Antioxidant activity, acetylcholinesterase inhibitory potential and phytochemical analysis of Sarcocephalus latifolius Sm. bark used in traditional medicine in Sudan

Abstract

Background

Sarcocephalus latifolius is used as a traditional medicine for curing many diseases in Sudan. The main objective of the current study was to determine the antioxidant activity and acetylcholinesterase inhibition (AChEI) of S. latifolius, and to estimate its total phenolic and flavonoid contents.

Methods

Antioxidant activity of the tested plant extracts was carried out by determining their ability to scavenge the 2,2-diphenyl-1-picryl hydrazyl (DPPH) free radical. On the other hand, AChE inhibitory activity was determined spectrophotometrically using the Ellman’s colorimetric method. The levels of total phenols and flavonoids were determined quantitatively using spectrophotometric methods. MTT assay was consumed to assess the cytotoxic effect of the most active fractions. These fractions were subjected to phytochemical analysis using GC-MS techniques to determine thier chemical composition.

Results

Hexane and chloroform fractions exhibited the highest antioxidant activity with IC₅₀ values of (0.098 ± 0.08 and 0.099 ± 0.029 mg/ml) respectively. Standard propyl gallate had the lowest IC₅₀ value of 0.0414 ± 0.11 mg/ml. The ethanolic crude extract showed low AChEI activity with 40.2 ± 0.10%. High concentrations of phenolic and flavonoid contents were observed. GCMS revealed the presence of well-known antioxidants compounds e.g. Vitamin E and caffeic acid.

Conclusion

The ethanolic extract of bark of S. latifolius showed potent antioxidant effects and low AChEI activity, high phenolic and flavonoid contents and presence of pharmacologically active compounds. These findings explain its wide usages in traditional medicine.

Background

Due to its high reactivity, Oxygen is capable of becoming part of potentially damaging molecules called reactive oxygen species (ROS) [1]. Humans have evolved a highly sophisticated antioxidant protective system, both endogenous and exogenous in origin [2]. Whenever the balance between ROS production and antioxidant effect is disturbed, ‘oxidative stress’ results leading to various pathological conditions [3]. Many researchers have focused on antioxidant activity of phenolic compounds especially flavonoids and a positive correlation was observed [4–6]. ROS are playing a dangerous role in the pathogenesis of various diseases, including neurodegenerative disorders, cancer and artherosclerosis [7, 8]. Oxidative processes are the pathogens associated with the central nervous system in Alzheimer’s disease (AD). The brain in particular is highly vulnerable to oxidative damage as it consumes about 20% of the body’s total oxygen, with a high content of polyunsaturated fatty acids and lower levels of endogenous antioxidants [9, 10]. The brain of patients suffering from AD is said to be under oxidative stress. [11, 12]. AD is the most common neurodegenerative disorder, characterized clinically by progressive memory deficits and impaired cognitive function [13]. It is a major public health concern due to the increasing number of sufferers, placing strains on caregivers as well as on financial resources [14]. A deficiency in levels of the neurotransmitter acetylcholine (ACh) has been observed in the brains of AD patients, and inhibition of acetylcholinesterase (AChE), the key enzyme which hydrolyses ACh, is a major treatment option for AD [15]. Traditionally plants have been shown to be good options in the search for AChE inhibitors. Recently, several plants have been identified as containing AChEI activity [7]. In this respect, medicinal plants provide a rich source of biologically active constituents with multiple activities. Sarcocephalus latifolius Sm. (family: Rubiaceae), locally known as “Karmadoda”, have many uses in traditional medicine including malaria, dysentery, fever, hypertension and health promotion (antioxidant) [16–18].

Methods

Plant materials

Bark samples of S. latifolius were collected from South Kordfan state in February 2015. Identified and authenticated by Prof. Hatel H. Alkamali, Faculty of Science and Technology, Omdurman Islamic University, and confirmed by plant taxonomists at the herbarium of Medicinal and Aromatic Plants Research Institute, National Center for Research. Khartoum, Sudan.

Extraction

The fresh samples were dried in shade for seven days, pulverized then used for extraction. Cold maceration methodology was carried out according to published method of Osama and Awdelkarim, 2015 [19].

Fractionation

The crude extract was fractionated using liquid- liquid extraction methodology, which were carried by dissolving the samples in dist. H₂O then partitioned between n-hexane, chloroform, ethyl acetate and n-butanol respectively using separating funnel apparatus.

Qualitative phytochemical evaluation

Phytochemical screening was conducted to determine the presence of natural products in the fractions of selected plants using standard methods [20, 21].

Determination of total phenolic content

Total phenolic content was determined by Folin Ciocalteu method [22]. Calibration curve was constructed using gallic acid standards Fig. 1 and the total phenolic content was expressed as mg gallic acid equivalents (GAE)/g dry weight (DW).

Fig. 1.

Standard curves of (a) Gallic acid and (b) Quercetin shows the absorbance against concentration

Determination of flavonoid content

The flavonoid content was measured by the aluminium chloride colorimetric assay [23]. Calibration curve was plotted using quercetin standards and flavonoid content was expressed as mg quercetin equivalents (QE)/g DW.

GC-MS analysis

GC-MS analysis was carried out using GCMS instrument (Model GCMS-QP2010 Ultra, Shimadzu Co., Japan) equipped with a capillary column Rtx-5 (0.25 휇m film × 0.25 mm i.d. × 30 m length). The instrument was operated in electron impact mode at ionization voltage (70 eV), injector temperature (250 ^∘C), and detector temperature (280 ^∘C). The carrier gas used was helium (99.9% purity) at a flow rate of 1.2 mL/min and about one 휇L of the sample was injected. The oven temperature was initially programmed at 110 °C (7 min) to 200 °C at 10 °C/min and from 200 to 280 °C at 5 °C/min withhold time 0 and 9 min respectively. The identification of compounds from the spectral data was based on the available mass spectral records (NIST and WILEY libraries).

Antioxidant activity: 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay

The test samples were prepared in DMSO as 10× stocks from each test concentration (between 0 and 100 μg/ml) and briefly sonicated when necessary in an ultrasonic water bath. Solvents fractions producing radical scavenging activities equal to or higher than 50% at 100 μg/mL in a preliminary screen were further tested and IC₅₀ (concentration of the sample producing 50% scavenging of DPPH radicals) determined using EZ-Fit Enzyme Kinetic Program. propyl gallate was tested in the assay as positive control. The assay method used in the present study was based on Shimada et al., 1992 [24] method. The samples stock solutions (20 μL/well) were dispensed in triplicate onto 96-well plates. The assay was started with the addition of DPPH reagent (300 μM in ethanol, 180 μL/well). Appropriate blanks were prepared using the solvent only in addition to the same amount of DPPH reagent to get rid of any inherent solvent activity. Negative controls were also run in parallel to correct for any non-DPPH absorbance by coloured extracts at the test wavelength. The plate was immediately shaken for 30 s and incubated in the dark for 30 min at room temperature. The remaining DPPH was measured in the microplate reader at 517 nm. Percentage of radical scavenging activity (RSA) was calculated as following:

$$\%\mathrm{RSA}=100-\left\{\left(\mathrm{Ac}-\mathrm{At}\right)/\mathrm{Ac}\right\}\times 100$$

Where, At = Absorbance value of test compound; Ac = Absorbance value of control.

The multi-well plate AChE inhibition assay

The AChE inhibitory activity was tested using 96 well micro-plate assay based on Ellmam et al., 1961 [25] method with minor modifications. Each extract (10 μL of 5 mg/mL in ethanol) was dispensed in triplicate onto 96 well microplate and mixed with 190 μL of Ellman’s mixture containing 20 μL of enzyme, 140 μL to phosphate buffer, pH 8, containing 10 μL of 0.5 mM of 5, 5’- dithio-bis-(2-nitrobenzoic acid) (DTNB, Sigma-Aldrich, Germany) and 20 μL acetylthiocholine iodide (ATCI, Sigma-Aldrich, Germany). The control wells contained ethanol instead of the extract. The enzymatic activity was monitored at 412 nm every 30 s intervals for 3 min (linear reaction). The enzyme rate was calculated from the slope of the curve of absorbance vs time. As screening strategy, final concentration of 1000 μg/mL from each extract was examined and the average % inhibition was calculated relative to the enzyme rate at the control wells according to the following equation:

$$\%\text{Inhibition}=100-\left\{\left(\mathrm{Ac}-\mathrm{At}\right)/\mathrm{Ac}\right\}\times 100$$

MTT (3-(4, 5-dimethylthazol-2-yl)-2, 5-diphenyl tetrazonium bromide) cytotoxicity assay

In the present investigation, Vero (normal, African green monkey kidney) cell line was used and cytotoxicity on these cells was assessed as described previously [26]. For each experiment, cultures were seeded from frozen stocks. Vero cells were maintained complete medium consisting of 10% fetal bovine serum and 90% minimal essential medium (MEM). The cells were incubated at 37 °C in a 5% CO₂ atmosphere and were in the logarithmic phase of growth at the time of the neutral red (NR) and tetrazolium (MTT) assays. Cells were harvested and seeded into 96-well tissue culture plates at a density of 1 × 10⁴ cells per well of aliquots of medium (200 μL). The cells were allowed to adhere to the wells for 24 h at 37 °C in a humid atmosphere optimized with 5% CO₂ in air. The next day, the plant fractions were added at the desired final concentrations and incubated for 72 h. All experiments were performed at least four times. Phosphate-buffered saline (PBS) was used as a negative. After the 72 h exposure period, the toxic endpoints were determined at 570 nm. Viability was defined as the ratio (expressed as a percentage) of absorbance of treated cells to untreated cells that served as negative control.

Statistical analysis

All data were expressed as means ± SD for three experiments. P values <0.05 were considered statistically significant. Statistical analyses were performed using Excel software (Microsoft 2010).

Results and discussion

Extraction yield and phytochemical screening

The percentage yield of S. latifolius ethanolic extract was 47.33% of dry weight. The polar fractions (water and butanol) showed the highest percentage yield (Table 2), this could be attributed to the polar nature of the crude extract obtained with polar solvent (ethanol).

Table 2.

Yield percentages, Total phenolic and flavonoid contents of ethanolic extract and solvent fractions of S. latifolius

Sample	Extraction yield (w/w% of dry weight)	Phenolic content (mg /g GAE)	Total flavonoid (mg/g QE)
Crude	47.33	78.21 ± 2.4	91.36 ± 0.84
Hexane	6.18	98.78 ± 2.1	81.01 ± 0.012
CHCl3	1.64	71.49 ± 0.5	118.29 ± 0.21
EtOAc	3.09	86.12 ± 0.7	80.23 ± 0.03
BuOH	19.09	56.20 ± 1.23	94.32 ± 0.71
H2O	70.91	83.20 ± 3.7	40.22 ± 0.28

The results of preliminary investigation on the phytochemicals present in different solvent fractions are presented in Table 1. Different phytoconstituents such as phenolics, flavonoids, tannins, alkaloids, saponins, quinones, steroids, and terpenoids were detected in the tested fractions. The phytochemicals investigated in the present study are known to be beneficial in industrial and medicinal sciences [27]. Also, this preliminary knowledge can be looked at as a decipher in the search of a new source of economically valued chemical compounds [28, 29].

Table 1.

Preliminary screening of secondary metabolites in the fractions of S. latifolius

Family of compound	Type of test	interference
		n-hexane	CHCl3	EtOAc	n-BuOH	H2O
Phenols	FeCl3	+v	+v	+v	+v	+v
Tannins	FeCl3	-v	+v	+v	+v	+v
Flavonoids	KOH	+v	+v	+v	+v	+v
	Alkaline	+v	+v	+v	+v	+v
	Lead acetate	+v	+v	+v	+v	+v
Quinones	H2SO4	-v	+v	+v	+v	+v
Alkaloids	Dragendorff’s	+v	+v	+v	+v	+v
	Wagner’s	+v	+v	+v	+v	+v
Triterpenes	Salkowski	+v	+v	+v	+v	+v
Diterpenes	Copper acetate	-v	-v	-v	-v	-v
Steroids	Salkowski	+v	+v	+v	+v	+v
Saponins	Forth	-v	+v	+v	-v	+v

+ve positive -ve negative

Total phenolic and flavonoid contents

Crude natural extracts and compounds purified from these extracts can serve as better herbal drug sources owing to their fewer side effects and nutritional value [30]. As presented in Table 2, the ethanolic crude extract of S. latifolius bark exhibited total phenolic content of 78.21 ± 2.4 mg GAE/g DW. Fig. 2 a similar study carried out using the methanolic leaf and root extracts of S. latifolius, has shown that the total phenolic content present was (0.016 ± 0.03 and 0.036 ± 0.05 mg GAE/g DW) respectively, which is very low compared to the present study [31]. This high variation could be due to many reasons including, the part of plant under study, which contains different chemical composition with different percentage, the method, solvent used for extraction, the origin of plant samples, and the environmental factors. The hexane fraction showed the highest phenolic content (98.78 ± 2.1 mg GAE/g DW), this result indicates the presence of high lipid soluble phenolic compounds such as vitamin E, whose existence was confirmed by GCMS analysis.

Fig. 2.

Comparison charts of (a) Total phenolic content. b Total flavonoid content of ethanolic extract and solvent fractions of S. latifolius

Successful determination of biologically active compounds from plant material is largely dependent on the type of solvent used in the extraction procedure. Higher concentrations of more bioactive flavonoid compounds were detected with 80% ethanol [32]. Therefore, ethanol was chosen for extraction. Plant phenolic compounds especially flavonoids are currently receiving greater interest due to their antioxidants potential [27, 33]. Aluminium chloride colorimetric assay yielded total flavonoid content of (91.36 ± 0.84 mg QE/g DW) for the crude extract. Highest flavonoid contents were observed in chloroform fraction (118.29 ± 0.21 mg QE/g DW), which indicate the high amount of less polar flavonoids (aglycones) such as isoflavones, flavanones, highly methoxylated flavones, and flavonols [34]. These results could give a clue interpreting the observed high bioactivities of this plant.

Antioxidant and AChE inhibitory activities

Recently, interest has increased in naturally occurring antioxidants that can be used to protect human beings from oxidative stress damages [35, 36]. In the current study, the ethanolic crude extract exhibited high antioxidant activity with 87 ± 0.03%. The order of the activity (IC₅₀ mg/ml) was as follow: hexane (0.098 ± 0.08) > chloroform (0.099 ± 0.029) > butanol (0.104 ± 0.19) > ethyl acetate (0.148 ± 0.33) and eventually water fraction (2.015 ± 0.3), Table 3 and Figs. 3, and 4 illustrate these results. The activity of hexane and chloroform fractions (0.098 ± 0.08 and 0.099 ± 0.029 mg/ml) respectively, is comparable values to the standard antioxidant PG (0.0414 ± 0.11 mg/ml); they also showed high amount of phenolic and flavonoid contents, it’s possible that could be the reason of this high antioxidant potential.

Table 3.

Antioxidant activity (%RSA and IC₅₀) of solvent fractions of S. latifolius

Sample	% RSA	IC50 (mg/ml)
Hexane	76 ± 0.02	0.098 ± 0.08
CHCl3	86 ± 0.03	0.099 ± 0.029
EtOAc	84 ± 0.03	0.148 ± 0.33
BuOH	83 ± 0.02	0.104 ± 0.19
H2O	79 ± 0.10	2.015 ± 0.3

Fig. 3.

Percentage of RSA of S. latifolius ehanolic extract and solvent fractions

Fig. 4.

Comparison Chart of Antioxidant potentials of S. latifolius fractions with the decrease of concentration (IC50 evaluation)

Inhibition of AChE has been considered as a promising strategy for the treatment of neurological disorders such as Alzheimer’s disease, senile dementia, ataxia and myasthenia gravis, in which a deficit in cholinergic neurotransmission is involved [37, 38]. The side effects of anti-AChE drugs such as toxicity, tolerability, and loss of efficiency stimulates the researchers to screen alternative natural anti-AD drugs for medication switch [39]. Ethanolic extract displayed low AChE inhibitory activity with (40.2 ± 0.10). GCMS analysis of chloroform fraction indicates the presence of caffeic acid which has been reported to be a potent inhibitor of both AChE and BChE [40]. It is possible that the solvent used for extraction was not able to isolate the active ingredients with a proper amount.

GCMS analysis

Due to their superior antioxidant activities hexane and chloroform fractions were analyzed with GC-MS, to identify their chemical composition which may be responsible of the measured activities. The GC-MS analysis lead to the identification of a number of compounds. These compounds were identified through mass spectrometry attached with GC. Interpretation of mass spectrum was conducted using the database of National Institute Standard and Technology (NIST). The name, molecular weight and structure of the components of the test materials were ascertained, illustrated in Tables 4, and 5 and Figs. 5, and 6.

Table 4.

GC-MS spectral analysis of hexane fraction of S. latifolius bark

Peak no.	R. Time	Area %	Compunde name	Molecular Formula	Mass
1	13.736	1.68	5,5-Dimethyl-1,5-oxasilonan-9-one	C9H18O2Si	186
2	15.467	5.67	Quinic acid	C7 H12 O6	192
3	19.188	0.29	Pentadecanoic acid, methyl ester	C16 H32 O2	256
4	19.425	0.67	Ethyl (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate	C12H14O4	222
5	19.805	6.89	Pentadecanoic acid	C15H30O2	242
6	20.147	2.20	Palmitic acid ethyl ester	C18 H36 O2	284
7	20.761	0.53	2-Cyclopropylideneadamantane	C13H18	174
8	22.455	16.49	Oleic Acid	C18H34O2	282
9	22.694	3.23	Methyl linoleate	C19 H34 O2	294
10	22.765	1.64	Ethyl octadec-9-enoate	C20H38O2	310
11	22.814	0.48	Linolenic acid methyl ester	C19 H32 O2	292
12	23.122	3.91	Heptadecanoic acid, ethyl ester	C19 H38 O2	298
13	25.920	14.21	Oelic acid amide	C18 H35 N O	281
14	25.994	0.23	Oelic acid amide	C18 H35 N O	281
15	26.187	0.44	Palmitic acid ethyl ester	C18 H36 O2	284
16	26.265	0.60	Stearic acid amide	C18H37NO	283
17	26.509	0.43	2-Pentyl-2-nonenal	C14H26O	210
18	26.761	0.43	Oxirane, hexadecyl-	C18H36O	268
19	28.299	0.48	Octadecanal	C18H36O	268
20	28.665	9.23	Phthalic acid, mono-(2-ethylhexyl) ester	C16H22O4	278
21	29.192	0.97	Ethyl palmitate	C18 H36 O2	284
22	29.881	19.50	Cinchol	C29 H50 O	414
23	32.086	0.57	Ethyl docosanoate	C24H48O2	368
24	32.642	1.64	Spinacene	C30H50	410
25	33.176	0.59	3-[(Trimethylsilyl)oxy]lanosta-8,24-diene	C33H58OSi	498
26	33.343	1.44	Lupenyl acetate	C32H52O2	468
27	35.907	3.46	Stigmast-4-en-3-one	C29H48O	412
28	38.248	1.09	Cholesteryl bromide	C27 H45 Br	448
29	38.974	1.01	Vitamin E	C29H50O2	430

Table 5.

GC-MS spectral analysis of chloroform fraction of S. latifolius bark

Number	R. Time	Area %	Compound name	Molecular Formula	Mass
1	13.735	2.97	5,5-Dimethyl-1-oxa-5-silacyclononanone-9	C9H18O2Si	186
2	14.635	0.29	9-Eicosene, (E)-	C20H40	280
3	15.989	1.99	2H–Pyran-2-one, 5-ethylidenetetrahydro-4-(2-hydroxyethyl)-	C9H14O3	170
4	17.029	0.85	4-((1E)-3-Hydroxy-1-propenyl)-2-methoxyphenol	C10H12O3	180
5	17.334	0.35	1-Heptadecene	C17H34	238
6	18.302	0.84	p-Hydroxycinnamic acid, ethyl ester	C11H12O3	192
7	19.187	0.35	9-Octadecenoic acid, 12-(acetyloxy)-, methyl ester, [R-(Z)]-	C21H38O4	354
8	19.361	0.18	7,9-Di-tert-butyl-1-oxaspiro(4,5)deca-6,9-diene-2,8-dione	C17H24O3	276
9	19.422	0.15	alpha.-D-Xylofuranose, 1,2-O-isopropylidene-5-(t-butyldimethylsilyl)-	C14H28O5Si	304
10	19.800	5.89	Pentadecanoic acid	C15 H30 O2	242
11	20.115	0.30	9-Tricosene, (Z)-	C23H46	322
12	20.360	7.84	2H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy-	C10 H8 O4	192
13	20.761	0.62	Bicylo[4.1.0]heptane, 7-bicyclo[4.1.0]hept-7-ylidene-	C14H20	188
14	21.139	0.22	Trimethylsilyl 3-methoxy-4-(trimethylsilyloxy)cinnamate	C16H26O4Si2	338
15	21.769	0.31	9-Octadecenoic acid (Z)-, methyl ester	C19H36O2	296
16	21.996	25.46	2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-	C9 H8 O4	180
17	22.450	9.78	Oleic Acid	C18H34O2	282
18	22.762	3.28	Octadecanoic acid	C18H36O2	284
19	23.104	1.19	1-Hexadecene	C16 H32	224
20	23.740	0.61	9,12-Octadecadienoic acid (Z,Z)-	C18H32O2	280
21	25.816	0.39	O O′-BIPHENOL, 4,4’,6,6’-TETRA-T-BUTYL-	C28 H42 O2	410
22	25.909	1.08	9-Octadecenamide, (Z)-	C18 H35 N O	281
23	26.155	0.93	1-Nonadecene	C19H38	266
24	28.301	0.19	Oxirane, heptadecyl-	C19H38O	282
25	28.662	1.17	1,2-Benzenedicarboxylic acid, mono(2-ethylhexyl) ester	C16H22O4	278
26	29.163	1.28	1-Nonadecene	C19H38	266
27	29.732	1.15	gamma.-Sitosterol	C29H50O	414
28	32.053	1.83	1-Triacontanol	C24H50O	354
29	35.350	1.02	17-Pentatriacontene	C35H70	490
30	35.848	5.09	Methyl commate C	C31 H50 O4	486
31	38.123	22.40	Lup-20 (29)-en-3-ol, acetate, (3.beta.)-	C32H52O2	468

Fig. 5.

GC-MS chromatogram for hexane fraction of S. latifolius bark

Fig. 6.

GC-MS chromatogram for chloroform fraction of S. latifolius bark

GC-MS spectrum of the hexane and chloroform fractions revealed the presence of 29 and 31 compounds respectively. Two phenolic compounds (Ethyl (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate and Vitamin E) were observed in hexane fraction. Fat soluble vitamin E is one of the most active natural antioxidants, it is the most effective chain-breaking antioxidant within the cell membrane where it protects membrane fatty acids from lipid peroxidation. The supplemental intakes of this powerful antioxidant have been documented to be useful against cancer [41]. Vitamin E also acts in the prevention of free radical formation.

chloroform fraction declared the presence of five phenolic substances (4-((1E)-3-Hydroxy-1-propenyl)-2-methoxyphenol; p-Hydroxycinnamic acid, ethyl ester; 2H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy; Caffeic acid, O O’-biphenol, 4,4’,6,6’-tetra-T-butyl) these phenolic compounds are known antioxidants, therefore the antioxidant potentials of this plant could be justified. However, further studies on the isolation, characterization, and biological evaluation of these identified compounds are necessary to confirm their potential benefits.

Cytotoxicity study

MTT assay reveled that, all tested fractions have no toxic effects on Vero cells with IC₅₀ more than 200 μg/ml, these results are shown in (Table 6).

Table 6.

The cytotoxic effect (expressed as % inhibition and IC50 values) of hexane and chloroform fractions of S. latifolius tested at 125, 250 and 500 μg/ml against Vero cells

Code of extract	Concentration (μg/ml)			IC50 (μg/ml)	IC50
	Inhibition % ± SD
	500	250	125
Hexane	55.3 ± 0.04	50.4 ± 0.02	40.9 ± 0.03	277.8	>100
Chloroform	67.6 ± 0.08	55.0 ± 0.01	35.9 ± 0.05	224.9	>100
Control	95.3 ± 0.00				<30

IC₅₀ < 30 μg/ml: High toxic. Control = triton was used as positive control at 0.2 μg/ml. the maximum concentration used was 500 μg/ml

The MTT assay is a test of metabolic competence based upon assessment of mitochondrial performance relying on the conversion of yellow MTT to the purple formazan derivative by mitochondrial succinate dehydrogenase in viable cells [42]. Increasing concentrations of the tested fractions did not affect mitochondrial respiration as measured by the MTT cytotoxicity assay. However, the results of this assay measuring cell integrity showed that these solvent fractions are not toxic over this concentration range tested.

Conclusion

S. latifolius is a Sudanese medicinal plants commonly used as herbal medicine for several purposes. In the present study, the selected plant was investigated in vitro for AChEI and antioxidant properties. In addition, the total phenolic and flavonoids contents were measured. GC-MS analysis of S. latifolius (hexane and chloroform) fractions reveled the presence of well known antioxidant compound such as Vitamin E and Caffeic acid. According to these findings it could be suggested that S. latifolius (hexane and chloroform) fractions might be potent and safe antioxidant materials in medicine or food industry.

Abbreviations

Abs

Absorbance

Ac

Absorbance value of Control

Ach

Acetylcholine

AChE

Acetylcholinesterase

AChEI

Acetylcholinesterase Inhibitory

AD

Alzheimer’s Disease

At

Absorbance value of Test compound

BuOH

Butanol

DMSO

Dimethyl sulfoxide

DPPH

2,2-diphenyl-1-picryl hydrazyl

DTNB

5,5’-Dithiobs (2-nitro benzoic acid)

EI

Electron Ionization

EtOAc

Ethyl Acetate

FBS

Fetal Bovine Serum

GAE

Gallic Acid Equivalent

GC

Gas Chromatography

GC-MS

Gas Chromatography- Mass Spectrometer

MEM

Minimal Essential Medium

MTT

Microculture tetrazolium

NIST

National Institute of Standards and Technology

PG

Propyl Gallate

QE

Quercetin Equivalent

RSA

Radical Scavenging Activity