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Article

Effects of Citrus aurantium (Bitter Orange) Fruit Extracts and p-Synephrine on Metabolic Fluxes in the Rat Liver

by
Jéssica Sereno Peixoto
,
Jurandir Fernando Comar
,
Caroline Tessaro Moreira
,
Andréia Assunção Soares
,
Andrea Luiza De Oliveira
,
Adelar Bracht
* and
Rosane Marina Peralta
Department of Biochemistry, University of Maringá, Avenida Colombo 5790, 87020900 Maringá, Brazil
*
Author to whom correspondence should be addressed.
Molecules 2012, 17(5), 5854-5869; https://doi.org/10.3390/molecules17055854
Received: 21 March 2012 / Revised: 7 May 2012 / Accepted: 12 May 2012 / Published: 16 May 2012
(This article belongs to the Collection Bioactive Compounds)
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Abstract

:
The fruit extracts of Citrus aurantium (bitter orange) are traditionally used as weight-loss products and as appetite supressants. An important fruit component is p-synephrine, which is structurally similar to the adrenergic agents. Weight-loss and adrenergic actions are always related to metabolic changes and this work was designed to investigate a possible action of the C. aurantium extract on liver metabolism. The isolated perfused rat liver was used to measure catabolic and anabolic pathways, including oxygen uptake and perfusion pressure. The C. aurantium extract and p-synephrine increased glycogenolysis, glycolysis, oxygen uptake and perfusion pressure. These changes were partly sensitive to α- and β-adrenergic antagonists. p-Synephrine (200 μM) produced an increase in glucose output that was only 15% smaller than the increment caused by the extract containing 196 μM p-synephrine. At low concentrations the C. aurantium extract tended to increase gluconeogenesis, but at high concentrations it was inhibitory, opposite to what happened with p-synephrine. The action of the C. aurantium extract on liver metabolism is similar to the well known actions of adrenergic agents and can be partly attributed to its content in p-synephrine. Many of these actions are catabolic and compatible with the weight-loss effects usually attributed to C. aurantium.

Graphical Abstract

1. Introduction

Citrus aurantium (Rutaceae) is popularly known as “bitter orange” and its fruit extracts are being marketed and traditionally used as herbal weight-loss products and as appetite suppressants, although in Traditional Chinese Medicine they are prescribed in concert with other support herbs [1,2,3,4]. More recently bitter orange extracts have been demonstrated to possess anxiolytic and sedative properties [5]. The alkaloids p-synephrine and to a lesser extent octopamine (Figure 1) are believed to be the most active components of C. aurantium. However, the peels of the fruits also contain terpenes, furocumarines and flavonoids, including hesperidin, neohesperidin, naringin and tangaretin [6,7]. The p-synephrine content of the dried fruit extracts has been reported to be between 3% to 6% [8,9,10,11]. The alkaloids of C. aurantium are structurally related to the adrenergic amines ephedrine (Ephedra sinica), epinephrine, norepinephrine and m-synephrine (Figure 1). The latter is a vasoactive isomer of p-synephrine whose presence in C. aurantium has been suggested, but not confirmed [12,13]. Like the other adrenergic amines, p-synephrine is believed to act via α- and β-adrenoreceptors [2,14,15]. Lower binding affinities of these receptors for p-synephrine, however, have been reported when compared to norepinephrine and m-synephrine, for example. There are well fundamented suggestions, however, that binding of p-synephrine to β3 adrenoreceptors, which are associated to thermogenesis and lipolysis, could be a significant factor of the physiological action of the compound [15]. C. aurantium extracts marketed for weight-loss are prepared from dried fruit peels and may be associated with other compounds, mainly caffeine [16]. Despite its inclusion in over-the-counter weight-loss products, little evidence supports the use of C. aurantium alone to treat overweight and obesity [11]. It has been shown that extracts increase lipolysis, thermogenesis and weight loss in both animal models and humans, but always tested in combination with other compounds, especially caffeine, which is also known to enhance the thermogenic properties of herbal weight-loss preparations [2,11]. As the C. aurantium extracts, p-synephrine effectively promoted weight loss or thermogenesis in human models only in combination with other stimulants [17,18,19], although in pure form it was effective in mice and rats [4,8,20].
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Figure 1. Structural formulae of the C. aurantium alkaloids synephrine, octopamine and related amines.
Figure 1. Structural formulae of the C. aurantium alkaloids synephrine, octopamine and related amines.
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Weight loss is always associated to metabolic effects. The liver is the metabolic organ par excellence and one can expect that p-synephrine, as an adrenergic agonist, should affect liver metabolism. It is known, for example, that epinephrine, norepinephrine and other adrenergic agonists stimulate glycogenolysis and gluconeogenesis in the liver via α- and β-adrenoreceptors [21,22,23,24,25,26,27,28]. Up to now there are no studies about the action of C. aurantium and p-synephrine on liver metabolism and the present work reports our first attempts at addressing this matter. More specifically, we have used the isolated perfused rat liver to investigate the actions of C. aurantium extracts and p-synephrine on glycogenolysis, glycolysis and gluconeogenesis. Additionally we have also measured portal perfusion pressure and oxygen uptake, the latter being a parameter that in the liver is largely dependent on the oxidation of fatty acids. An important goal of our study was to find out if the effects of a commercial C. aurantium extract, the most usual formulation that is consumed for therapeutic purposes, can be explained basically for its p-synephrine contents.

2. Results and Discussion

2.1. Effects of C. aurantium on Glycogen Catabolism, Glycolysis, Oxygen Uptake

The first experiments were planned in order to test the possible effects of C. aurantium on glycogen catabolism and glycolysis. When perfused with substrate-free medium the livers from fed rats survive at the expense of the oxidation of endogenous fatty acids (major route) and glycolysis from endogenous glycogen (minor route). Under these conditions the livers release glucose, lactate and pyruvate as a result of glycogen catabolism [29]. Figure 2 illustrates the responses of perfused livers to the infusion of a C. aurantium extract at the concentration of 400 mg/L. It also illustrates a typical experimental protocol, which was used for all other extract concentrations. After a pre-perfusion period of 10 min, the C. aurantium extract was infused during 20 min. This was followed by additional 10 min of extract-free perfusion. Four parameters were measured: glucose release, lactate and pyruvate production and oxygen consumption. As noted in Figure 2, all parameters were stable before the initiation of C. aurantium infusion. After the onset of the infusion, however, oxygen uptake increased and remained so during the entire infusion period. Glucose release and lactate production were also increased with peak values 200 and 100% above the basal values, respectively. Pyruvate production was not changed. After removing the extract from the perfusion fluid, the stimulations of glucose release and lactate production returned to their basal levels. The recovery of oxygen consumption, however, was incomplete.
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Figure 2. Time courses of the changes caused by the C. aurantium extract (400 mg/L) on glycogen catabolism and endogenous fatty acids-driven oxygen uptake. Livers from fed rats were perfused as described in the Experimental Section. C. aurantium (400 mg/L) was infused during 20 min, as indicated by the horizontal bar. The effluent perfusate was sampled in 2-min intervals and analyzed for glucose, lactate, and pyruvate. Oxygen consumption was followed polarographically. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
Figure 2. Time courses of the changes caused by the C. aurantium extract (400 mg/L) on glycogen catabolism and endogenous fatty acids-driven oxygen uptake. Livers from fed rats were perfused as described in the Experimental Section. C. aurantium (400 mg/L) was infused during 20 min, as indicated by the horizontal bar. The effluent perfusate was sampled in 2-min intervals and analyzed for glucose, lactate, and pyruvate. Oxygen consumption was followed polarographically. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
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Experiments like those illustrated in the Figure 2 were repeated with 25, 50, and 100 mg/L of C. aurantium extract in order to investigate the concentration dependence of the effects. The mean results are shown in Figure 3A and represent the final values of each parameter at the end of the drug infusion period (25–30 min perfusion time in Figure 2). Oxygen consumption, glycogenolysis (glucose plus ½[pyruvate + lactate]) and glycolysis (pyruvate plus lactate) were represented against the C. aurantium extract concentration. As revealed by Figure 3A, the C. aurantium extract increased almost linearly both glycogenolysis and glycolysis in the range up to 400 mg/L (196 μM synephrine). Oxygen uptake, however, was already maximal at the concentration of 25 mg/L (12.3 μM synephrine) with no significant modifications in the range up to 400 mg/L.Figure 3B shows the changes caused by the C. aurantium extract on the lactate to pyruvate ratio, which is an indicator of the cytosolic NADH/NAD+ ratio [30]. It is apparent that the extract produced a considerable increase in the lactate to pyruvate ratio (200% at the concentration of 400 mg/L). It is noteworthy to mention that all these effects of the C. aurantium extract, stimulations of glycogenolysis, glycolysis and oxygen uptake, were also reported for the adrenergic agonists epinephrine [23,24], norepinephrine [25,26] and phenylephrine [26]. These effects are different from those of glucagon which, while stimulating glycogenolysis and oxygen uptake, strongly inhibits glycolysis [23].
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Figure 3. Concentration dependences of the effects of the C. aurantium extract on glycogen catabolism and endogenous fatty acids-driven oxygen uptake. Data were obtained from experiments of the kind illustrated by Figure 2. Glycogenolysis and glycolysis are expressed as glucosyl units and were calculated as glucose production +½(lactate production + pyruvate production) and lactate production + pyruvate production, respectively. Each datum point represents the mean of three liver perfusion experiments. Bars are standard errors of the mean. Asterisks and crosses indicate statistical significance in comparison with the control condition as revealed by variance analysis with post hoc Student-Newman-Keuls testing (+ p< 0.05, ** p < 0.01).
Figure 3. Concentration dependences of the effects of the C. aurantium extract on glycogen catabolism and endogenous fatty acids-driven oxygen uptake. Data were obtained from experiments of the kind illustrated by Figure 2. Glycogenolysis and glycolysis are expressed as glucosyl units and were calculated as glucose production +½(lactate production + pyruvate production) and lactate production + pyruvate production, respectively. Each datum point represents the mean of three liver perfusion experiments. Bars are standard errors of the mean. Asterisks and crosses indicate statistical significance in comparison with the control condition as revealed by variance analysis with post hoc Student-Newman-Keuls testing (+ p< 0.05, ** p < 0.01).
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To verify if oxygen uptake stimulation comes from the mitochondria, the microsomal electron transport chain or from both, experiments were done with cyanide, which at the concentration of 2 mM completely blocks the mitochondrial respiratory chain [29]. The results are shown in Figure 4. As expected cyanide greatly inhibited oxygen uptake. The infusion of the C. aurantium extract in the presence of cyanide showed only a discrete increase in oxygen uptake. This is strongly indicative for a predominantly mitochondrial origin of the C. aurantium effects on oxygen consumption.
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Figure 4. Effects of the C. aurantium extract on oxygen uptake in the presence of cyanide. Livers from fed rats were perfused as described in the Experimental Section. The infusion of cyanide was started after stabilization of oxygen uptake. The times at which infusion of cyanide and C. aurantium extracts (400 mg/L) were started are indicated. Oxygen consumption was followed polarographically. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
Figure 4. Effects of the C. aurantium extract on oxygen uptake in the presence of cyanide. Livers from fed rats were perfused as described in the Experimental Section. The infusion of cyanide was started after stabilization of oxygen uptake. The times at which infusion of cyanide and C. aurantium extracts (400 mg/L) were started are indicated. Oxygen consumption was followed polarographically. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
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Stimulation of oxygen uptake in the liver from fed rats perfused with substrate-free medium represents mainly an increased oxidation of endogenous fatty acids [29]. The source includes already existent free fatty acids as well as fatty acids arising from lipolysis [31]. The latter is stimulated by adrenergic agents, as indeed demonstrated for p-synephrine in isolated lipocytes [32]. This is a typically catabolic process, but it is not necessarily thermogenic in nature. In fact, it has been shown that stimulation of oxygen uptake by the adrenergic agonist epinephrine is accompanied by a significant increase in the mitochondrial ATP content without significant changes in the cytosolic content [23]. This overall increase in the cellular ATP content is, in principle, not indicative of a merely thermogenic activity of adrenergic agents in the liver.

2.2. Effects of C. aurantium on Gluconeogenesis and Oxygen Consumption Due to Lactate Infusion in Livers from Fasted Rats

The experiments shown in Figure 5 were planned to investigate a possible action of C. aurantium on gluconeogenesis from lactate. In order to minimize interference by glycogen catabolism, livers from 18 h fasted rats were used. Figure 5 illustrates the responses of the perfused livers to the C. aurantium extract infusion at the concentration of 400 mg/L. After a pre-perfusion period of 10 min with substrate-free medium, 2 mM lactate was infused during 30 min, followed by additional 20 min of C. aurantium extract plus lactate infusion. The infusion of 2 mM lactate produced a rapid and sustained increase in glucose and pyruvate production and also in oxygen uptake. The infusion of 400 mg/L C. aurantium produced non-significant oscillations in oxygen uptake and inhibitions of pyruvate and glucose production. The latter was more strongly inhibited than the former.
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Figure 5. Time courses of the effects of the C. aurantium extract on gluconeogenesis from lactate and related parameters in perfused livers from fasted rats. Livers from fasted rats were perfused as described in the Experimental Section. Lactate (2 mM) and Citrus aurantium were infused as indicated by the horizontal bars. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
Figure 5. Time courses of the effects of the C. aurantium extract on gluconeogenesis from lactate and related parameters in perfused livers from fasted rats. Livers from fasted rats were perfused as described in the Experimental Section. Lactate (2 mM) and Citrus aurantium were infused as indicated by the horizontal bars. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
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The effects on lactate metabolism caused by the C. aurantium extract at the concentration of 400 mg/L might not be the same at lower concentrations. For this reason the experiments illustrated by Figure 5 were repeated with extract concentrations in the range between 25 and 200 mg/L. The results are summarized in Figure 6 which shows the final values of the variables measured at the end of the C. aurantium extract infusion period (50–60 min perfusion time) as a function of the concentration. Figure 6 shows that the C. aurantium extract clearly increased oxygen uptake in the concentration range between 25 and 200 mg/L. Inhibition occurred only at the concentration of 400 mg/L. This was also the only concentration that produced a clear inhibition of glucose production. At the lowest extract concentrations (especially 25 mg/L) a stimulatory tendency was apparent, but statistical significance was lacking. Pyruvate production, finally, was clearly inhibited at low extract concentrations, maximal inhibition occurring at the concentration of 50 mg/L.
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Figure 6. Effects of the C. aurantium extract on gluconeogenesis and related parameters: concentration dependences. The experimental protocol was the same illustrated by Figure 5. Each datum point is the mean of three experiments. Asterisks and crosses indicate statistical significance in comparison with the control condition as revealed by variance analysis with post hoc Student-Newman-Keuls testing (+ p < 0.05, ** p < 0.01).
Figure 6. Effects of the C. aurantium extract on gluconeogenesis and related parameters: concentration dependences. The experimental protocol was the same illustrated by Figure 5. Each datum point is the mean of three experiments. Asterisks and crosses indicate statistical significance in comparison with the control condition as revealed by variance analysis with post hoc Student-Newman-Keuls testing (+ p < 0.05, ** p < 0.01).
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2.3. Effects of p-Synephrine on Glycogen Catabolism, Oxygen Uptake and Gluconeogenesis

Since p-synephrine is the main active component of C. aurantium, experiments were designed to investigate the effect of p-synephrine. The experimental protocols of these experiments were similar to those used in the experiments with the C. aurantium extracts. The p-synephrine concentration was 200 μM, which is practically the same molar concentration of this component that can be expected when the extract is infused at a concentration of 400 mg/L (196 μM). Figure 7 shows the results of the experiments in which glycogen catabolism and oxygen uptake in livers from fed rats were measured. Comparison of Figure 2 and Figure 7 reveals immediately that the effects of 400 mg/L extract and of 200 μM p-synephrine were very similar in qualitative terms. Quantitatively, however, some differences were observed. p-Synephrine (200 μM) produced an increase in glucose output of 1.73 μmol·min−1·g−1, an effect that was only 15% smaller than the increment caused by the extract (400 mg/L) containing 196 μM p-synephrine, which was equal to 2 μmol·min−1·g−1. For oxygen consumption stimulation, however, the difference was much more pronounced, 0.28 μmol·min−1·g−1 for p-synephrine and 0.45 μmol·min−1·g−1 for the extract (60% difference). It seems, thus, that p-synephrine is not the only agent in the C. aurantium extract capable of changing metabolic parameters in the liver.
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Figure 7. Time courses of the effects of 200 µM p-synephrine on glycogen catabolism and fatty acid-driven oxygen uptake. Livers from fed rats were perfused as described in the Experimental Section. p-Synephrine (200 µM) was infused during 20 min, as indicated. The effluent perfusate was sampled in 2-min intervals and analyzed for glucose, lactate and pyruvate. Oxygen consumption was followed polarographically. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
Figure 7. Time courses of the effects of 200 µM p-synephrine on glycogen catabolism and fatty acid-driven oxygen uptake. Livers from fed rats were perfused as described in the Experimental Section. p-Synephrine (200 µM) was infused during 20 min, as indicated. The effluent perfusate was sampled in 2-min intervals and analyzed for glucose, lactate and pyruvate. Oxygen consumption was followed polarographically. Each datum point represents the means of three liver perfusion experiments. Bars are standard errors of the mean.
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The effects of 200 μM p-synephrine on lactate gluconeogenesis were also investigated. The results are shown in Figure 8 . In this case comparison of Figure 5 and Figure 8 reveals different actions of the extract containing 196 μM p-synephrine and 200 μM pure p-synephrine, except for pyruvate production which was inhibited. p-Synephrine did not inhibit gluconeogenesis, actually a clear stimulatory tendency which persisted during the whole infusion period was apparent. Oxygen uptake was also stimulated during the whole perfusion period of p-synephrine. These results strongly corroborate the hypothesis raised above that not all effects of the extract are caused by p-synephrine. However, it should be recalled that the lactate stimulated respiration was not inhibited by the extract at low concentrations (Figure 6).
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Figure 8. Effects of p-synephrine on lactate gluconeogenesis and related parameters in perfused livers from fasted rats. Livers from fasted rats were perfused as described in the Experimental Section. Lactate (2 mM) and p-synephrine were infused as indicated by the horizontal bars.
Figure 8. Effects of p-synephrine on lactate gluconeogenesis and related parameters in perfused livers from fasted rats. Livers from fasted rats were perfused as described in the Experimental Section. Lactate (2 mM) and p-synephrine were infused as indicated by the horizontal bars.
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Actually stimulation was found. Furthermore, inhibition of gluconeogenesis, which is not an adrenergic effect, occurred only at the highest extract concentration (400 mg/L). This suggests that the additional and non-adrenergic effects of the extract only manifest themselves at high concentrations. They could well be non-significant under in vivo conditions.

2.4. Influence of Adrenergic Antagonists on the Actions of the C. aurantium Extract

In order to obtain a first insight about the involvement of adrenergic signaling in the actions of the C. aurantium extract experiments were done in which the influence of four adrenergic antagonists was quantified. The antagonists were prazosin (α1 antagonist; [22]), yohimbine (α1 and α2 antagonist; [22]) propranolol (β1 and β2 antagonist; [21]) and SR59230A (a β3 antagonist; [33]). The results are shown in Table 1. In this series of experiments the portal perfusion pressure was also measured taking into account the fact that adrenergic agonists are generally vasoactive [22,27]. The experimental protocol was similar to that one illustrated by Figure 2, with a pre-perfusion period for evaluating the basal rates and portal perfusion pressure and a subsequent infusion of the C. aurantium extract (400 mg/mL) during 20 min. For testing the action of the adrenergic antagonists these substances were infused alone during 10 min prior to initiating the C. aurantium extract infusion (400 mg/mL). The infusion of the antagonists was continued during the C. aurantium extract infusion. The parameters that were monitored were evaluated in terms of the differences between the values found in the simultaneous presence of the C. aurantium extract and the antagonist and the values found before the extract infusion. None of the antagonists had any effect on the metabolic parameters or perfusion pressure in the absence of the C. aurantium extract (not shown). However, most of them had some influence on the effects of the C. aurantium extract. The notable exception was SR59230A, which had no significant effects on both metabolic parameters and hemodynamics. The basal portal perfusion pressure was equal to 3.63 ± 0.13 mm Hg. The modification caused by the C. aurantium extract shown in Table 1 represents, thus, a 2.6-fold increase.
Table
Table 1. Effects of various antagonists on the effects of the Citrus aurantium extract on glycogen catabolism, oxygen uptake and perfusion pressure. Livers from fed rats were perfused with Krebs/Henseleit-bicarbonate. For the control experiments, the experimental protocol illustrated by Figure 2 was used. In the experiments in which the antagonists were infused, the Citrus aurantium extract infusion was preceded by the infusion of one of the three antagonists (10 min). The concentrations were: Citrus aurantium extract, 400 mg/mL;prazosin, 10 μM; yohimbine, 100 μM; propranolol, 50 μM; and SR59230A, 10 μM. Glucose and lactate production and oxygen uptake were measured as described in the Experimental Section. The portal perfusion pressure was monitored by means of a pressure transducer. Values represent the mean increments (± mean standard errors; n = 3–4) produced by the Citrus aurantium extract under the various conditions. Asterisks indicate statistical signficance at the 5% level when compared to the control condition (Citrus aurantium extract alone) as revealed by variance analysis with post-hoc testing (Student-Newman-Keuls).
Table 1. Effects of various antagonists on the effects of the Citrus aurantium extract on glycogen catabolism, oxygen uptake and perfusion pressure. Livers from fed rats were perfused with Krebs/Henseleit-bicarbonate. For the control experiments, the experimental protocol illustrated by Figure 2 was used. In the experiments in which the antagonists were infused, the Citrus aurantium extract infusion was preceded by the infusion of one of the three antagonists (10 min). The concentrations were: Citrus aurantium extract, 400 mg/mL;prazosin, 10 μM; yohimbine, 100 μM; propranolol, 50 μM; and SR59230A, 10 μM. Glucose and lactate production and oxygen uptake were measured as described in the Experimental Section. The portal perfusion pressure was monitored by means of a pressure transducer. Values represent the mean increments (± mean standard errors; n = 3–4) produced by the Citrus aurantium extract under the various conditions. Asterisks indicate statistical signficance at the 5% level when compared to the control condition (Citrus aurantium extract alone) as revealed by variance analysis with post-hoc testing (Student-Newman-Keuls).
Perfusate conditionsΔ Portal pressure (mm Hg)Δ Oxygen uptake (μmol min−1 g−1)Δ Glucose release (μmol min−1 g−1)Δ Lactate production (μmol min−1 g−1)
Citrus aurantium extract alone (control)5.81 ± 1.000.54 ± 0.081.86 ± 0.120.80 ± 0.08
Citrus aurantium extract + prazosin0.92 ± 0.01 *0.44 ± 0.090.32 ± 0.03 *0.26 ± 0.09 *
Citrus aurantium extract + yohimbine0.10 ± 0.04 *0.22 ± 0.03 *0.04 ± 0.01 *0.38 ± 0.04 *
Citrus aurantium extract + propranolol2.60 ± 0.75 *0.31 ± 0.010.34 ± 0.03 *0.55 ± 0.14
Citrus aurantium extract + SR59230A5.99 ± 0.850.53 ± 0.031.88 ± 0.140.60 ± 0.17
Yohimbine almost abolished this increase and prazosin had also a strong inhibitory effect. The action of propranolol was much less pronounced. Stimulation of glucose release (glycogenolysis) was also almost abolished by yohimbine, and strongly inhibited by both prazosin and propranolol. Oxygen uptake stimulation was much less sensitive to the antagonists and the action of prazosin and propranolol even lacked statistical significance. Lactate production (glycolysis) was more strongly affected by prazosin. The actions of the adrenergic antagonists in Table 1 present a relatively complex picture but they certainly indicate that both α- and β-adrenergic receptors are involved in the actions of the C. aurantium extract. It can even be said that the participation of β-adrenergic receptors is less important in the case of the portal pressure increase and the stimulation of lactate production. The exact contribution of α- or β-receptors, however, cannot be inferred from the present data. This is a question that requires exhaustive experimental work in which the actions of individual compounds found in C. aurantium (e.g., p-synephrine and octopamine) must be examined for their sensitivity to specific antagonists of the various classes of adrenergic receptors. Cross-talking between various signaling pathways is also a highly probable event which deserves attention. The lack of effects of SR59230A indicates, in principle at least, that the hepatic effects observed in the present work are not elicited by binding of p-synephrine to β3-adrenergic receptors although there is evidence that these receptors are present in the liver [34,35]. It should be stressed, however, that it seems well documented that p-synephrine acts via these receptors in other tissues [15].

3. Experimental

3.1. Materials and Animals

The liver perfusion apparatus was built in the workshops of the University of Maringá. p-Synephrine, enzymes and coenzymes used in the enzymatic assays were purchased from Sigma-Aldrich Co (St. Louis, MO, USA). Commercial C. aurantium dried extracts were purchased from the company Pharma Nostra (Rio de Janeiro, Brazil; lot ZS071226). The extracts were manufactured by the Shanxi Company (China, lot 08041136D-2008). The manufacturer indicates that the concentration of p-synephrine in the extracts is higher than 6% and chemical analysis by Pharma Nostra indicated 8.2% synephrine. All other chemicals were from the best available grade (98–99.8% purity) and were purchased from Sigma-Aldrich, Merck (Darmstadt, Germany) and Reagen ( Rio de Janeiro, Brazil).
Male Wistar rats weighing 200–280 g were used in all experiments. Animals were fed ad libitum with a standard laboratory diet (Nuvilab®, Colombo, Brazil) and maintained on a regulated light-dark cycle. In accordance with the requirements of the experimental protocols, fed rats as well as 18 h fasted rats were used. For the surgical procedure, the rats were anesthetized by intraperitoneal injection of sodium pentobarbital (50 mg/Kg). The criterion of anesthesia was the lack of body or limb movement in response to a standardized tail clamping stimulus. All experiments were done in accordance with the world-wide accepted ethical guidelines for animal experimentation.

3.2. Liver Perfusion

Hemoglobin-free, non-recirculating perfusion was performed [29,36]. After cannulation of the portal and cava veins the liver was positioned in a plexiglass chamber. The constant perfusate flow was provided by a peristaltic pump (Minipuls 3, Gilson, Villier Le Bel, France) and adjusted between 30 and 33 mL per min, depending on the liver weight. The perfusion fluid was Krebs/Henseleit-bicarbonate buffer (pH 7.40) containing 25 mg% bovine-serum albumin, saturated with a mixture of oxygen and carbon dioxide (95:5) by means of a membrane oxygenator with simultaneous temperature adjustment (37 °C). The composition of the Krebs/Henseleit-bicarbonate buffer is the following: 115 mM NaCl, 25 mM NaHCO3, 5.8 mM KCl, 1.2 mM Na2SO4, 1.18 mM MgCl2, 1.2 mM NaH2PO4 and 2.5 mM CaCl2. The perfusion fluid enters the liver via the portal vein cannula and leaves the organ through the cava vein cannula. Samples of the effluent perfusion fluid were collected and analyzed for their metabolite contents. C. aurantium and p-synephrine were added to the perfusion fluid at the desired concentrations (up to 200 mg/L).

3.3. Analytics

In the effluent perfusion fluid the following compounds were assayed by means of standard enzymatic procedures: glucose, lactate and pyruvate [37]. The oxygen concentration in the outflowing perfusate was monitorated continuously, employing a Teflon-shielded platinum electrode adequately positioned in a plexiglass chamber at the exit of the perfusate [29,36]. Metabolic rates were calculated from input-output differences and the total flow rates and were referred to the wet weight of the liver.
The portal perfusion pressure was monitored by means of a pressure transducer (Hugo Sachs Elektronic-Harvard Apparatus GmbH, March-Hugstetten, Germany). The sensor was positioned near the entry of the portal vein, and the transducer was connected to a recorder [38]. The pressure changes were computed from the recorder tracings and expressed as millimeters of mercury (mm Hg).

3.4. Statistical Analysis

The error parameters presented in the graphs are standard errors of the means. Statistical analysis was performed with the GraphPad Prism Software® (version 5.0; Graph Pad Software, San Diego, CA, USA). The Student’s t test was applied and the 5% level (p < 0.05) was adopted as a criterion of significance.

4. Conclusions

The results of the present work reveal that the metabolic action of the C. aurantium extract on liver metabolism and portal perfusion pressure is similar to the actions of other adrenergic agents. The same applies to p-synephrine, which is generally considered to be the main active component of C. aurantium. The sensitivity to adrenergic agonists is strong evidence that several effects are indeed mediated by adrenergic signaling pathways. Since many of the actions of C. aurantium are mainly catabolic in nature, e.g., increased glycolysis and oxygen uptake dependent on fatty acid oxidation, it can be concluded that they are, in principle at least, compatible with the weight-loss effects usually attributed to C. aurantium.

Acknowledgments

The authors wish to thank the financial support of the Conselho Nacional de Desenvolvimento Cientifico e Tecnológico (CNPq) and the Fundação Araucária.

References and Notes

  1. Preuss, H.G.; Diferdinando, D.; Bagchi, M.; Bagchi, D. Citrus aurantium as a thermogenic, weight-reduction replacement for ephedra: An overview. J. Med. 2002, 33, 246–264. [Google Scholar]
  2. Fugh-Berman, A.; Meyers, A. Citrus aurantium, an ingredient of dietary supplements marketed for weight loss: Current status of clinical and basic diseases. Exp. Biol. Med. 2004, 229, 698–704. [Google Scholar]
  3. Arias, B.A.; Ramón-Laca, L. Pharmacological properties of citrus and their ancient and medieval uses in the Mediterranean region. J. Ethnopharmacol. 2005, 97, 89–95. [Google Scholar] [CrossRef]
  4. Stohs, S.J.; Preuss, H.G.; Shara, M. The safety of Citrus aurantium (bitter orange) and its primary protoalkaloid p-synephrine. Phytother. Res. 2011, 25, 1421–1428. [Google Scholar] [CrossRef]
  5. Carvalho-Freitas, M.I.R.; Costa, M. Anxiolytic and sedative effects of extracts and essential oil from Citrus aurantium L. Biol. Pharm. Bull. 2002, 25, 1629–1633. [Google Scholar] [CrossRef]
  6. Pellati, F.; Benvenuti, S.; Melegari, M.; Firenzuoli, F. Determination of adrenergic agonists from extracts and herbal products of Citrus aurantium L. var. amara by LC. J. Pharm. Biomed. Anal. 2002, 29, 1113–1119. [Google Scholar] [CrossRef]
  7. Pellati, F.; Benvenuti, S.; Melegari, M. High-performance liquid chromatography methods for the analysis of adrenergic amines and flavanones in Citrus aurantium L. var. amara. Phytochem. Anal. 2004, 15, 220–225. [Google Scholar] [CrossRef]
  8. Arbo, M.D.; Schmitt, G.C.; Limberger, M.F.; Charão, M.F.; Moro, A.M.; Ribeiro, G.L.; Dallegrave, E.; Garcia, S.C.; Leal, M.B.; Limberger, R. Subchronic toxicity of Citrus aurantium L. (Rutaceae) extract and p-synephrine in mice. Regul. Toxicol. Pharmacol. 2009, 54, 114–117. [Google Scholar] [CrossRef]
  9. Avula, B.; Upparapalli, S.K.; Navarrete, A. Simultaneous quantification of adrenergic amines and flavonoids in C. aurantium, various Citrus species, and dietary supplements by liquid chromatography. J. AOAC Int. 2005, 88, 1593–1606. [Google Scholar]
  10. Andrade, A.S.; Schimitt, G.C.; Rossato, L.G.; Russowsky, D.; Limberger, R.P. Gas chromatographic method for analysis of p-synephrine in Citrus aurantium L. products. Chromatographia 2009, 69, S225–S229. [Google Scholar] [CrossRef]
  11. Haaz, S.; Fontaine, K.R.; Cutter, G.; Limdi, N.; Perumean-Chaney, S.; Allison, D.B. Citrus aurantium and synephrine alkaloids in the treatment of overweight and obesity: An update. Obes. Rev. 2006, 7, 79–88. [Google Scholar] [CrossRef]
  12. Allison, D.B.; Cutter, G.; Poehlman, E.T.; Moore, D.R.; Barnes, S. Exactly which synephrine alkaloids does Citrus aurantium (Bitter Orange) contain? Int. J. Obes. 2005, 20, 443–446. [Google Scholar]
  13. Greenway, F.; De Jonge-Levitan, L.; Martin, C.; Roberts, A.; Grundy, I.; Parker, C. Dietary herbal supplements with phenylephrine for weight loss. J. Med. Food 2006, 9, 572–578. [Google Scholar] [CrossRef]
  14. Brown, C.M.; Mcgrath, J.C.; Midgley, J.M.; Muir, A.G.; O’Brien, J.W.; Thonoor, C.M.; Williams, C.M.; Wilson, V.G. Activities of octopamine and synephrine stereoisomers on alpha-adrenoreceptors. Br. J. Pharmacol. 1988, 93, 417–429. [Google Scholar] [CrossRef]
  15. Stohs, S.J.; Preuss, H.G.; Shara, M. A review of the receptor-binding properties of p-synephrine as related to its pharmacological effects. Oxid. Med. Cell. Longev. [CrossRef]
  16. Blanck, H.M.; Serdula, M.K.; Gillespie, C.; Galuska, D.A.; Sharpe, P.A.; Conway, J.M.; Khan, L.K.; Ainsworth, B.E. Use of nonprescription dietary supplements for weight loss is common among americans. J. Am. Diet Assoc. 2007, 107, 441–447. [Google Scholar]
  17. Hoffman, J.R.; Kang, J.; Ratamess, N.A.; Rashti, S.L.; Tranchina, C.P.; Faigenbaum, A.D. Thermogenic effect of an acute ingestion of a weight loss supplement. J. Int. Soc. Sport. Nutr. 2009, 6, 1–6. [Google Scholar] [CrossRef]
  18. Carpéné, C.; Galitzky, J.; Fontana, E.; Atgié, C.; Lafontan, N.; Berlan, M. Selective activation of beta3-adrenoreceptors by octopamine: Comparative studies in mammalian fat cells. Naunyn Schmiedebergs Arch. Pharmacol. 1999, 359, 310–321. [Google Scholar] [CrossRef]
  19. Rossato, L.G.; Costa, V.M.; Limberger, R.P.; Bastos, M.L.; Remião, F. Synephrine: From trace concentration to massive consumption in weight-loss. Food Chem. Toxicol. 2011, 49, 8–16. [Google Scholar] [CrossRef]
  20. Calapai, G.; Firenzuoli, F.; Saitta, A.; Squadrito, F.; Arlotta, M.R.; Constantino, G.; Inferrera, G. Antiobesity and cardiovascular toxic effects of Citrus aurantium extracts in the rat: A preliminary report. Fitoterapia 1999, 70, 586–592. [Google Scholar] [CrossRef]
  21. Saitoh, Y.; Ui, M. Stimulation of glycogenolysis and gluconeogenesis by epinephrine independent of its beta-adrenergic function in perfused rat liver. Biochem. Pharmacol. 1976, 25, 841–845. [Google Scholar]
  22. Reinhart, P.H.; Taylor, W.M.; Bygrave, F.L. Studies on a-adrenergic-induced respiration and glycogenolysis in perfused rat liver. J. Biol. Chem. 1982, 257, 1906–1912. [Google Scholar]
  23. Soboll, S.; Scholz, R. Control of energy metabolism by glucagon and adrenaline in perfused rat liver. FEBS Lett. 1986, 205, 109–112. [Google Scholar] [CrossRef]
  24. Bazotte, R.B.; Constantin, J.; Curi, R.; Kemmelmeier, F.S.; Hell, N.S.; Bracht, A. The sensitivity of glycogenolysis to glucagon, epinephrine and cyanide in livers from rats in different metabolic conditions. Res. Commun. Chem. Pathol. Pharmacol. 1989, 64, 193–203. [Google Scholar]
  25. Yamamoto, N.S.; Ishii-Iwamoto, E.L.; Bracht, A. Activation of glycogenolysis by methotrexate. Influence of calcium and inhibitors of hormone action. Biochem. Pharmacol. 1992, 44, 781–787. [Google Scholar]
  26. Nascimento, E.A.; Yamamoto, N.S.; Bracht, A.; Ishii-Iwamoto, E.L. Naproxen inhibits hepatic glycogenolysis induced by Ca2+-dependent agents. Gen. Pharmacol. 1995, 26, 211–218. [Google Scholar] [CrossRef]
  27. Bracht, A.; Kouyoumdjian, M.; Ishii-Iwamoto, E.L.; Borges, D.R. Indicator injections and pressure monitoring as complementary tools for investigating microcirculatory changes in the liver. Trends Comp. Biochem. Physiol. 2002, 9, 1–16. [Google Scholar]
  28. Dufour, S.; Lebon, V.; Shulman, G.I.; Petersen, K.F. Regulation of net hepatic glycogenolysis and gluconeogenesis by epinephrine in humans. Am. J. Physiol. Endocrinol. Metab. 2009, 297, E231–E235. [Google Scholar] [CrossRef]
  29. Scholz, R.; Bücher, T. Hemoglobin-Free Perfusion of Rat Liver. In Control of Energy Metabolism, 1st; Chance, B., Estabrook, R.W., Williamson, J.R., Eds.; Academic Press: New York, NY, USA, 1965; pp. 393–414. [Google Scholar]
  30. Sies, H. Nicotinamide Nucleotide Compartmentation. In Metabolic Compartmentation, 1st; Sies, H., Ed.; Academic Press: London, UK, 1982; pp. 205–231. [Google Scholar]
  31. Menahan, L.A.; Wieland, O. The role of endogenous lipid in gluconeogenesis and ketogenesis of perfused rat liver. Eur. J. Biochem. 1969, 9, 182–188. [Google Scholar] [CrossRef]
  32. Mercarder, J.; Wanecq, E.; Chen, J.; Carpéné, C. Isopropylnorsynephrine is a stronger lipolytic agent in human adipocytes than synephrine and other amines present in Citrus aurantium. J. Physiol. Biochem. 2011, 67, 443–452. [Google Scholar] [CrossRef]
  33. Nisoli, E.; Tonello, C.; Landi, M.; Carruba, M.O. Functional studies of the first selective β3-adrenergic receptor antagonist SR 59230A in rat brown adipocytes. Mol. Pharmacol. 1996, 49, 7–14. [Google Scholar]
  34. Sanghani, M.P.; Scarpace, P.J. Atypical beta-adrenergic receptors in rat liver: Evidence for transient expression during aging. J. Gerontol. 1994, 49, B60–B64. [Google Scholar]
  35. Kasahara, H.; Muto, S.I.; Motokawa, Y.; Arisaka, N.; Kobayashi, S.; Souma, S.; Kuroda, J. β3-adrenoreceptor-mediated increased circulating transaminase levels in mice treated with its agonist BRL 37344. J. Toxicol. Sci. 2012, 35, 779–784. [Google Scholar]
  36. Bracht, A.; Ishii-Iwamoto, E.L.; Kelmer-Bracht, A.M. O estudo do metabolismo no fígado em perfusão. In Métodos de Laboratório em Bioquímica,, 1st; Bracht, A., Ishii-Iwamoto, E.L., Eds.; Editora Manole: São Paulo, Brazil, 2003; pp. 275–289. [Google Scholar]
  37. Bergmeyer, H.U. Methods of Enzymatic Analysis; Verlag Chemie-Academic Press: Weinheim, Germany, London, UK, 1974. [Google Scholar]
  38. Comar, J.F.; Suzuki-Kemmelmeier, F.; Bracht, A. The action of oxybutynin on haemodynamics and metabolism in the perfused rat liver. Basic Clin. Pharmacol. Toxicol. 2003, 93, 147–152. [Google Scholar]
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MDPI and ACS Style

Peixoto, J.S.; Comar, J.F.; Moreira, C.T.; Soares, A.A.; De Oliveira, A.L.; Bracht, A.; Peralta, R.M. Effects of Citrus aurantium (Bitter Orange) Fruit Extracts and p-Synephrine on Metabolic Fluxes in the Rat Liver. Molecules 2012, 17, 5854-5869. https://doi.org/10.3390/molecules17055854

AMA Style

Peixoto JS, Comar JF, Moreira CT, Soares AA, De Oliveira AL, Bracht A, Peralta RM. Effects of Citrus aurantium (Bitter Orange) Fruit Extracts and p-Synephrine on Metabolic Fluxes in the Rat Liver. Molecules. 2012; 17(5):5854-5869. https://doi.org/10.3390/molecules17055854

Chicago/Turabian Style

Peixoto, Jéssica Sereno, Jurandir Fernando Comar, Caroline Tessaro Moreira, Andréia Assunção Soares, Andrea Luiza De Oliveira, Adelar Bracht, and Rosane Marina Peralta. 2012. "Effects of Citrus aurantium (Bitter Orange) Fruit Extracts and p-Synephrine on Metabolic Fluxes in the Rat Liver" Molecules 17, no. 5: 5854-5869. https://doi.org/10.3390/molecules17055854

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