BioMed Research International

Volume 2013 (2013), Article ID 171059, 6 pages

http://dx.doi.org/10.1155/2013/171059

Research Article

Sympathomimetic Activity of a Hoodia gordonii Product: A Possible Mechanism of Cardiovascular Side Effects

Orsolya Roza,¹ Norbert Lovász,² István Zupkó,² Judit Hohmann,¹ and Dezső Csupor¹

¹Department of Pharmacognosy, University of Szeged, Eötvös u. 6, Szeged 6720, Hungary

²Department of Pharmacodynamics and Biopharmacy, University of Szeged, Eötvös u. 6, Szeged 6720, Hungary

Received 12 April 2013; Revised 30 August 2013; Accepted 2 October 2013

Academic Editor: Gail B. Mahady

Copyright © 2013 Orsolya Roza et al. 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.

Abstract.

Hoodia gordonii, a popular appetite suppressant, is widely used as an ingredient in many food supplements despite the fact that supporting scientific evidence is scarce. Recently alarming side effects of H. gordonii products (increased blood pressure and elevated pulse rate) have been reported. The aim of our study was to elucidate the underlying mechanism of these symptoms. A H. gordonii-containing product was tested for sympathomimetic activity. Isolated organ experiments on rat uterine rings revealed smooth muscle relaxant effect with a substantial component mediated through β-adrenergic receptors. Chromatographic comparison of the analyzed product and authentic plant material confirmed that the herbal product contained Hoodia spp. extract, and its cardiovascular effects may be linked to the compounds of the plant.

1. Introduction

According to WHO, 65% of the world’s population live in countries where overweight and obesity kills more people than underweight. Obesity has become an epidemic, while safe and effective pharmacotherapy is still absent [1]. Numerous medications have been introduced for the treatment of obesity, which primarily act on the adrenergic, dopaminergic, cannabinoid, and serotonergic systems [2]. Because of serious side effects, there is only one drug (orlistat) in the European Union, and two in the United States (orlistat and topiramate + phentermine) approved for long-term use in the treatment of obesity; consequently, there is a disparity between demand and supply [3]. As a result, a broad scale of natural weight-loss products are under exploration, and countless products are currently available in the market with insufficient supporting scientific evidence [4].

Hoodia gordonii (Masson) Sweet ex Decne. (Apocynaceae) is a succulent plant consumed by Bushmen in South Africa in order to reduce appetite [5]. Its proposed active compound for weight-loss P57, an oxypregnane glycoside, was shown to cause increased ATP production in the hypothalamus after intracerebroventricular administration [6]. However, this mechanism of action is debatable, as there was no detectable P57 in the brain after oral administration in CD1 female mice according to Madgula et al. [7]. Another possible explanation for its appetite suppressant properties is that P57 may also act on the bitter taste receptors resulting in the secretion of CCK [8].

Besides P57, numerous other pregnane glycosides, based on five aglycones, were identified as main constituents, of which 19 are glycosides of hoodigogenin A, a unique pregnane derivate that can be found only in Hoodia species [9–11]. Thirteen calogenin glycosides were also reported, as well as one compound with isoramanone aglycone [11, 12]. Furthermore, two constituents were isolated as the first two naturally occurring glycosides of 5(6→7) abeo-sterol aglycones, namely, hoodistanal and dehydrohoodistanal [11]. Further components belonging to the compound classes of sterols, fatty acids, and alcohols were detected in low concentrations using GC-FID and GC-MS methods [13]. Hoodia species are stapeliads, emitting fetid scents; thus, H. gordonii flower volatiles were studied, and 94 compounds were also reported [14].

Although controversial appetite-suppressant effects have been demonstrated in some in vivo experiments conducted on rats and chickens, human evidence is still lacking [6, 15–17]. The only available human clinical study reported no change in body weight or energy expenditure; however, administration of a purified H. gordonii extract was associated with significant increase in blood pressure and pulse rate [18]. Similar side effects have been reported to the Department of Pharmacognosy, University of Szeged, by consumers of a product available in the Hungarian market (Hoodia spray). Taking into consideration these alarming side effects and the popularity of H. gordonii among natural products used for weight management, the unknown mechanisms behind these side effects seemed to be worthy of detailed investigation.

Numerous effective weight loss drugs, like sibutramine or amphetamine derivatives were withdrawn from the market because of their serious side effects, including increased blood pressure and elevated pulse rate. Concerning that the chemical composition of Hoodia spp. is not yet fully mapped, it is also possible that a group of compounds other than pregnane glycosides may be responsible for the reported side effects or for the appetite suppressant activity of H. gordonii [9–12].

Our present work has focused on the effect of the above-mentioned Hoodia spray on β-adrenergic receptors in rat uterus to explore the potential role of β-adrenergic receptor agonist activity in the possible cardiovascular adverse effects of the plant. Adulteration among diet and weight management supplements occurs frequently by using active pharmaceuticals as adulterants to intensify the anticipated effect [19, 20]. Synthetic weight loss drugs also possess cardiovascular side effects; thus, we performed analytical comparison with authentic plant material and also tested the product for the presence of usually occurring adulterants. Mass spectrometry was applied to confirm the presence of P57, a marker compound of Hoodia species, and HPLC fingerprinting was also performed for comparison to confirm the authenticity of the product.

2. Materials and Methods

2.1. Materials

The aerial parts of Hoodia gordonii (Masson) Sweet ex Decne. were obtained from a local succulent plant nursery in Szeged, Hungary, and authenticated by one of the authors (Orsolya Roza). A voucher specimen (no. 812) has been preserved in the Herbarium of the Department of Pharmacognosy, University of Szeged, Szeged, Hungary. Fytofontana Dietceutical Hoodia spray (distributed by Herb-Pharma Hu Ltd., Budapest, Hungary), a medical device registered in Hungary, was bought in a local pharmacy in Szeged, Hungary. The composition of the product displayed on the package is the following: Hoodia gordonii extract (corresponding to 2.2 g plant material/2 mL solution), peppermint, and alcohol. Amphetamine and methamphetamine were obtained from Scientific Section, DSRRB/DOA/UNDCP (Vienna, Austria). Sibutramine was extracted previously in our lab [21]. Ephedrine was purchased from Phoenix Pharma Zrt (Budapest, Hungary).

2.2. Preparation of Extracts

Authentic Hoodia extract for HPLC and HPTLC comparison was prepared from 7 g fresh, ground plant material with 3 × 25 mL of AcNi, using ultrasonic bath (15 min). After filtration, the solution was evaporated to dryness under reduced pressure to yield 0.15 g of extract. The residue was dissolved in 2 mL of MeOH, filtered, and then evaluated by HPLC and HPTLC.

The Hoodia product contained alcohol, and since ethanol may alter β-adrenergic receptor binding affinity and smooth muscle contractility [22], 25 mL spray was evaporated to dryness, then the residue was dissolved to the original volume with physiological saline-dimethyl sulfoxide (95 : 5) and then filtered to perform organ baths studies.

2.3. High Pressure Liquid Chromatography

Chromatographic analyses of the authentic H. gordonii extract and the commercial product were performed on a Waters HPLC system (Waters Associates, Milford, MA, USA) with a Waters 600 controller and pump, equipped with a 2487 dual absorbance detector. The separation was carried out on a Kinetex XB-C18 (2.6 μm, 100 Å, 100 × 4.6 mm) column (Phenomenex, Torrance, USA), operated at 40°C. Injection volume of 20 μL was used. Chromatographic elution was accomplished by gradient solvent system consisting of MeOH, AcNi, and H₂O, according to the method published by Janssen et al. [23].

2.4. Thin Layer Chromatography

Thin layer chromatographic analyses were carried out on aluminium TLC sheets (20 × 20 cm), coated with silica gel 60 F₂₅₄ (Merck KgaA, Darmstadt, Germany). For each test, 10 μL of Hoodia spray and standard solutions were applied. For sibutramine a solvent system of toluene-MeOH 95 : 5 was used for development. After drying, visualization was obtained by spraying with Dragendorff reagent. For methamphetamine and amphetamine a mobile phase of MeOH-cc. NH₃ 100 : 1.5 was used. After spraying with Marquis reagent (cc. H₂SO₄-formalin 20 : 1.5) and heating at 110°C for 2 min, detection was performed under UV light (366 nm) [24]. Ephedrine identification was carried out according to the Ph. Eur. 5, using a solvent system of CH₂Cl₂-cc. NH₃-2-propanol 5 : 15 : 80 and ninhydrin reagent for spraying. The plate was heated at 110°C for 5 min for visualization.

2.5. HPTLC

HPTLC comparison of the product and the authentic Hoodia extract was carried out according to the method described by Rumalla et al., using silica gel coated 60 F₂₅₄ HPTLC plates (10 × 20 cm) (Merck KgaA, Darmstadt, Germany) [25]. CHCl₃-MeOH-H₂O 70 : 30 : 3 as mobile phase and anisaldehyde as visualization reagent were used. After drying, plates were heated at 110°C for 5 min.

2.6. Mass Spectrometry

Analyses were performed on an API 2000 triple quadrupole tandem mass spectrometer (AB Sciex Instruments, Foster, CA, USA). Data integration was performed with Analyst 1.5.2 software version (AB Sciex Instruments). Electrospray ionization interface was used with the source temperature of 250°C, operating in positive mode using multiple reaction monitoring (MRM). The following conditions were used: capillary voltage 5500; curtain gas pressure 10 psi; collusion gas pressure was 6 psi; nebulizer gas pressure 50 psi; auxiliary gas pressure 20 psi.

2.7. Animals

Animals were treated in accordance with the Directive of the Council of the European Communities (86/609/ECC) and the Hungarian Act XXVIII of 1998 on the Protection of Animals in Research (Section 32). Experiments involving animal subjects were carried out with the approval of the Hungarian Ethical Committee for Animal Research (registration number: IV./01758-2/2008). Sexually mature female Sprague-Dawley rats (body mass: 140–160 g, 50–60 days old) were mated in the early morning hours. Copulation was confirmed by the presence of a copulation plug or spermatozoa in the vagina. The day of copulation was considered to be the first day of pregnancy. The animals were housed in temperature- (20–23°C), humidity- (40–60%), and light- (12 h of light, 12 h of dark) regulated rooms, with water and standard rodent food (Bioplan Ltd., Isaszeg, Hungary) intake available ad libitum.

2.8. In Vitro Organ Bath Studies

Uteri were removed from nonpregnant rats in the estrus phase and from pregnant rats on day 22 of gestation. Five mm long muscle rings were sliced from the uterine horns and mounted vertically in an organ bath containing 10 mL of de Jongh solution (composition: 137 mM NaCl, 3 mM KCl, 1 mM CaCl₂, 1 mM MgCl₂, 12 mM NaHCO₃, 4 mM NaH₂PO₄, and 6 mM glucose, pH = 7.4). The organ bath was maintained at 37°C, and carbogen (95% O₂ + 5% CO₂) was bubbled through it. After mounting, the rings were equilibrated for 1 h before the experiments were undertaken, and the de Jongh solution was changed every 15 min. The initial tension of the preparation was set to about 1.5 g, which was relaxed to about 0.5 g at the end of equilibration. The tension of the myometrial rings was measured with a gauge transducer (SG-02; Experimetria Ltd., Budapest, Hungary) and recorded with SPEL Advanced ISOSYS Data Acquisition System (Experimetria Ltd., Budapest, Hungary) [26]. The uterus-relaxant effect of Hoodia spray was investigated on spontaneous and 25 mM KCl-induced contractions alone and in the presence of 10 μM propranolol. The extract was administered cumulatively (50 μL, 50 μL, 100 μL, 200 μL, and 400 μL) into the organ bath, and the effect of the solvent system was excluded in separate experiments. The tissue samples were incubated for 5 min with each concentration. Areas under the curves (AUCs) of 5-min periods were evaluated; the effect of the Hoodia preparation was expressed as percentages of the spontaneous and KCl-induced contractions preceding the administration of the tested substance. All experiments were carried out on at least 6 animals, and each reported value is given as the mean ± SEM. Unpaired t-test was used for statistical evaluation of the presence of propranolol. All calculations and statistical analyses were performed with Prism 5.0 computer software (Graph Pad Software Inc., San Diego, CA, USA).

3. Results and Discussion

3.1. HPLC and HPTLC Comparison of the Product and Extract

The HPLC chromatogram of the plant extract and the product showed similarity, having similar fingerprints between 16 and 36 min at 220 nm (Figure 1). Differences in peak heights and areas can be explained with the dissimilarity of extraction methods (in the product’s leaflet there was no referral to the extraction method applied). As other Hoodia species contain the same constituents, but in different ratios, the chance that Hoodia species other than H. gordonii being used in the preparation cannot be excluded [25]. In the chromatogram of the product, few other peaks occurred, possibly due to additives present in the spray, such as Mentha piperita. Regarding the colors and retention factors of the detected spots, HPTLC analysis (not shown) also confirmed the similarity of the product and the plant extract.

Figure 1: HPLC fingerprint chromatograms of Hoodia extract (blue) and Hoodia spray (black).

3.2. TLC Analyses for Adulterants

Amphetamine, methamphetamine, sibutramine, and ephedrine were not detected in the product.

3.3. Mass Spectrometric Authentication

The product was also tested for P57 by mass spectrometry in multiple reaction monitoring (MRM) mode. This method allows the reliable identification of molecules with known m/z values in complex mixtures, such as herbal extracts. In our experiments, P57, a characteristic compound of Hoodia, was chosen for mass spectrometric identification. LiCl₃ was added to the sample, to enhance sensitivity. Both m/z 311.3 and m/z 785.5 product ions were detected with the precursor ion m/z 885.5, indicating that P57 is present in the Hoodia spray. The aglycone was identified too, with the product ions of m/z 319.3 and m/z 337.3. All of these transitions have been reported in the literature for P57 [27].

3.4. In Vitro Organ Bath Studies

β-adrenergic agonists are reported to decrease food intake and exhibit anorectic properties [28]. Stimulation of β-adrenoceptors also results in different cardiovascular symptoms. Since cardiovascular side effects have been reported for H. gordonii extracts, the stimulation of β-adrenergic receptors seems to be a rational explanation for the mechanism of its anorectic action [18]. Both α- and β-adrenergic receptors play crucial roles in the motor activity of myometrial smooth muscle eliciting contraction and relaxation, respectively, rendering uterine preparations ideal for investigations of drugs with actions on the sympathetic system. In the presented set of in vitro organ bath experiments, the myometrial effects of the H. gordonii extract-containing product were monitored against spontaneous and KCl-stimulated contractions of uterine rings from nonpregnant and late-pregnant (day 22) rats. In order to separate the actions mediated through α- and β-adrenoceptors all experiments were performed with and without nonselective β-antagonist propranolol (10 μM). The product elicited a marked and concentration-dependent relaxation against both spontaneous and stimulated contractions. The inhibition of spontaneous contractility was significantly decreased in the presence of propranolol (Figure 2). The relaxation of KCl-stimulated uteri was not modified in the presence of propranolol. The relaxing effect of the spray was substantially less pronounced on uteri from late-pregnant animals, but propranolol significantly modified it. The gestation-dependent alteration in the myometrial action of substances acting on the sympathetic system could be explained by the changes in the receptor function during pregnancy. The nonpregnant uterus of the rat exhibits limited α-adrenoceptor-mediated contraction but efficiently relaxed by β-adrenergic stimulation. Late-pregnant myometrium is sensitive to both α- and β-adrenergic stimulation, and therefore, the overall response is determined by the receptor preference of the tested substance [26]. It is plausible that the limited relaxation of late-pregnant myometrium induced by the product is a consequence of a balanced α- and β-adrenoceptor stimulation which can be shifted towards increased contractility by blocking the action mediated through β-receptors.

(a)

(b)

(c)

(d)

Figure 2: Effects of Hoodia spray on spontaneous ((a) and (c)) and KCl-stimulated ((b) and (d)) contractility of uterine rings from nonpregnant ((a) and (b)) and late-pregnant ((c) and (d)) animals. Experiments were performed in the presence (■) and absence (□) of propranolol. *, **, and *** indicate , , and , respectively.

Based on the propranolol-sensitive component of the uterine action of the product, a sympathomimetic effect with substantial β-receptor-mediated contribution is proposed. Our results support the cardiovascular side effects reported in a human clinical trial.

As we have shown, Hoodia spray possesses sympathomimetic effects, which can manifest in both appetite suppression and increased thermogenesis, resulting in weight loss [29, 30]. Moreover, in the experiments performed in the US patent application, increased water consumption was recorded during feeding studies, which is a well-known effect of sympathomimetic agents, let alone the side effects, elucidated in the human clinical trial [17]. Chemical composition of Hoodia is not yet fully mapped. In the literature, primarily pregnane glycosides are in the focus; however, other potentially active constituents with sympathomimetic activity may also be present in the plant.

Sympathomimetic agents as amphetamine derivatives or sibutramine are effective in weight management, but due to their serious cardiovascular side effects, they were withdrawn from the market. In the case of H. gordonii, cardiovascular side effects and proposed anorectic property are reported, raising the questions whether these effects are caused by the same constituents; and if they are, whether the responsible compound is truly P57.

4. Conclusion

We have shown for the first time that a H. gordonii-containing product has sympathomimetic activity on rat uterus mediated through β-adrenergic receptors. HPLC and HPTLC tests were performed to compare the product with authentic plant material. Due to the frequent adulteration of food supplements, we also tested the Hoodia spray product for the presence of some frequently used adulterants having sympathomimetic property. Our experiments revealed that the analyzed product did contain Hoodia species extract and was void of known adulterants with sympathomimetic activity (amphetamine, methamphetamine, sibutramine, and ephedrine). Considering the large number of Hoodia-containing products in the market, the presented data should be regarded alarming, due to possible cardiovascular side effects of these supplements.

Acknowledgments

This work was supported by the New Hungary Development Plan Projects TÁMOP-4.2.2/B-10/1-2010-0012 and TÁMOP-4.2.2.A-11/1/KONV-2012-0035. This paper was realized in the frames of TÁMOP-4.2.4.A/2-11-1-2012-0001 “National Excellence Program—Elaborating and Operating an Inland Student and Researcher Personal Support System.” The project was subsidized by the European Union and cofinanced by the European Social Fund. The authors are grateful for Krisztián Csankó for his precious contribution to the analytical experiments.

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