Antioxidant property, haematinic and biosafety effect of Ipomoea batatas lam. leaf extract in animal model
Beni-Suef University Journal of Basic and Applied Sciences volume 10, Article number: 75 (2021)
Plant medicine was dated back for decades and has immensely contributed to the health care system in several countries. This present study evaluated in vitro antioxidant, anti-anaemic and biosafety properties of n-hexane leaf extract of Ipomoea batatas L. in an animal model. The antioxidant property of the extract was expressed by 1, 1-diphenyl-1-picrylhydrazyl (DPPH) with an appropriate method. The extract was orally administered at graded doses (125, 250 and 500 mg/kg body weight) to determine its effect on 40 mg/kg phenylhydrazine hydrochloride-induced anaemia in rats at days 1, 7 and 14 using a standard protocol. Acute and subacute toxicological evaluations were based on initial behaviour, mortality and histological examination of the organs.
The antioxidant study of the extract showed 60.14% in the presence of DPPH and ascorbic acid. The haematological parameters (RBC, HGB, HCT, MCV, MCH and MCHC) significantly increased at p value < 0.05 in the treated groups compared with control groups. Specifically, there is a significant increase in the treatment groups, namely red blood cells (5.93, 6.78, 6.75), haematocrit (40.75, 44.05, 44.63) and haemoglobin (13.35, 14.70, 14.73), when compared with untreated control. Also, the results of the myeloid/erythroid ratio of the treated groups (20: 40, 21.7: 43.4 ratio) and (23. 3: 46.6 ratio) are compared with (15.0: 25.0 ratio) of 40 mg/kg phenylhydrazine and 25: 50 normal control of the bone marrow at day 14. No acute behavioural change or mortality was observed. Histological analysis exhibited normal physiological state of the visceral organs.
These findings support the folklore use of Ipomoea batatas L. leaf extract to reduce oxidative stress, treat anaemia and exhibit its safety at the highest doses of 500 mg/kg body weight.
Plants having medicinal properties are helpful in herbal practices and can be broadly used to heal several diseases possibly due to their phytoconstituents . Phytochemicals in a plant are natural chemical components present in varying amounts in plant parts (leaves, vegetables and roots), with defence mechanisms to manage several diseases. Sweet potatoes, botanically called Ipomoea batatas L., are one of the earliest plants used by traditional healers to treat different illnesses. I. batatas is from the family 'Convolvulaceae', a dicotyledon having two embryonic seed leaves . Ipomoea batatas L. has been indicated to possess a broad folklore relevance in anti-inflammatory, anti-fertility, anti-carcinogenesis, anti-mutagenicity and anti-diabetes properties, including promoting stable blood sugar levels; they are rich in polyphenols such as caffeoylquinic acid derivatives .
On the other hand, anaemia is known to be a global health crises affecting both developed and developing nations. The World Health Organization defines it as a state where several red blood cells or their oxygen-carrying capacity (haemoglobin) is not being sufficient to meet physiologic needs with respect to age and lifestyle habits such as smoking, sex and pregnancy status . Studies have reported annual cases as high as 19.7% of anaemia in children, with rural inhabitants taking the more significant proportion [5, 6]. Anaemia is classified into various types, and haemolytic anaemia is one of its kind [7, 8]. Currently, several studies have shown that I. batatas exhibit antioxidative or radical-scavenging phytochemicals with health-enhancing activity in humans [3,4,5]. Also, evidence has shown that sweet potatoes possess a pivot antioxidant property because of their high quantity of flavonoids, phenols, β-carotene, anthocyanins and caffeoylquinic acid derivatives . These constituents have been implicated in the correction of heart abnormalities . It is believed that mucilage present in them might be responsible for their antioxidant effects against hydroxyl and peroxyl radicals  as much as alternate remedies have great potential in treating illness. Plants with toxic compound can result in organ damage and death. This study therefore evaluates the biosafety, anti-anaemic and in vitro antioxidant property of Ipomoea batatas L. leave extract.
2.1 Collection of plant material
Sweet potatoes leaf (Ipomoea batatas L.) was collected from Bolorunduro village Akure, in Ondo State, Nigeria, identified and authenticated by Dr. O. Timothy of the Department of Plant Biology and Biotechnology, University of Benin, Edo State, Nigeria, with voucher number UBH-B473.
2.2 Preparation of plant material
The leaves were rinsed and air-dried for three days, after which oven-dried at 40 °C for few hours. The crunchy leaves were reduced to powder using an electrically powered engine. The powdered sample was stored in a moisture-free, airtight container until further use.
2.3 Determination of total antioxidant activity
The antioxidative activity of the plant extract was studied as the free radical-scavenging effect on the 2, 2-diphenyl-1-picrylhydrazyl radical and determined by UV spectrophotometry at 517 nm. Radical scavenging activity was measured by a slightly modified method previously described by Dini et al. , using 20–100 µg/ml of the crude extract and ascorbic acid prepared in methanol (analytical grade). After that, 1 ml of the plant extract was placed in a test tube, with 2 ml of 0.1 Mm DPPH in methanol. A control solution was prepared to contain the same amount of methanol and DPPH. The radical scavenging activity was calculated using the following formula.
where Ab is the absorption of the blank sample and Aa is the absorption of the plant extract.
2.4 Experimental animals
Fifty-four (54) male albino rats weighing between 180 and 250 g were obtained from the animal house of the Pharmacology Department, University of Benin, Benin City. They were housed in conducive cages and allowed free access to rat chow and water and acclimatize for two weeks. The animals were handled according to standard protocols for the use of laboratory animals approved by the ethical committee of the Faculty of Life Sciences with ethical number LS17101.
2.5 Experimental design
Six (6) groups labelled A–F were designed for this study, each group having nine (9) rats housed in separate cages. Groups A, B, D, E and F were induced with 40 mg/kg phenylhydrazine hydrochloride for five (5) days orally, while group C was given distilled water alone. The animals were post-treated with oral administration of distilled water, 5 mg/kg ferrous (iii) hydroxide poly-maltose or groups A and B and 125, 250 mg/kg and 500 mg/kg n-hexane plant extract for groups D, E, and F, respectively, for days 1, 7 and 14. The rats' body mass indexes were taken and recorded every week.
2.5.1 Haematology assays
Three (3) millilitres of blood was collected from each group at days 1, 7 and 14 into 5-ml EDTA tubes by cardiac puncture using syringes and needles. The haematological analysis was done almost immediately using an automatic haemato-analyzer (Sysmex, KX-21, Japan). The parameters measured included red blood cells (RBCs), haemoglobin (HGB), haematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH) and mean corpuscular haemoglobin concentration (MCHC).
2.5.2 Peripheral blood film
The slides were cleaned with 70—90% alcohol and allowed to air dry. The middle or ring finger was selected to make a hole. The area was washed with 70% ethyl alcohol and punctured. A drop of blood was touched to the clean slide. Blood was spread on the glass slide by another slide. It was repeated with several slides. Slides were dried and fixed with methanol. Photomicrographs were taken at × 40 using a digital camera.
2.5.3 Bone marrow preparation
Bone marrow from the femur bones was isolated and fixed in 10% (vol/vol) formaldehyde, cleaned up in xylene and decalcified to be embedded in a paraffin wax (melting point at 56%) according to the method of Ogwumike  and stained with eosin/haematoxylin. Photomicrographs were taken at × 40 using a digital camera.
2.6 Acute toxicity study
Determination of acute toxicity was performed using a modified method by Lorke  and class method in adherence to the Organization for Economic Cooperation and Development (OECD) Guideline for Testing Chemicals No. 423 OECD, . This was performed in two phases. In phase 1, forty-five (45) mice were randomly divided into nine (9) groups of five (5) each. Ipomoea batatas L. n-hexane leaves extract was administered in single dose of 10, 100 and 1000 mg/kg) orally. Observable toxicological signs were recorded. With the absence of toxicity, the second phase experimented. Based on the acquired results from phase 1, phase 2 is scheduled with three (3) mice per group administered a single dose (1600, 2,900 and 5,000 mg/kg) of I. batatas n-hexane leaves extract orally. The animals in both phases were kept under the same conditions and observed for general behaviour changes continuously for 30 min, every hour during the first 24 h and at least once daily for 14 days after administration of the extract. Observations were focused on parameters such as piloerection, sensitivity to sound and touch, locomotion, aggressiveness, the appearance of faeces, salivation, urinating, convulsing, coma and death. The number of survivors was noted after 24 h. Animals' weights were observed for days 0, 7 and 14. The LD50 was evaluated and classified according to the Globally Harmonized System (GHS) for the classification of chemicals [12, 13]. The LD50 was calculated based on the final results in the square root of the product of the lowest lethal dose and the highest non-lethal dose, i.e. the geometric mean of the consecutive doses, where 0 and 100% survival rates were recorded.
Every rat used in the acute toxicity study experimented daily for possible toxicity signs over two weeks.
The LD50 is calculated using the formula:
D0 = Highest dose that gave no mortality, D100 = Lowest dose that produced mortality.
2.7 Histological study
The organs (liver, kidney, heart and spleen) were fixed in 10% (vol/ vol) formaldehyde, cleaned up in xylene and embedded in a paraffin wax (melting point at 56 percent). Tissue sections were prepared according to Drury and Wallinton  and stained with eosin/haematoxylin. Photomicrographs were taken at × 400 using a digital camera.
2.8 Statistical analysis
Data were presented as mean ± SEM of the respective replicates. Means of different groups were compared using ANOVA using GraphPad prism version 6 computer software packages. P values ≤ 0.05 (95% confidence interval) were considered significant.
The results of the total antioxidant activity of n-hexane extract of Ipomoea batatas L. are indicated in Fig. 1. The n-hexane extract was observed to possess the highest free radical scavenging potential with percentage inhibition of 39.21 ± 1.70% at 100 µg/ml when compared with the standard (ascorbic acid) 89.02 ± 2.21 at 100 µg/ml.
3.2 Anti-anaemic study
Figure 2 shows a significant decrease in red blood cell count across groups A, B, D, E and F on day 1 of the experiment with a subsequent increase on day 7 and a significant increase on day 14 of the investigation after treatment with n-hexane leaves extract of I. batatas. Figure 3 also shows a significant decrease in packed cell volume across groups A, B, D, E and F on day 1 of the experiment with subsequent increase on days 7 and 14 after treatment with n-hexane leaves extract of I. batatas. Our results also showed a significant decrease in haemoglobin across groups A, B, D, E and F on day 1 of the experiment with subsequent increase on day 14 of the experiment after treatment with n-hexane leaves extract I. batatas in Fig. 4.
Similarly, Fig. 5 presents the effect of I. batatas n-hexane leaves extract on mean corpuscular volume (MCV) fl in phenylhydrazine-induced anaemia. The results showed a significant decrease in mean corpuscular volume across groups A, B, D, E and F on day 1 of the experiment with a subsequent increase on day 7 with a significant increase on day 14 of the investigation after treatment with n-hexane leaves extract of I. batatas. Likewise, Fig. 6 observes a substantial decrease in mean corpuscular haemoglobin concentration (MCHC) across groups A, B, D, E and F on day 1 of the experiment with a subsequent increase on days 7 and 14 of the investigation after treatment with n-hexane leaves extract of I. batatas.
Additionally, the effect of I. batatas n-hexane leaves extract on mean corpuscular haemoglobin (MCH) pg in phenylhydrazine-induced anaemia is presented in Fig. 7. The results revealed that a similar trend for other parameters was observed with a significant decrease in mean corpuscular haemoglobin concentration across groups A, B, D, E and F on day 1 of the experiment with a subsequent increase on day 14 of the investigation after treatment with n-hexane leaves extract of I. batatas.
The result of the study showed that the administration of the graded dose of n-hexane extracts induced normochromic and normocytic cells on the damaged red blood cells on day 14. This revealed a strong effect of the extract on red blood cells compared with the group that received 40 mg/kg phenylhydrazine hydrochloride and 5 mg/kg of ferrous (iii) hydroxide (Fig. 8).
3.3 Bone marrow
The graded doses of n-hexane extract of I. batatas-induced myeloid-erythroid cells with a mild increase of 20:40 (M: E ratio) for 125 mg/kg, 21.7:43.4 (M: E ratio) for 250 mg/kg and 23.3:46.6 (M: E ratio) for 500 mg/kg at day 14, when compared with distilled water alone, up to 25: 50 (M: E ratio) which is normal, and less than 14.9: 25.1 (M: E ratio) for 40 mg/kg phenylhydrazine group showing a severe anaemic condition in rats and 5 mg/kg of ferrous (iii) hydroxide-induced myeloid–erythroid ratio, all at day 14 (Fig. 9).
3.4 Acute and subacute study
The results from the experimental acute toxicity studies revealed that n-hexane leaf extracts were safe up to the highest dose of 5000 mg/kg. No lethal signs and symptoms or behavioural changes were observed. Also, no mortality was recorded during the period of the study.
The histological examination of the study showed that administration of graded doses of n-hexane leaf extract of I. batatas-induced moderate vascular dilation of the heart compared to graded doses of administered control (distilled water). The study also showed that administration of graded doses of n-hexane extract of I. batatas-induced mild vascular congestion and moderate Kupffer cell activation to the liver while control (distilled water) (Fig. 10).
The effect from n-hexane leaf extract of I. batatas on the spleen (Fig. 11) showed that administration of graded doses of n-Hexane extract of I. batatas induced normal follicular architecture on the spleen when compared with the Control (distilled water). The effect of n-hexane leaf extract of I. batatas on the spleen, as shown in Fig. 12, displayed graded doses of the treatment groups' induced normal follicular architecture of the spleen compared to the Control (distilled water). Poly-maltose induced severe sinus dilation and mild follicular atrophy on the spleen.
Figure 13 depicts the effect of n-hexane leaf extract of I. batatas on the kidneys. It showed that the treated groups induced mild interstitial congestion in the kidney compared with the control (distilled water).
The result also showed that Ipomoea batatas L. n-hexane leaf extracts displayed scavenging activities at 39.21 ± 1.70% at 100 µg/ml when compared with the standard (ascorbic acid) 89.02 ± 2.21. The scavenging property of the extract was more pronounced at the highest concentration, as shown in Fig. 1. The plant extract inhibits oxidation of DPPH, which indicates that it can donate protons and scavenge other stable radicals, given that phenylhydrazine-induced haemolysis could be a result of oxidative stress [15,16,17].
The study evaluated the anti-anaemic activity of n-hexane leaf extract of I. batatas on 40 mg/kg phenylhydrazine hydrochloride-induced haemolytic anaemia albino rats. The result of this study showed that haemolytic anaemia was caused using phenylhydrazine hydrochloride  intraperitoneally in albino rats, and I. batatas extract was orally administered to examine its result when compared with ferrous (iii) hydroxide (reference drug). The effect of the treated groups was observed by evaluating the haematological index, namely Hgb, HCT, RBC, MCHC, MCV and MCH, as shown in Figs. 2, 3, 4, 5, 6, 7. The result showed that exposure to phenylhydrazine hydrochloride reduced haemoglobin levels in untreated rats (Figs. 4 and 6). Anaemia was treated on days 1, 7 and 14 using ferrous (iii) hydroxide and I. batatas n-hexane extract. A similar effect was achieved by Ogwumike  anti-anaemia effects of Sorghum bicolor. Also, 125, 250, and 500 mg/kg of the extract stimulated haemoglobin production and ferrous (iii) hydroxide at day 14. Results from Figs. 2, 3, 4, 5, 6, 7 elicited the effect of n-hexane extract, triggered regeneration of red blood cell, haematocrit, haemoglobin, mean corpuscular volume and mean corpuscular haemoglobin, which is one of the significant markers that depicted anaemia. Specifically, at 250 and 500 mg/kg of the extracts it showed a better haematinic activity when compared with the anaemia group. This suggested the possible mechanism of action through which the extracts elicit its action, mimicking one of the actions displayed by iron ingestion. This agreed that haemoglobin is found in red blood cells; thereby, the effect from the extract improved their regenerations.
Additionally, it was also observed that there was a significant reduction in red blood cell count in the untreated group (haemolysis). This reduction recompensed the standard value in the treated groups by ferrous (iii) hydroxide and I. batatas extract. A similar result was acquired with the leave extract of Tectona grandis in Togo , Justicia secunda Vahl in Benin  and I. batatas . The non-anaemic group showed a slight increase in the mean number of red blood cells as observed.
Furthermore, the mean corpuscular haemoglobin concentration (MCHC) and mean corpuscular volume (MCV) were constants for typing anaemia. MCV reduction showed a significant difference in the untreated group after the administration of phenylhydrazine, signifying microcytosis. This reduction was counteracted at day 14 across the treated groups and day 14 in the untreated anaemic group.
Besides, the compensation was faster with ferrous (iii) hydroxide and I. batatas extract, implying to possible similar mechanisms implicated in erythropoiesis. This result varied with Ogwumike  studies in Nigeria who reported a reduction in the MCV when treated with an aqueous extract of Sorghum bicolor leaves. Augmentation of MCV divulges the release of enlarging premature erythrocytes (macrocytes) . However, an increase in MCHC repeals the comparability of MCV across experimental groups. Reduced MCHC was also reported by Ogwumike  in his experimental model. This decrease in MCHC reproduced red cells discharge and less haemoglobin inundated (hypochromic). It perhaps could be triggered by the release from macrocytes. This, therefore, indicated that I. batatas extract just as ferrous (iii) hydroxide improves the quantity of juvenile cells in blood swiftly due to subsequent triggers from haematopoiesis and their immature release into bloodstream preceding to the end of their differentiation [Figs. 2, 3, 4, 5, 6, 7]. Another study discovered improved osmotic red blood cells resistance with Justicia secunda Vahl extracts in Benin  and Tectona grandis in Togo . The extract displayed no consequence on the thrombocyte lineage via an exhibition of its effects not widen across all haematopoietic heredity.
The results of the study also showed that bone marrow of the treated groups has stimulating effects on the myeloid/erythroid ratio (20: 40, 21.7: 43.4 and 23. 3:46.6) when compared with the untreated group at 15.0: 25.0 and 25: 50 (M: E ratio), while normal control bone marrow, which could be liable for red blood cells stimulation in bone marrow, was considerable [Fig. 8]. Improvement in myeloid–erythroid cells ratio was observed in more in 500 mg/kg n-hexane extract. These findings agreed with the earlier study by Nostro et al., ; Noda et al.; Bratosin et al. on the significant alteration and increase in red blood cells morphology and myeloid–erythroid cells of the bone marrow. The finding enhances the property of the plant extract in the synthesis of normal red blood cells , and the mechanism of action could be triggered by the function of erythropoietin cells in the kidney to promote bone marrow myeloid–erythroid cells production of red blood cells .
No significant increase in the acute toxicological adverse effect, which could perhaps be endorsed for the acute toxicity of n-hexane extract of Ipomoea batatas L., was observed [Tables 1 and 2]. Moreover, negative behavioural changes were the significant observations showed in clinical physical signs . Our study did not observe any notable changes. It is remarkable to note that in the duration of the study, there was no mortality recorded. Therefore, it is suggested that a higher lethal dose (LD50) of n-hexane extract that was greater than 500 mg/kg can be administered since no death was observed from the doses administered, as shown in Table 1. These findings are absent with earlier studies  that reported no death at higher doses. More so, the administration of I. batatas leaf extracts showed no significant alteration in the body weights of the affected rats (Table 2), thereby suggesting no adverse effect on the metabolic actions of treated rats with the plant extract.
Similarly, no significant difference in tissue histology of rats in treated and control groups (P > 0.05) was observed. Implications from these results show that n-hexane extracts of sweet potatoes showed no toxicity as observed from the safety doses (125 mg – 500 mg/kg body weight). Sweet potato leaf extract in this study  may be attributed to fewer leaf options as medicinal benefits of I. batatas. Conversely, further and advanced studies will be desirable to suitably review the toxicity of I. batatas products with chronic toxicity studies.
In conclusion, the study showed that leaf extracts of Ipomoea batatas L. possess antioxidative, anti-anaemic properties and is safe even at higher doses at 500 mg/kg. Our study also provides the fundamental preclinical order of sequence in drug development related to anti-anaemic and antioxidative herbal therapy in Nigeria.
Availability of data and materials
Data were obtained from this research study and statistically analysed as shown in Tables and Figures Materials such as chemicals, drugs, kits and animals where ordered from necessary stores within and out the country.
Red blood cells
Mean corpuscular volume
Mean corpuscular haemoglobin
Mean corpuscular haemoglobin concentration
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Our sincere and deep appreciation goes to Mr. Dialect and Mr. Ehigie of the Department of Haematology University of Benin Teaching Hospital, Mr. Odega Kelvin and Mrs. Queen Okoro of the Department of Morbid Anatomy, University of Benin Teaching Hospital, and they did slides preparation and interpretation.
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All procedures using animals obtained the approval of Life Sciences Institutional Animal Ethical Committee, University of Benin with LS17101 ethical number.
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Gabriel, B.O., Idu, M. Antioxidant property, haematinic and biosafety effect of Ipomoea batatas lam. leaf extract in animal model. Beni-Suef Univ J Basic Appl Sci 10, 75 (2021). https://doi.org/10.1186/s43088-021-00161-4
- Ipomoea batatas L.
- Phenylhydrazine hydrochloride
- In vitro antioxidant