The animal material consisted of 120 - 180 g Wistar rats acquired from the laboratory. Pharmacology and Improved Traditional Medicines (LPMTA) from the Faculty of Science and Technology (FAST), University of Abomey Calavi (UAC) and with the Experimental and Clinical Biology Unit (UBEC), Biotechnology Research Laboratory Medical and Pharmaceutical (LaRBiMeP), National School of Biosciences and Biotechnology of Dassa-Zoumé (ENSBBA), National University of Science, Technology and Engineering of Abomey (UNSTIM) in Benin. They were fed pelleted feed and water.

The collected sample was dried for three (3) weeks. It was then reduced to powder and stored in a suitable container for further handling. Extraction was dictated by bibliographical information on the chemistry of plant constituents. Ethanol was used as the solvent. Extraction took place in 3 stages: maceration, filtration and evaporation. 50 g of F. umbellata leaf powder is placed in 500 ml of ethanol. After maceration (for 72 hours), the product was filtered with filter paper, then with absorbent cotton placed in a funnel connected to a suction pump which accelerated filtration. After a few minutes, an exclusively liquid solution was obtained (the operation was repeated three times in succession). The filtrate obtained was placed in an oven at 45˚C to evaporate the ethanol. The dried extract was then scraped, weighed and the yield calculated.

Phytochemical screening was carried out according to the method used by Koutchiko [9] .

· Determination of total polyphenols

200 μl of extract was mixed with 1 ml of ten-fold diluted Folin-Ciocalteu reagent and 2 ml H₂O, and incubated at room temperature for 4 minutes. After adding 0.8 ml of 7.5% sodium bicarbonate to the mixture, total polyphenols were determined after 2 hours incubation at room temperature. Blue color absorbance was measured at λmax = 765 nm with a Shimadzu UV-VIS spectrophotometer. Quantification was performed using a standard curve for gallic acid at different concentrations (standard curve equation: y = 0.02x + 0.014 with R2 = 0.99). Results were expressed in milligrams of gallic acid equivalents (GAE) per g of dry extract.

· Determination of total flavonoids

1 ml of sample (prepared in methanol) was added to 1 ml of AlCl₃ solution (2% dissolved in methanol). After 10 minutes, absorbance was measured against the prepared reagent blank at λmax = 430 nm. Flavonoid concentrations were deduced from the calibration curve established with quercetin (0 - 35 μg/ml). Standard curve equation: y = 0.06x − 0.0002 with R2 = 0.98. Results were expressed in milligrams of quercetin equivalents per 1g of dry matter: mg EQ/1g of dry extract (mg EQ/g dry Ext).

· Determination of condensed tannins

Condensed tannins were determined using the vanillin method described by Julkumen-Titto. Vanillin reacts with free flavan-3-ols and the terminal units of proanthocyanidins, producing a red color whose intensity is proportional to the level of flavanols present in the medium, with an absorption maximum at 500 nm wavelength. Aliquots of 0.1 to 1 ml of the catechin stock solution (0.5 mg/ml) and extracts were introduced into a series of test tubes, the final volume in each tube being made up to 1 ml by addition of absolute methanol. 1.5 ml of 4% vanillin solubilized in methanol and 750 μl of 37% HCl (12M) were added at 1-minute intervals to each tube in the series and then placed in a water bath at 30˚C for 20 minutes. Results were expressed as milligrams of Catechin Equivalents (mg CE) per 1g of dry matter.

This study was conducted in accordance with OECD guideline 423 for the testing of chemicals [10] . At the start of the test, 8-week-old rats weighing between 120g and 180g were randomly selected. They were marked for individual identification and kept in their cages. Four (4) batches of three (3) rats were formed. One received only distilled water orally, while the other three received a single dose of 1000, 3000 and 5000mg/Kg B.W. respectively (as no information was available on the regulatory dose limit) of ethanolic extract of F. umbellata dissolved in physiological water. Animals were observed individually half an hour after administration of the extract, one hour later, and then daily. Samples were taken on D0 before and 14 days after administration of the extract. All observations were systematically recorded. Fourteen days later, the animals were sacrificed. Kidneys, liver and spleen were removed for histological study.

· Body weight

Individual rat body weights were taken before extract administration, on D0 and then on D14. Weight variations were calculated and recorded.

· Biochemical tests

Biochemical parameters (bilirubin, AST, ALT, ALP, urea, creatinemia, uric acid) were determined using a Mindray-BS 240 automated system.

· Hematological tests

Hematological parameters were determined using a “SYSMEX XN-330” automated system. This machine counts white blood cells, red blood cells and platelets, and determines hemoglobin, hematocrit, Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Concentration and Average platelet Hemoglobin Content.

Kidneys, liver and spleen were removed, fixed in 10% buffered formalin and embedded in kerosene. Sections of the samples (5 μm) were mounted on glass slides, deparaffinized and hydrated. For histological analysis, sections are stained with hematoxylin and eosin (H&E), following a standard protocol [11] . Photographs are taken at 400 X magnification.

The study of the anti-inflammatory activity of the ethanolic extract of F. umbellata was conducted following the method described by Rahmani [12] and slightly improved. Rats were given the extract at doses of 100, 300 and 500 mg/Kg or aspirin at a concentration of 100 mg/Kg PC orally, one hour before injection of 0.05 mL of 1% formalin under the plantar fascia of the rat’s right hind paw. Paw volume measurements were taken one, two and three hours after formalin injection, using an electronic caliper. Anti-inflammatory activity was assessed in terms of percentage reduction in edema in treated rats versus controls, using the following formula:

Percentage ( % ) ofinhibition = ( % ) increase control − ( % ) increase treaty ( % ) increase control × 100

¾ % increase control: percentage (%) of average increase in circumference of edematous leg in control group.

¾ % increase treaty: percentage (%) of average increase in circumference of the edematized leg in the treatment group.

% increase = V t − V 0 V 0 × 100

V₀: volume of paw at t = 0 (before formalin injection).

V_t: paw volume at any time t.

Data collected before and after treatment with the extract were tabulated and entered into Excel 2013. Normality and homogeneity of variances were checked with R Studio software using the Shapiro.test and Levene.test respectively; comparison of pre- and post-treatment data was carried out using the parametric paired two-sample test with R Studio software. Histograms showing the comparison of the mean rate of each parameter were produced using Graphpad Prism 9.5.1 (733) software. Significance is declared when the probability value P-value is less than 0.05.

Extraction yield is calculated as the ratio between the mass of extract and the mass of leaf powder.

Yield = (Mass of extract/Mass of dry leaf powder) × 100

Yield = (30.55/150) × 100

The extraction yield was 20.37%. The extract has a black color.

Phytochemical screening enabled us to identify the various secondary metabolites contained in F. umbellata dried leaf powder. The qualitative results of this phytochemical screening test are summarized in Table 1.

Total polyphenol, flavonoid and tannin contents are shown in Table 2. Total polyphenols are higher (125.65 ± 2.1 mgEAG/g dry extract) than flavonoids and tannins.

The actions of the animals were carefully observed during the first 30 minutes after administration of the extract and throughout the 14 days of experimentation. It was noted that, apart from drowsiness, rats treated with 1000 and 3000 mg/Kg∙BW showed no clinical signs, whereas those treated with 5000 mg/Kg∙BW showed diarrhea, tremors and accelerated breathing. The results obtained are summarized in Table 3.

(+): Presence; (−): Absence.

a: milligram of gallic acid per 1 gram of dry extract (mg EAG/g of dry extract); b: milligram of quercetin equivalents per 1 gram of dry extract (mgEQ/g of dry extract); c: milligram of Catechin Equivalents per 1 gram of dry extract (mgEC/g of dry extract).

(+): Presence of sign; (−): Absence of sign.

After 14 days of observation, no deaths were observed, so the LD50 value for ethanolic extract of Ficus umbellata leaves is greater than 5000 mg/Kg body weight.

Figure 1 shows the effect of the extract on animal body weight over the course of the experiment as a function of time. Analysis of the variation in body weight of animals given different oral doses of the extract showed a reduction in weight from Day 7 onwards. There was a downward trend in weight from Day 0 to Day 7 (p > 0.05). On Day 14, the decrease was very pronounced (p < 0.0024).

Statistical analysis of the haemograms of the control and test batches showed that only blood platelets showed a significant difference from the control for doses of 3000 and 5000mg/Kg∙BW (p < 0.05). The results obtained are summarized in Table 4.

Statistical analysis of the blood counts of the control and test batches showed that only blood platelets showed a significant difference from the control for the 3000 and 5000 mg/Kg∙BW (p < 0.05).

Figure 2 shows the effect of F. umbellata ethanolic extract on conjugated bilirubin levels in rats. Conjugated bilirubin levels in the batches tested showed an upward trend at day 14. Analysis of variance results showed no significant difference whatever the dose administered (p > 0.05).

Figure 3 shows the effect of ethanolic extract of F. umbellata on total bilirubin

A = statistically insignificant difference (p > 0.05); b = statistically significant difference (p < 0.05); MCHC: Mean Corpuscular Hemoglobin Concentration; VGM: Mean Corpuscular Volume; AHC: Average platelet Hemoglobin Content.

levels in rats during experimentation. An increase in total bilirubin was observed in rat batches given 3000 and 5000 mg/Kg∙BW with p < 0.01.

Figure 4 shows the effect of ethanolic extract of F. umbellata on creatinine levels in rats during experimentation. Creatinine levels in the test batches showed no significant difference from the control (p > 0.05) on day 14.

Figure 5 shows the effect of ethanolic extract of F. umbellata on urea levels in rats. The urea levels of experimental batches given 5000 mg/Kg∙BW increased with p < 0.05 after 14 days.

Figure 6 shows the effect of ethanolic extract of F. umbellata on uric acid levels in rats during experimentation. It shows that uric acid levels increased in batches of experimental animals given doses of 3000 mg/Kg∙BW (p < 0.05) and 5000 mg/Kg∙BW (p < 0.01) after 14 days. Table 6 summarizes the effect of ethanolic extract of F. umbellata leaves on the various biochemical parameters assessed.

Figure 7 and Figure 8 show the effect of ethanolic extract of F. umbellata on AST and ALT levels in rats during the course of the experiment. After 14 days, the transaminase values (ALT and AST) of the test batches only really increased with the 5000 mg/Kg∙BW dose (p < 0.05), precisely at the ALT level.

Figure 9 shows the effect of F. umbellata ethanolic extract on alkaline phosphatase

levels in rats during experimentation. Alkaline phosphatase levels in the test batches increased on day 14 (p < 0.05) with doses of 3000 and 5000 mg/Kg∙BW.

Ethanolic extract of Ficus umbellata had no significant effect on the weight of harvested organs. The results obtained are summarized in Table 5.

· Liver histology

Liver histology of rats treated with ethanolic extract of Ficus umbellata leaves was as follows:

The livers of rats treated with various doses of Ficus umbellata extract showed no visible atypia. Normal-looking hepatocytes (arrows) were arranged in radial cords around the centrilobular vein (CV). The venous sinusoids (S) are clearly

NS: Not Significant.

Data are presented as mean ± standard deviation; *: significant difference p < 0.05; **: significant difference at p < 0.01.

visible, as observed in control rats (Figure 10).

· Renal histology

Renal histology of rats subjected to ethanolic extract of Ficus umbellata leaves is as follows:

The renal parenchyma of rats treated with Ficus umbellata extract retained its typical appearance as observed in control rats. Glomeruli (G), proximal tubules (PT), distal tubules (DT) and collecting ducts (CC) showed no visible atypia (Figure 11).

· Splenic histology

Splenic histology of rats under the influence of ethanolic extract of Ficus umbellata leaves was as follows:

The splenic parenchyma was not activated in the acute oral toxicity test. As in control rats, the periarteriolar (MA) lymphocyte mantles around the central arteries (CA) and the germinal centers (GC) of the white pulp showed the typical appearance. The same applies to the sinusoids (S) and Billroth cords of the red pulp (Figure 12).

· Percentage increase in hind leg oedema in rats treated with ethanolic extract of F. umbellata as a function of time

Administration of ethanolic extract of F. umbellata at doses of 100 and 300 mg/Kg body weight (BW) significantly (p < 0.05) prevented 1% formalin-induced edema of the rat paw. The percentage increase in inflammatory paw oedema was 34.54 ± 2.73; 41.49 ± 5.56; 59.61 ± 1.81 for rats treated with 100 mg/Kg and 23.21 ± 2.13; 40.14 ± 2.27; 53.83 ± 4.04 for rats treated with 300 mg/Kg. compared with the control group treated with physiological water, whose edema increased by 41.31 ± 1.79; 75.24 ± 2.86 and 114.32 ± 6.86, respectively at 1, 3 and 5 hours after injection of 1% formalin. At 500 mg/Kg body weight, F. umbellata ethanolic extract showed better prevention of 1% formalin-induced paw edema than at 100 and 300 mg/Kg body weight. The percentages of increase in inflammatory paw edema were lower, at: 15.98 ± 1.62; 26.26 ± 1.42 and 35.19 ± 2.84, respectively at 1, 3 and 5 hours after injection of 1% formalin. Table 7 shows the percentage increase in hind leg oedema in rats as a function of time.

Data are presented as mean ± standard deviation *: significant difference at p < 0.05.

Data are presented as mean ± standard deviation; *: significant difference at p < 0.05; **: significant difference at p < 0.01.

· Percentage inhibition of hind paw oedema as a function of time in rats treated with Ethanolic extract of F. umbellata

Evaluation of the percentage inhibition showed that the extract had greater anti-inflammatory activity 3 hours later. However, a better inhibition of inflammatory paw edema at 500 mg/Kg∙BW was observed at 5 hours with a percentage of 69.23 ± 1.02 compared to the reference group treated with aspirin 100 mg/Kg which showed an inhibition of 63.50 ± 0.98. Table 8 shows the percentage inhibition of hind-paw edema in rats as a function of time.