopathology findings in the liver, kidney, lung, heart and small intestines of 40 rats after 28 days daily oral treatment at 200, 400 and 600 mg/kg of the three plant extracts.