Advances in Pharmacological and Pharmaceutical Sciences

Advances in Pharmacological and Pharmaceutical Sciences / 2016 / Article

Research Article | Open Access

Volume 2016 |Article ID 3720850 |

Urmeela Taukoorah, M. Fawzi Mahomoodally, "Crude Aloe vera Gel Shows Antioxidant Propensities and Inhibits Pancreatic Lipase and Glucose Movement In Vitro", Advances in Pharmacological and Pharmaceutical Sciences, vol. 2016, Article ID 3720850, 9 pages, 2016.

Crude Aloe vera Gel Shows Antioxidant Propensities and Inhibits Pancreatic Lipase and Glucose Movement In Vitro

Academic Editor: Robert Gogal
Received30 Sep 2015
Revised10 Nov 2015
Accepted09 Dec 2015
Published04 Jan 2016


Aloe vera gel (AVG) is traditionally used in the management of diabetes, obesity, and infectious diseases. The present study aimed to investigate the inhibitory potential of AVG against α-amylase, α-glucosidase, and pancreatic lipase activity in vitro. Enzyme kinetic studies using Michaelis-Menten () and Lineweaver-Burk equations were used to establish the type of inhibition. The antioxidant capacity of AVG was evaluated for its ferric reducing power, 2-diphenyl-2-picrylhydrazyl hydrate scavenging ability, nitric oxide scavenging power, and xanthine oxidase inhibitory activity. The glucose entrapment ability, antimicrobial activity, and total phenolic, flavonoid, tannin, and anthocyanin content were also determined. AVG showed a significantly higher percentage inhibition () of pancreatic lipase compared to Orlistat. AVG was found to increase the Michaelis-Menten constant and decreased the maximal velocity () of lipase, indicating mixed inhibition. AVG considerably inhibits glucose movement across dialysis tubes and was comparable to Arabic gum. AVG was ineffective against the tested microorganisms. Total phenolic and flavonoid contents were  (GAE)/mg and  (RE)/mg, respectively. AVG also showed interesting antioxidant properties. The biological activity observed in this study tends to validate some of the traditional claims of AVG as a functional food.

1. Introduction

Aloe vera is one of nature’s most sacred therapeutic medicinal food plants. The medicinal potential of this tropical succulent has urged recurrent myths about its properties that have persisted from the fourth century BC throughout world history [1]. There are also reports that tend to show that Alexander the Great used Aloe vera to treat his wounded soldiers and Cleopatra used it for skin care [2]. Over the years, this exquisite plant has acquired names such as “the wand of heaven,” “heaven’s blessing,” and “the silent healer” [3]. Native to Northern Africa, this plant has been in existence for over 2000 years [2].

Parenchymatous gel from Aloe vera leaves is extensively used in folk medicine, health drinks, topical creams, toiletries, and cosmetics [4]. Without any doubt, the commercialisation of Aloe vera is a success story. Various kinds of natural-based industries have a share in the Aloe vera market, most notably the cosmetic, food, beverage, and dietary supplement industries. The major constituents of Aloe vera gel can be classified into five groups, namely, phenolics, saccharides, vitamins, enzymes, and low molecular weight substances [5]. Aloe vera gel has an assortment of pharmacological properties which encompasses antiviral, antibacterial, laxative, protection against radiation, antioxidant, anti-inflammation, anticancer, antidiabetic, antiallergic, and immunostimulation properties amongst others [5, 6].

Apart from skin disorders, Aloe vera gel can also be also applied on superficial or partial thickness burns to fasten healing process and reduce pain [7, 8]. It helps in soothing skin injuries affected by burning, skin irritations, cuts, and insect bites. Faster wound closure has also been demonstrated in rats treated with isolated and characterised Aloe vera polysaccharides [9]. Aloe vera further reduces inflammation by downregulating proinflammatory cytokine production in activated human macrophages and thus interfering with the cytokine overproduction during early sepsis or in chronic inflammatory or autoimmune disease, thereby ameliorating the outcome and quality of life of patients [10]. Aloe vera polysaccharides have also been speculated to enhance immunity activity and exert antioxidant effects in oral ulcer animal models [11].

Furthermore, Aloe vera has shown its potential in the management of diabetes mellitus (DM). Clinical trials have shown that, in obese individuals with prediabetes or early untreated diabetes mellitus, Aloe vera gel complex reduced body weight, body fat mass, and insulin resistance [12]. Abo-Youssef and Messiha (2013) also proved the antidiabetic effect of Aloe vera leaf pulp extract in vivo and in vitro as compared to glimepiride [1316].

Despite the availability of panoply of information on Aloe vera, there is insufficient scientific evidence on the efficacy of untreated or unprocessed local cultivar of Mauritian Aloe vera gel and its mechanism of action. Additional work is required to probe into the antidiabetic, antimicrobial, and antioxidant properties of the Mauritian Aloe vera gel which may help to validate its traditional claims. This endeavour will also delineate further health benefits of A. vera so as to encourage its use as a herbal medicine or functional food. Therefore, the main aim of this in vitro study was to investigate the antidiabetic, antimicrobial, and antioxidant activities of crude Aloe vera gel.

2. Methodology

2.1. Plant Material

Fresh Aloe vera leaves (Figure 1) were collected from Vacoas in October 2013. They were authenticated and an identification code (UTAV201301) was assigned to the specimen.

2.2. Preparation of Plant Material

The leaves were washed thoroughly under running tap water and then patted dry using clean filter papers. The peels were discarded while the gel was finely crushed using an electric blender. The resulting gel paste was used in all the tests.

2.3. Alpha-Amylase Inhibition Assay

The activity of α-amylase was carried out according to the method of Mao and Kinsella [17], based on the starch-iodine colour changes with minor modifications. Soluble starch solution (1%) was used as substrate. The starch solution was prepared by adding 1 g of soluble potato starch in 10 mL water and then boiled for 2 minutes. After cooling, water was added to reach a final volume of 100 mL. α-amylase solution (0.1 mL of 15 μg/mL in 0.1 M acetate buffer at pH 7.2 containing 0.0032 M sodium chloride) was added to a mixture of 3 mL of 1% soluble starch solution and 2 mL of acetate buffer (0.1 M, pH 7.2) preequilibrated at 30°C in a water bath. Substrate and α-amylase blank determinations were undertaken under the same conditions.

At zero time ( min) and at the end of the incubation period (), 0.1 mL of reaction mixture was withdrawn from each tube after mixing and transferred into 10 mL of an iodine solution (0.254 g iodine and 4.0 g potassium iodide in 1 litre). After mixing, the absorbance of the starch-iodine mixture was measured immediately at room temperature at 565 nm using a spectrophotometer. The absorbance of the starch blank was subtracted from the sample reading. One unit of amylase activity was arbitrarily defined as follows: , where and are absorbance of the iodine complex of the starch digest at zero time and after 60 minutes of hydrolysis. Specific activity of α-amylase was defined as units/mg protein/60 min. Percentage inhibition was calculated using the following equation:

2.4. Alpha-Glucosidase Inhibition Assay

Alpha-glucosidase inhibitory activity was performed following the modified method of Pistia-Brueggeman and Hollingsworth [18]. In test-tubes, a reaction mixture containing 500 μL of phosphate buffer (50 mM, pH 6.9), 100 μL of α-glucosidase (1 U/mL), and 200 μL of plant extract of varying concentrations was preincubated for 5 minutes at 37°C and then 200 μL of 1 mM PNPG (4-nitrophenyl-alpha-D-glucopyranoside) substrate was added to the mixture. After further incubation at 37°C for 30 minutes, the reaction was stopped by the addition of 500 μL of sodium carbonate (0.1 M). Enzyme, inhibitor, and substrate solutions were all prepared using the same buffer. Acarbose (5 mg/mL) was used as a positive control and water as a negative control. The yellow colour produced (due to p-nitrophenol formation) was quantitated by colorimetric analysis and reading the absorbance at 405 nm. Each experiment was performed in triplicate, along with appropriate blanks. The percentage inhibition was calculated using the formula

2.5. Porcine Pancreatic Lipase Inhibitory Assay

The porcine pancreatic lipase inhibitory assay was adapted from Zheng et al. and Bustanji et al. [19, 20]. Briefly, 50 μL of porcine pancreatic lipase (1 mg/mL) was added to a mixture containing 100 μL extract and 50 μL tris-HCl buffer (2.5 mM, pH 7). The resulting mixture is then incubated at 37°C for 15 minutes. After the incubation period, 100 μL of PNPB is then added to the test-tube. The mixture is again incubated for 1 h at 37°C. The absorbance is read at 405 nm. Percentage inhibition is calculated using the equation below:

2.6. Enzyme Kinetics Using Michaelis-Menten and Lineweaver-Burk Equations

The assay was adapted from Zheng et al. [19] and p-nitrophenol calibration curve was generated. The extract and porcine pancreatic lipase were mixed in a ratio of 2 : 1, respectively, and preincubated for 15 minutes. After 15 minutes, 150 μL of enzyme-extract mixture was added to each well containing 50 μL buffer and 100 μL PNPB of varying concentrations (with starting concentration 25.5 mM). The plate was then put in the incubator at 37°C for 30 minutes. After the incubation period, absorbance was determined at 405 nm. A double reciprocal plot using Michaelis-Menten and Lineweaver-Burk equations was generated.

2.7. Effect of Aloe vera Gel on In Vitro Glucose Movement

In vitro glucose diffusion studies were carried out by following the method with slight modifications described by Gallagher et al. and Edwards et al. [21, 22]. Briefly, the system consisted of a one-sided sealed dialysis tube (10 cm × 15 mm, dialysis tubing membrane, Sigma-Aldrich MW12173) into which 2 mL of 22 mM D-glucose in 0.15 M NaCl and 1 mL extract (50 g/L)/control (water) were incorporated. The other end was then sealed and the membrane was placed into a 100 mL glass beaker containing 40 mL 0.15 M NaCl and 10 mL distilled water to equilibrate the strength of internal and external medium. The beakers were placed into an orbital shaking incubator (JISICO) at 37°C at 100 rpm. The movement of the glucose into the external medium with respect to a negative control was monitored at set time intervals, that is, , , , , and 4 hrs. The absorbance was read at 500 nm. All tests were carried out in triplicate and glucose concentrations were measured using glucose oxidase kit method (GIBCO, Italy).

2.8. Antimicrobial Assay

The antibacterial and antifungal properties of the extracts were assessed by using modified antimicrobial assay utilising microtitre plate described by Drummond and Waigh [23]. Briefly, using aseptic techniques a single colony of microbe was transferred into a 100 mL bottle of peptone water broth, capped, and placed in incubator overnight at 35°C. After 12–18 h of incubation, using aseptic preparation and the aid of a centrifuge, a clean sample of microbe was prepared. To the sterile microtitre plates, 100 μL of peptone water broth is first added to all wells, followed by 100 μL of extract or control. Then, 100 μL of microbial culture was further added. The resulting mixtures were then left to incubate for 24 h at ambient temperature. After incubation, 40 μL INT (iodonitrotetrazolium) (0.2 mg/mL) was added to all the wells and left to incubate for a further 20 minutes. The microplates were then assessed visually to determine the minimum inhibitory concentration (MIC). Controls used for bacteria are Gentamicin, Chloramphenicol, and Streptomycin while controls used for fungi are Ampicillin and Amphotericin.

2.9. Ferric Reducing Antioxidant Power (FRAP) Assay

The ability of the extracts to reduce iron was determined according to the modified method of Benzie and Strain [24] where Trolox was used as standard. Plant extracts of varying concentrations were mixed with 2850 μL FRAP solution (25 mL acetate buffer (300 mM, pH 3.6), 2.5 mL 2-4-6 tripyridyl-s-triazine (10 mM in 40 mM hydrochloric) (TPTZ; Sigma-Aldrich, Sydney, Australia), and 2.5 mL hydrated ferric chloride solution (20 mM) previously equilibrated for 30 minutes in the dark at 37°C). The reaction was allowed to take place for 30 minutes in the dark. The absorbance was determined at 593 nm. All determinations were done in triplicate and data obtained were expressed as mM Trolox Equivalent (TE)/mg crude extract.

2.10. Nitric Oxide Radical Scavenging Assay

Nitric oxide (NO) was generated from sodium nitroprusside (SNP) (Sigma-Aldrich, Sydney, Australia) and was measured by the Griess Ilosvay reagent [25], using 0.1% w/v naphthylethylene-diamine-dihydrochloride (Sigma-Aldrich, Sydney, Australia) instead of 5% 1-naphthylamine. Plant extract (0.5 mL) was added to a mixture containing SNP (2 mL) and phosphate buffer saline (PBS) (0.5 mL, pH 7.4). The reaction mixture was incubated for 2.5 hrs at 25°C. Following incubation, 0.5 mL of the reaction mixture was added to 1 mL sulphanilic acid (0.33% in 20% glacial acetic acid) (Sigma-Aldrich, Sydney, Australia) and allowed to stand for 5 minutes. Naphthylethylene-diamine-dihydrochloride (1 mL of 0.1% w/v) was then added to the mixture. The resulting solution was vortexed and allowed to stand for further 30 minutes. The absorbance of the chromophores formed during the diazotization of nitrite with sulphanilamide and subsequent coupling with naphthylethylene-diamine-dichloride was read at 546 nm. Percentage inhibition was calculated as follows:

2.11. DPPH Free Radical Scavenging Assay

The free radical scavenging activity of the different extracts was measured by using 1,1-diphenyl-2-picrylhydrazyl (DPPH) (Sigma-Aldrich, Sydney, Australia) according to the modified method of Umamaheswari and Chatterjee [26]. Plant extract (100 μL) was added to 200 μL freshly prepared DPPH solution (100 μM in methanol). The reaction mixture was incubated at 37°C for 30 minutes. After incubation, absorbance was determined at 517 nm. The percentage inhibition of DPPH was calculated using (4).

2.12. Xanthine Oxidase Inhibitory Activity

The xanthine oxidase (Sigma-Aldrich, Germany) inhibitory activity was determined using modified method of Abdullahi et al. [27]. Samples were assayed for their in vitro xanthine oxidase inhibitory activity which was evaluated spectrophotometrically using xanthine as the substrate. The assay mixture consisted of 1 mL of the fraction, 2.9 mL phosphate buffer (pH 7.5), and 2 mL xanthine (0.15 mM) prepared in buffer. The mixture was vortexed and left to stand for 15 minutes. After 15 minutes, 0.1 mL of xanthine oxidase enzyme solution (0.1 unit/mL in phosphate buffer, pH 7.5), prepared immediately before use, was added. The mixture was then incubated at ambient temperature for 30 minutes. After the incubation period, reaction was stopped by the addition of 1 mL of 1 M hydrochloric acid. The absorbance was measured at 290 nm using a UV spectrometer. Allopurinol (100 μL/mL), a known inhibitor of XO, was used as a positive control. One unit of XO is defined as the amount of enzyme required to produce 1 mmol of uric acid/min at 25°C. XO inhibitory activity was expressed as the percentage inhibition of XO by using the following equation:where represents the activity of the enzyme without plant extract and is the activity of XO in the presence of plant extract.

2.13. Determination of Total Phenol, Flavonoid, and Anthocyanin Tannin Content

The total phenolic content was evaluated using the modified Folin-Ciocalteu assay described by Nickavar and Esbati [28]. The plant extract (0.50 mL) was added to a test-tube containing a tenfold diluted Folin-Ciocalteu reagent solution (2.50 mL) and sodium carbonate (2.00 mL, 7.5%). The mixture was allowed to react for 30 minutes at room temperature. The total phenolic content was then spectrophotometrically determined at 760 nm. All determinations were carried out in triplicate and results obtained were expressed as μg gallic acid equivalent (GAE)/mg crude extract.

The total flavonoid content was evaluated according to the aluminium chloride colorimetric method [29]. The plant extract (2 mL) was added to 2% aluminium chloride solution (2 mL). The mixture was allowed to react for 30 minutes at room temperature and the absorbance was read at 420 nm. All determinations were performed in triplicate and results obtained were expressed as μg rutin equivalent (RE)/mg crude extract.

The total anthocyanin content was calculated using the pH differential method [30]. Briefly, 1 mL of plant extract was transferred into 10 mL volumetric flask and the volume was adjusted with buffer pH 1.0 and pH 4.5. Mixtures were allowed to equilibrate for 15 minutes. Absorbance of each dilution was spectrophotometrically determined at 510 and 700 nm. Absorbance of diluted samples was evaluated using the following equation:

The monomeric anthocyanin pigment concentration in the original sample was calculated according to the following equation:where MW is the molecular weight of cyanidin-3-glucoside (484.5), DF the dilution factor, and the molar extinction coefficient (26,900).

Quantitative estimation of tannin, as catechin equivalent, was evaluated using the vanillin-HCl method with slight modifications. Extract (1 mL) was added in 5 mL of reagent mix containing 4% vanillin (in methanol) and 8% concentrated hydrochloric acid (in methanol). The resulting reaction mixture was vortexed and kept in the dark for 20 minutes. The absorbance was then determined at 500 nm using a spectrophotometer, using catechin (400 μg/mL) as standard.

2.14. Statistical Analysis

All data were expressed as means ± SD for 3 experiments. Statistical analyses were performed using statistical software, namely, SPSS version 21.0 for Windows 7 and Excel software (Microsoft 2010).

3. Results

3.1. Inhibitory Activity of Aloe vera Gel on Key Enzymes

Data obtained from the α-amylase inhibition assay (Table 1) indicated no enzyme inhibitory activity for the Aloe vera extract when compared to the positive control (Acarbose, 400 μg/mL) which had percentage of inhibition (%). Results from α-glucosidase inhibition assay showed no enzyme inhibitory activity for the Aloe vera extract when compared to the positive control (Acarbose, 5 mg/mL). Aloe vera gel exhibits a significantly higher () percentage inhibition of % than the positive control (Orlistat, 0.48 mM) against pancreatic lipase.

SamplePercentage inhibition
α-amylaseα-glucosidasePancreatic lipase

Acarbose96.64 ± 0.1062.70 ± 0.1570.58 ± 0.50
Aloe vera−4.88 ± 0.09−0.81 ± 0.3385.56 ± 0.91

compared to the control (Acarbose), one-way ANOVA.
3.2. Enzyme Kinetic Studies

Aloe vera was further assessed through kinetic studies to determine the type of inhibition on pancreatic lipase (Figure 2). The Lineweaver-Burk plot was generated using the calibration curve of nitrophenol, mentioned in Section 2. The double reciprocal Lineweaver-Burk plots showed a decrease in maximal velocity () and an increase in Michaelis-Menten constant (), thereby suggesting mixed inhibition. decreases from () mM min−1 to () mM min−1 while increases from 0.99 to 10.66.

3.3. Effect of Aloe vera Gel on Glucose Movement In Vitro

Figure 3 shows that Aloe vera mimics the action of Arabic gum (positive control) and thus retards glucose movement considerably. No significant difference () was observed between the positive control and Aloe vera gel. The glucose content in dialysate and GDRI are depicted in Tables 2 and 3, respectively.

SampleGlucose content in dialysate (mg/mL)One-way ANOVA ()
1 hour2 hours3 hours4 hours value

Arabic gum
Aloe vera
0.057 ± 0.005
0.057 ± 0.005
0.136 ± 0.003
0.124 ± 0.003
0.171 ± 0.003
0.165 ± 0.005
0.185 ± 0.001
0.185 ± 0.005

SampleGlucose diffusion retardation index
1 hour2 hours3 hours4 hours

Arabic gum 99549914 99439949
Aloe vera 99549923 99459949

3.4. Antimicrobial Screening

Aloe vera gel did not inhibit the growth of any of the microbes tested (Table 4). However, when compared to the blank, the results showed a less intensive red colour for Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. This tends to suggest that Aloe vera (though it did not inhibit bacterial growth) showed reduced growth. The controls used against bacteria are Streptomycin, Chloramphenicol, and Ciprofloxacin while the one used against fungi is Amphotericin.

Antimicrobial strainsMIC (mg/mL)
Aloe veraStreptomycinChloramphenicolCiprofloxacinAmphotericin

Staphylococcus aureus0.0020.004No growth
Escherichia coli0.0160.002No growth
Pseudomonas aeruginosa0.0080.063No growth
Candida albicans0.063
Candida tropicalis0.063

3.5. Antioxidant Activities of Aloe vera Gel

In FRAP assay, the antioxidant activity was determined by generating the standard curve in the range of 0–400 μM and the results were expressed as mM Trolox Equivalent (TE)/mg crude extract (, ). Aloe vera gel showed a value of  mM Trolox Equivalent (TE). Table 5 shows the percentage inhibition of Aloe vera in the different assays. Aloe vera gel exhibits significantly lower percentage inhibition against DPPH and free radicals than the corresponding control (). It also inhibits xanthine oxidase at a significantly lower percentage than the control ().

AssaysPercentage inhibitionOne-way ANOVA
Aloe veraControl value

DPPH free radical scavenging assay17.11 ± 1.3081.78 ± 0.247153.206<0.05
NO scavenging assay34.88 ± 0.5287.25 ± 0.749935.925<0.05
Xanthine oxidase inhibitory assay73.85 ± 2.0285.94 ± 0.11106.801<0.05

Ascorbic acid (400 μg/mL), ascorbic acid (2 mg/mL), and allopurinol (100 μg/mL).
3.6. Phytochemical Screening

Total phenolic content is reported as gallic acid equivalents by reference to standard curve ( and ) and was found to be  mg GAE/g of extract. The total flavonoid content was μg rutin equivalent (RE)/mL crude extract, respectively, by reference to standard curve ( and ). Aloe vera also showed a total tannin content of μg catechin equivalent by reference to standard curve ( and ). No anthocyanin was found. The results are summarised in Table 6.

AssaysAloe vera

Total phenolic content66.06 ± 1.14
Total flavonoid content60.95 ± 0.97
Total tannin content21.11 ± 1.92
Total anthocyanin contentND

μg gallic acid equivalent (GAE)/mg, μg rutin equivalent (RE)/mg, and μg catechin equivalent; ND: not detected.

4. Discussion

In the present study, unprocessed Aloe vera gel was assessed in terms of its ability to inhibit key carbohydrate hydrolysing enzymes. No significant inhibition was found explaining that the antidiabetic property of Aloe vera gel may not be due to enzyme inhibition. This contradicts the findings of Abu Soud et al., where dried Aloe vera crude extract showed significant (more than 80%) α-amylase inhibitory activity [3133]. These disparities can be explained based on the fact that different extraction method was used. Another study reported moderate α-amylase inhibitory activity with low percentage inhibition by Aloe vera extracts [33]. However, the previous study has used soxhlet apparatus where dried plant parts were finely crushed, powdered, and extracted with methanol [34]. Methanol and ethanol are more efficient than water in cell walls and seeds degradation which have nonpolar character and cause active ingredients to be released from cells [35]. The decrease in activity of aqueous extract can also be ascribed to the enzyme polyphenol oxidase, which degrades polyphenols in water extracts but is inactive in methanol and ethanol [35]. Additionally, ethanol was found to penetrate the cellular membrane more easily to extract the intracellular ingredients from the plant material [35].

Dialysis tubing technique is a simple model to evaluate the potential of soluble dietary fibres to retard the diffusion and movement of glucose in the intestinal tract [36, 37]. There are experimental evidences suggesting that the retardation of the nutrient flow into the external medium is an indication of the modulating effect of fibre on glucose absorption in the intestine [36]. Hence, this assay may help to evaluate the hypoglycaemic effect of a particular extract. The effects of plant extracts on glucose movement in vitro have gained much attention due to the fact that in recent years national and international diabetes associations have emphasised the need to increase fibre intake which interacts with food nutrients reducing absorption, especially postprandial glucose after carbohydrate-rich meals [38].

In the present study, Aloe vera gel proved to be an efficient agent to retard glucose movement across the dialysis tubing. It followed almost the same trend as Arabic gum, used as a control. As reported by Ahmed et al., the retardation in glucose diffusion might be attributed to the physical obstruction towards glucose molecules or the entrapment of glucose molecules within the fibre network [39]. Hence, it can be deduced that the viscous and mucilaginous nature of Aloe vera gel entrapped the glucose molecules preventing them from moving into the external solution. The results thus support the use of Aloe vera gel to maintain blood glucose level in diabetic patients. The diabetic activity could also be attributed to reduced intestinal absorption of postprandial glucose, in order to prevent high peaks of glucose in the blood. Most of the studies carried out on the antidiabetic properties of Aloe vera used homogenised or processed Aloe vera extract. To our best knowledge, no information concerning effect of Aloe vera gel (in its natural form) on antidiabetic activities has been published. Abo-Youssef and Messiha [13] reported the antidiabetic role of Aloe vera and explained that this could be due to the potent antioxidant potential of Aloe vera. Another study used aqueous extract of Aloe vera (100 g Aloe vera boiled with 200 mL distilled water and then cooled) which was fed to diabetic rats which in turn resulted in lowered blood glucose level [40].

A varying range of lipases, responsible for the catalysis of hydrolysis of ester bonds in triacylglycerols, are produced by the human body [41]. Some pharmacological obesity treatments, for example, Orlistat, function through specific, irreversible inhibition of gastrointestinal lipases, of which pancreatic lipase is the most biologically active and important one in healthy humans [41]. Serious adverse effects are commonly reported for Orlistat, including steatorrhoea, bloating, oily spotting, faecal urgency, and faecal incontinence that can affect up to 40% of patients [41]. Hence, a product which inhibits pancreatic lipase and lowers/eliminates the adverse effects of present treatment would be of substantial benefit to patients.

The present study attempted to probe into the hypolipidemic effect of Aloe vera gel through the inhibition of pancreatic lipase. The results showed that Aloe vera gel exhibited a significantly higher percentage of inhibition than the positive control Orlistat. Furthermore, kinetics parameters were evaluated from the double reciprocal plot for Aloe vera gel. The results showed an increase in the Michaelis constant () and a decrease in maximal velocity () of the reaction, suggesting a mixed inhibition of pancreatic lipase. This is a major type of inhibition that occurs when the inhibitor is capable of binding to both the free-enzyme and the enzyme-substrate complex. Generally, when the inhibitor binds favourably to the free-enzyme, mixed inhibition leads to an increase in value while if it binds preferentially to the enzyme-substrate complex, value is decreased. Both cases are accompanied by a decrease in . In the present study, an increase in and a decrease in were observed suggesting that Aloe vera gel has a greater affinity for the free-enzyme that is pancreatic lipase. This offers the advantage of not being affected by higher concentrations of substrate compared to Orlistat which acts as a competitive inhibitor [42]. Our result tends to support a study conducted by Kim et al. [43] which showed that the administration of processed Aloe vera gel lowered triacylglyceride levels in liver. Additionally, the plasma and histological examinations of periepididymal fat pad showed that processed Aloe vera gel reduced the average size of adipocytes. Choi et al. [12] showed reduced body weight, body fat mass, and insulin resistance in obese individuals treated with Aloe vera. Choudhary et al. also proved the efficacy of Aloe vera by showing significant reduction in blood glucose, lipid profile, and blood pressure of the diabetic patients [44]. According to the present study’s results, it can be deduced that Aloe vera gel inhibits porcine pancreatic lipase and thus deserves to be further explored as a weight lowering agent to combat obesity.

The present study also aimed to investigate the antimicrobial attributes of Aloe vera gel. The extract was tested against 5 common microorganisms. Results clearly demonstrate that Aloe vera gel, in its natural form, does not inhibit microbial growth. This tends to contradict results obtained by Khaing, where he demonstrated that Aloe vera inhibited numerous human pathogens except Candida albicans [45]. The present results also contradicted the results obtained by Nejatzadeh-Barandozi [46], where Aloe vera suppressed the growth of Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa amongst others. The disparity can be explained by the use of ethanol extract which contains more bioactive components than the unprocessed Aloe vera gel. Hence, it can be deduced from preliminary data gathered in the present study that unprocessed Aloe vera gel is not an effective antimicrobial agent.

Reactive oxygen species (ROS) have potent oxidative effects on cellular constituents which can in turn impair cellular functions [47]. Therefore, they are associated with pathogenesis of insulin resistance via the inhibition of insulin signals and dysregulation of adipocytokines/adipokines which play an important role in the progression of diabetes, hypertension, atherosclerosis, and even cancer [48]. Scavenging of free radicals is believed to be a valuable measure to prevent or treat diseases like diabetes mellitus [49].

For the determination of antioxidant properties of Aloe vera gel, different antioxidant assays like DPPH, NO, FRAP, and xanthine oxidase inhibitory assay were performed. Aloe vera gel showed low DPPH and scavenging abilities in the current study. Though significantly lower than the positive control, it is evident that the extract did show some proton-donating ability and could serve as free radical inhibitor or scavenger, acting possibly as antioxidants. The results however contradict the findings of Khaing [45]. The latter proved that Aloe vera had strong DPPH scavenging ability. The difference can be explained by the fact that 95% ethanol Aloe vera extract was used which has a higher percentage yield of bioactive ingredients. Yet, here also, the antioxidant activity was not as high as the positive controls. Another study compared the antioxidant activity of Aloe vera extracted in different solvents and obtained highest DPPH inhibition in methanol extract of Aloe vera [34]. The results also displayed xanthine oxidase inhibition. Xanthine oxidase is a form of xanthine oxidoreductase, a type of enzyme that generates ROS. These enzymes catalyze the oxidation of hypoxanthine to xanthine and can further convert the oxidation of xanthine to uric acid. Aloe vera gel also showed significant ferric reducing antioxidant power which adds up to its antioxidant properties. However, a study showed that Aloe vera extracts obtained from supercritical carbon dioxide extraction and ethanol showed stronger antioxidant activities than BHT and α-tocopherol [50].

Over the past 10 years, there has been a growing interest in the potential of polyphenols among researchers and food manufacturers mainly because of their antioxidant properties, their abundance in our diet, and their role in the prevention of various diseases associated with oxidative stress such as cancer, cardiovascular disease, and neurodegeneration [46]. Polyphenols are reputed for their antioxidant activities and these compounds are multifunctional and can act as reducing agents, hydrogen-donating antioxidants, and singlet oxygen quenchers. The current study showed that Aloe vera gel possesses significant amount of phenols and flavonoids which contribute to the antioxidant activities but contain little tannins and no anthocyanins. This support the findings of Patel et al. [51] which reported that the Aloe vera extract contained significant amount of phenol, flavonoids, berberine, and gallic acid through HPLC techniques. However, the crude Aloe vera extract used in the experiments was from a commercial source.

Therefore, the present in vitro study has provided sound scientific footing to enhance assurance on the traditional remedy of Aloe vera, which may be efficient as a preventive agent in the pathogenesis of some diseases. It is anticipated that data amassed in the present study will open new avenues for the development of potential drugs that can be used to treat and/or manage DM, obesity, and related complications.

Conflict of Interests

The authors declare that they have no competing interests.

Authors’ Contribution

M. Fawzi Mahomoodally and Urmeela Taukoorah designed the study and contributed to the preparation of the paper. Both authors read and approved the final paper.


  1. F. Mahomoodally, “Let food be thy medicine: exotic fruits and vegetables as therapeutic components for obesity and other metabolic syndromes,” in Novel Plant Bioresources: Applications in Food, Medicine and Cosmetics, A. Gurib-Fakim, Ed., pp. 350–351, Wiley-Blackwell, 1st edition, 2014. View at: Google Scholar
  2. B. O. Akinyele and A. C. Odiyi, “Comparative study of vegetative morphology and the existing taxonomic status of Aloe vera L.,” Journal of Plant Sciences, vol. 2, no. 5, pp. 558–563, 2007. View at: Publisher Site | Google Scholar
  3. V. K. Gupta and S. Malhotra, “Pharmacological attribute of Aloe vera: revalidation through experimental and clinical studies,” Ayu, vol. 33, no. 2, pp. 193–196, 2012. View at: Publisher Site | Google Scholar
  4. D. Vijayalakshmi, R. Dhandapani, S. Jayaveni, P. S. Jithendra, C. Rose, and A. B. Mandal, “In vitro anti inflammatory activity of Aloe vera by down regulation of MMP-9 in peripheral blood mononuclear cells,” Journal of Ethnopharmacology, vol. 141, no. 1, pp. 542–546, 2012. View at: Publisher Site | Google Scholar
  5. A. Ray, S. D. Gupta, and S. Ghosh, “Evaluation of anti-oxidative activity and UV absorption potential of the extracts of Aloe vera L. gel from different growth periods of plants,” Industrial Crops and Products, vol. 49, pp. 712–719, 2013. View at: Publisher Site | Google Scholar
  6. E. R. Rodríguez, J. D. Martín, and C. D. Romero, “Aloe vera as a functional ingredient in foods,” Critical Reviews in Food Science and Nutrition, vol. 50, no. 4, pp. 305–326, 2010. View at: Publisher Site | Google Scholar
  7. S. K. Gediya, R. B. Mistry, U. K. Patel, M. Blessy, and H. N. Jain, “Herbal plants: used as a cosmetics,” Journal of Natural Products and Plant Resources, vol. 1, no. 1, pp. 24–32, 2011. View at: Google Scholar
  8. M. N. Shahzad and N. Ahmed, “Effectiveness of Aloe vera gel compared with 1% silver sulphadiazine cream as burn wound dressing in second degree burns,” Journal of the Pakistan Medical Association, vol. 63, no. 2, pp. 225–230, 2013. View at: Google Scholar
  9. A. Oryan, A. Mohammadalipour, A. Moshiri, and M. R. Tabandeh, “Topical application of Aloe vera accelerated wound healing, modeling, and remodeling: an experimental study with significant clinical value,” Annals of Plastic Surgery, 2014. View at: Publisher Site | Google Scholar
  10. M. M. Budai, A. Varga, S. Milesz, J. Tozsér, and S. Benko, “Aloe vera downregulates LPS-induced inflammatory cytokine production and expression of NLRP3 inflammasome in human macrophages,” Molecular Immunology, vol. 56, no. 4, pp. 471–479, 2013. View at: Publisher Site | Google Scholar
  11. Z. Yu, C. Jin, M. Xin, and H. JianMin, “Effect of Aloe vera polysaccharides on immunity and antioxidant activities in oral ulcer animal models,” Carbohydrate Polymers, vol. 75, no. 2, pp. 307–311, 2009. View at: Publisher Site | Google Scholar
  12. H.-C. Choi, S.-J. Kim, K.-Y. Son, B.-J. Oh, and B.-L. Cho, “Metabolic effects of aloe vera gel complex in obese prediabetes and early non-treated diabetic patients: Randomized controlled trial,” Nutrition, vol. 29, no. 9, pp. 1110–1114, 2013. View at: Publisher Site | Google Scholar
  13. A. M. H. Abo-Youssef and B. A. Messiha, “Beneficial effects of Aloe vera in treatment of diabetes: comparative in vivo and in vitro studies,” Bulletin of Faculty of Pharmacy, Cairo University, vol. 51, no. 1, pp. 7–11, 2013. View at: Publisher Site | Google Scholar
  14. H. A. El-Shemy, M. A. M. Aboul-Soud, A. A. Nassr-Allah, K. M. Aboul-Enein, A. Kabash, and A. Yagi, “Antitumor properties and modulation of antioxidant enzymes' activity by Aloe vera leaf active principles isolated via supercritical carbon dioxide extraction,” Current Medicinal Chemistry, vol. 17, no. 2, pp. 129–138, 2010. View at: Publisher Site | Google Scholar
  15. Republic of Mauritius, National Diabetes Management System to be Introduced Shortly, Says Health Minister, 2015,,-says-Health-Minister-.aspx.
  16. M. I. Issack, V. N. Pursem, T. M. S. Barkham, L.-C. Ng, M. Inoue, and S. S. Manraj, “Reemergence of dengue in mauritius,” Emerging Infectious Diseases, vol. 16, no. 4, p. 716, 2010. View at: Publisher Site | Google Scholar
  17. W. W. Mao and J. E. Kinsella, “Amylase activity in banana fruit: properties and changes in activity with ripening,” Journal of Food Science, vol. 46, no. 5, pp. 1400–1403, 1981. View at: Publisher Site | Google Scholar
  18. G. Pistia-Brueggeman and R. I. Hollingsworth, “A preparation and screening strategy for glycosidase inhibitors,” Tetrahedron, vol. 57, no. 42, pp. 8773–8778, 2001. View at: Publisher Site | Google Scholar
  19. C.-D. Zheng, Y.-Q. Duan, J.-M. Gao, and Z.-G. Ruan, “Screening for Anti-lipase Properties of 37 Traditional Chinese Medicinal Herbs,” Journal of the Chinese Medical Association, vol. 73, no. 6, pp. 319–324, 2010. View at: Publisher Site | Google Scholar
  20. Y. Bustanji, A. Issa, M. Mohammad et al., “Inhibition of hormone sensitive lipase and pancreatic lipase by Rosmarinus officinalis extract and selected phenolic constituents,” Journal of Medicinal Plants Research, vol. 4, no. 21, pp. 2235–2242, 2010. View at: Google Scholar
  21. A. M. Gallagher, P. R. Flatt, G. Duffy, and Y. H. A. Abdel-Wahab, “The effects of traditional antidiabetic plants on in vitro glucose diffusion,” Nutrition Research, vol. 23, no. 3, pp. 413–424, 2003. View at: Publisher Site | Google Scholar
  22. C. A. Edwards, N. A. Blackburn, L. Craigen et al., “Viscosity of food gums determined in vitro related to their hypoglycemic actions,” The American Journal of Clinical Nutrition, vol. 46, no. 1, pp. 72–77, 1987. View at: Google Scholar
  23. A. J. Drummond and R. D. Waigh, “The development of microbiological methods for phytochemical screening,” Recent Research Developments in Phytochemistry, vol. 4, pp. 143–152, 2000. View at: Google Scholar
  24. I. F. F. Benzie and J. J. Strain, “The ferric reducing ability of plasma (FRAP) as a measure of ‘antioxidant power’: the FRAP assay,” Analytical Biochemistry, vol. 239, no. 1, pp. 70–76, 1996. View at: Publisher Site | Google Scholar
  25. P. Mandal, T. K. Misra, and M. Ghosal, “Free-radical scavenging activity and phytochemical analysis in the leaf and stem of Drymaria diandra Blume,” International Journal of Integrative Biology, vol. 7, no. 2, pp. 80–84, 2009. View at: Google Scholar
  26. M. Umamaheswari and T. Chatterjee, “In vitro antioxidant activities of the fractions of Coccinia grandis L. leaf extract,” African Journal of Traditional, Complementary and Alternative Medicines, vol. 5, no. 1, pp. 61–73, 2008. View at: Publisher Site | Google Scholar
  27. A. Abdullahi, R. Hamzah, A. Jigam et al., “Inhibitory activity of xanthine oxidase by fractions Crateva adansonii,” Journal of Acute Disease, vol. 1, no. 2, pp. 126–129, 2012. View at: Publisher Site | Google Scholar
  28. B. Nickavar and N. Esbati, “Evaluation of the antioxidant capacity and phenolic content of three Thymus species,” Journal of Acupuncture and Meridian Studies, vol. 5, no. 3, pp. 119–125, 2012. View at: Publisher Site | Google Scholar
  29. O. U. Amaeze, G. A. Ayoola, M. O. Sofidiya, A. A. Adepoju-Bello, A. O. Adegoke, and H. A. B. Coker, “Evaluation of antioxidant activity of Tetracarpidium conophorum (Müll. Arg) Hutch & Dalziel leaves,” Oxidative Medicine and Cellular Longevity, vol. 2011, Article ID 976701, 7 pages, 2011. View at: Publisher Site | Google Scholar
  30. J. Sutharut and J. Sudarat, “Total anthocyanin content and antioxidant activity of germinated colored rice,” International Food Research Journal, vol. 19, no. 1, pp. 215–221, 2012. View at: Google Scholar
  31. P. Kumar, M. Mehta, S. Satija, and M. Garg, “Enzymatic in vitro anti-diabetic activity of few traditional Indian medicinal plants,” Journal of Biological Sciences, vol. 13, no. 6, pp. 540–544, 2013. View at: Publisher Site | Google Scholar
  32. S. Pulipaka, S. R. Challa, and R. B. Pingili, “Comparative antidiabetic activity of methanolic extract of Operculina turpethum stem and root against healthy and streptozotocin induced diabetic rats,” International Current Pharmaceutical Journal, vol. 1, no. 9, pp. 272–278, 2012. View at: Publisher Site | Google Scholar
  33. R. S. Abu Soud, I. I. Hamdan, and F. U. Afifi, “Alpha amylase inhibitory activity of some plant extracts with hypoglycemic activity,” Scientia Pharmaceutica, vol. 72, no. 1, pp. 25–33, 2004. View at: Google Scholar
  34. V. Saritha, K. R. Anilakumar, and F. Khanum, “Antioxidant and antibacterial activity of Aloe vera gel extracts,” International Journal of Pharmaceutical and Biological Archive, vol. 1, no. 4, pp. 376–384, 2010. View at: Google Scholar
  35. P. Tiwari, B. Kumar, M. Kaur, G. Kaur, and H. Kaur, “Phytochemical screening and extraction: a review,” Internationale Pharmaceutica Sciencia, vol. 1, no. 1, pp. 98–106, 2011. View at: Google Scholar
  36. D. Qujeq and A. Babazadeh, “The entrapment ability of aqueous and ethanolic extract of Teucrium polium: glucose diffusion into the external solution,” International Journal of Molecular and Cellular Medicine, vol. 2, no. 2, pp. 93–96, 2013. View at: Google Scholar
  37. C. M. Picot, A. H. Subratty, and F. M. Mahomoodally, “Inhibitory potential of five traditionally used native antidiabetic medicinal plants on alpha-amylase, alpha-glucosidase, glucose entrapment and amylolysis kinetics in-vitro,” Advances in Pharmacological Sciences, vol. 2014, Article ID 739834, 7 pages, 2014. View at: Publisher Site | Google Scholar
  38. M. O. Weickert and A. F. H. Pfeiffer, “Metabolic effects of dietary fiber consumption and prevention of diabetes,” Journal of Nutrition, vol. 138, no. 3, pp. 439–462, 2008. View at: Google Scholar
  39. F. Ahmed, N. S. Siddaraju, and A. Urooj, “In vitro hypoglycemic effects of Gymnema sylvestre, Tinospora cordifolia, Eugenia jambolana and Aegle marmelos,” Journal of Natural Pharmaceuticals, vol. 2, no. 2, pp. 52–55, 2011. View at: Publisher Site | Google Scholar
  40. S. A. J. Saif-Ur-Rehman, S. Hassan, I. Ahmed, and M. Naim, “Study on Antidiabetic effect of Aloe vera extract on alloxan induced diabetic rats,” Libyan Agriculture Research Center Journal Internation, vol. 2, no. 1, pp. 29–32, 2011. View at: Google Scholar
  41. B. S. Drew, A. F. Dixon, and J. B. Dixon, “Obesity management: update on orlistat,” Vascular Health and Risk Management, vol. 3, no. 6, pp. 817–821, 2007. View at: Google Scholar
  42. V. Ghadyale, S. Takalikar, V. Haldavnekar, and A. Arvindekar, “Effective control of postprandial glucose level through inhibition of intestinal alpha glucosidase by Cymbopogon martinii (Roxb.),” Evidence-Based Complementary and Alternative Medicine, vol. 2012, Article ID 372909, 6 pages, 2012. View at: Publisher Site | Google Scholar
  43. K. Kim, H. Kim, J. Kwon et al., “Hypoglycemic and hypolipidemic effects of processed Aloe vera gel in a mouse model of non-insulin-dependent diabetes mellitus,” Phytomedicine, vol. 16, no. 9, pp. 856–863, 2009. View at: Publisher Site | Google Scholar
  44. M. Choudhary, A. Kochhar, and J. Sangha, “Hypoglycemic and hypolipidemic effect of Aloe vera L. in non-insulin dependent diabetics,” Journal of Food Science and Technology, vol. 51, no. 1, pp. 90–96, 2014. View at: Publisher Site | Google Scholar
  45. T. A. Khaing, “Evaluation of the antifungal and antioxidant activities of the leaf extract of Aloe vera (Aloe barbadensis Miller),” World Academy of Science, Engineering and Technology, vol. 75, pp. 610–612, 2011. View at: Google Scholar
  46. F. Nejatzadeh-Barandozi, “Antibacterial activities and antioxidant capacity of Aloe vera,” Organic and Medicinal Chemistry Letters, vol. 3, no. 1, p. 5, 2013. View at: Publisher Site | Google Scholar
  47. M. Carocho and I. C. F. R. Ferreira, “A review on antioxidants, prooxidants and related controversy: natural and synthetic compounds, screening and analysis methodologies and future perspectives,” Food and Chemical Toxicology, vol. 51, no. 1, pp. 15–25, 2013. View at: Publisher Site | Google Scholar
  48. M. Matsuda and I. Shimomura, “Increased oxidative stress in obesity: implications for metabolic syndrome, diabetes, hypertension, dyslipidemia, atherosclerosis, and cancer,” Obesity Research and Clinical Practice, vol. 7, no. 5, pp. e330–e341, 2013. View at: Publisher Site | Google Scholar
  49. L. Fu, B.-T. Xu, R.-Y. Gan et al., “Total phenolic contents and antioxidant capacities of herbal and tea infusions,” International Journal of Molecular Sciences, vol. 12, no. 4, pp. 2112–2124, 2011. View at: Publisher Site | Google Scholar
  50. Q. Hu, Y. Hu, and J. Xu, “Free radical-scavenging activity of Aloe vera (Aloe barbadensis Miller) extracts by supercritical carbon dioxide extraction,” Food Chemistry, vol. 91, no. 1, pp. 85–90, 2005. View at: Publisher Site | Google Scholar
  51. D. K. Patel, K. Patel, B. Duraiswamy, and S. P. Dhanabal, “Phytochemical analysis and standardization of Strychnos nux-vomica extract through HPTLC techniques,” Asian Pacific Journal of Tropical Disease, vol. 2, no. 1, pp. S56–S60, 2012. View at: Publisher Site | Google Scholar

Copyright © 2016 Urmeela Taukoorah and M. Fawzi Mahomoodally. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.