Case Reports in Emergency Medicine
Volume 2015 (2015), Article ID 182951, 5 pages
http://dx.doi.org/10.1155/2015/182951

Case Report

Toxic Effects of Rhamnus alaternus: A Rare Case Report

H. Ben Ghezala,¹ N. Chaouali,² I. Gana,² S. Snouda,¹ A. Nouioui,² I. Belwaer,² J. Ouali,¹ M. Kaddour,¹ W. Masri,² D. Ben Salah,² D. Amira,² H. Ghorbal,² and A. Hedhili²

¹Teaching Department of Emergency and Intensive Care Medicine, Regional Hospital of Zaghouan, Street of Republic, 1100 Zaghouan, Tunisia
²Research Laboratory of Toxicology-Environment LR12SP07, Laboratory of Toxicology, Center for Emergency Medical Assistance, Montfleury, 1008 Tunis, Tunisia

Received 10 February 2015; Accepted 17 June 2015

Academic Editor: Aristomenis K. Exadaktylos

Copyright © 2015 H. Ben Ghezala 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.

In Tunisia, there are about 478 species of plants commonly used in folk medicine. Medicinal plants and herbal remedies used are responsible for 2% of intoxications listed by Tunisian National Poison Center. Most cases are related to confusion between edible plants and toxic plants lookalikes or to an excessive consumption of therapeutic plants. We report the case of a 58-year-old man admitted to the Emergency Department of the Regional Hospital of Zaghouan (Tunisia), with renal failure and rhabdomyolysis. The patient reported having daily consumption of a homemade tea based on Mediterranean Buckthorn roots, during the last 6 months to treat type 2 diabetes. The aim of this work was to establish an association between the consumption of the herbal remedy and the occurrence of both renal failure and rhabdomyolysis. No similar cases have been reported in recent literature.

1. Introduction

Herbal remedies have been used for centuries to treat a variety of diseases. Mediterranean Buckthorn (Rhamnus alaternus) has been used for therapeutic purposes and no toxicity effects have been documented. Rhamnus alaternus (Rhamnaceae) is a small tree located mainly in the north of Tunisia, where it is known as “Oud El-Khir.” It has traditionally been used as a diuretic, laxative, hypotensive drug and for the treatment of diabetes, hepatic, and dermatologic complications [1, 2]. Previous phytochemical studies have shown potent antioxidant, free radical scavenging, antimutagenic and antigenotoxic activities of flavonoids and phenol isolated from Rhamnus alaternus roots and leaves [3, 4].

2. Case Report

On February 1, 2013, a 58-year-old man was admitted to the Emergency Department of the Regional Hospital of Zaghouan (Tunisia), with dizziness, weakness, anorexia, and dyspnea. His blood pressure was 130/60 mmHg. The patient has a 15-pack-year history of smoking. He was a mason by occupation. He had 20-year back history of pulmonary tuberculosis and type 2 diabetes revealed one year ago. Two days before his admission, the patient experienced nausea, vomiting, anuria, and hematuria. He reported having daily consumption of a homemade drink based on Rhamnus alaternus roots, during the last 6 months, to control his blood glucose levels. On physical examination, the patient had myalgia. He had no other clinical signs.

Cytological reports and sputum smear were negative (three times) for pulmonary tuberculosis. Hepatitis B and hepatitis C serology were also negative. Chest X-ray was normal; blood and urine culture were negative. In renal ultrasonography, there was a significant difference in kidney sizes and the corticomedullary differentiation was altered. Laboratory tests showed glucose 14.44 mmol/L, creatinine 1190 μmol/L, blood urea nitrogen 66.77 mmol/L, creatine phosphokinase (CPK) 2129 UI/L, pH 7.10, a CRP of 8.7 mg/L, and a normal coagulation profile (Table 1). Three dialysis sessions were performed.

Table 1: Biochemical, hematologic, and blood gas parameters, before and after dialysis.

Blood tests
Before dialysis
After dialysis
Normal ranges
(adult male)

Day 4
Day 7
Day 9

Glucose
14.44
4.74
4.50
4.55
3.9–6.1 mmol/L

Urea nitrogen
66.77
46.04
39
50.99
2.5–7.5 mmol/L

Creatinine
1190
756
853
811
60–110 μmol/L

Sodium
122
141
120.5
128.1
135–145 mmol/L

Potassium
4.88
2.44
3.61
3.81
3.5–4.5 mmol/L

Calcium
1.4
1.5
0.92
1.19
2.20–2.55 mmol/L

CPK
2129
2163
3399
1230
<195 UI/L

CPK MB
484.1
481.5
154.8
119
0–24 UI/L

Hemoglobin
8.7
8.2
7.4
6.3
12.3–15.3 g/dL

WBC
3.1
2.86
1.68
1.52
4–10 × 10³/mm³

Platelets
382.0
383.0
249.0
262.0
150.0–450.0 × 10³/mm³

pH
7.10
7.29
7.32
7.38
7.38–7.42

HCO³⁻
5.1
18.2
19.2
18.2
22–26 mmol/L

Anion gap
35.8
25.2
7.21
20.31
16–18 mmol/L

PaO₂
88
91
88
86
95–98 mm Hg

PaCO₂
16.2
26
27
28
40–45 mm Hg

2.1. Toxicological Analyses

Samples of the herbal decoction were obtained from the patient’s wife. It was a dark brown suspension with fine brown deposit and a clear supernatant. It smelled a strong penetrating odor. Samples of both Rhamnus alaternus root and its decoction were sent to be analyzed in the Laboratory of Toxicology in the Center for Emergency Medical Assistance of Tunis in Tunisia.

2.2. Extraction Procedures

After the authenticity and the botanical identification of the species were confirmed according to the “Flore de la Tunisie” [6] phytochemical compounds were extracted from the medicinal decoction using routine methods including liquid-liquid extraction procedures with further analysis by gas chromatography/mass spectrometry (GC-MS). The solvents used were dichloromethane, ethyl acetate, and chloroform at different pH values (1.0, 7.0, and 9.0). The different extracts were dehydrated over anhydrous sulfate. The dry residue was diluted with 2 milliliters of ethyl acetate. One or 2 μL was analyzed by GC-MS. Dried roots of “Rhamnus alaternus” were reduced to small fragments and macerated in a water-methanol mixture (1 : 2) during 4 h with magnetic stirring. 24 hours later, the extract was filtered and the alcoholic layer was evaporated. The aqueous layer was collected in a separating funnel and had been alkalinized by the addition of ammonia (NH₄OH) and then extracted with dichloromethane by liquid-liquid extraction procedures. The organic phase was dehydrated over anhydrous sulfate and concentrated to 1 mL and then analyzed by GC-MS.

2.3. Chromatographic Conditions

The gas chromatograph-mass spectrometer used was a Hewlett Packard 5890-II (Agilent Technologies) fitted with a manual injector and HP5-MS (0.25-μm) capillary column (30 m long and 0.25 mm i.d.). The injection volume was 2 μL; the compounds were separated with helium (carrier gas) at a flow rate of 1 mL/min. The operating conditions were as follows: the injector was programmed to 250°C at 10°C·s⁻¹ and held for 2 min. The oven was programmed from 50°C (2 min) to 100°C at 25°C·min⁻¹ and then to 200°C at 10°C·min⁻¹ (2 min). MS detection was achieved in scan mode for qualitative analysis. Run time was 16 min.

3. Results

Screening by GC-MS of both Rhamnus alaternus roots and infusion extracts revealed the presence of anthraquinone glycosides such as 4,5-dihydroxy-9,10-dioxoanthracène-2-carboxylic acid (rhein), 1,8-dihydroxy-3-(hydroxymethyl)-9,10-anthracenedione (aloe-emodin), and 1,8-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione (physcion). The retention times were 8.95, 9.67, and 10.25 min, respectively (Figure 1).

Figure 1: Original chromatogram of herbal tea extract (scan mode).

Anthraquinone glycosides were detected in a dichloromethane extract and ethyl acetate extract at pH value = 9 and only in a dichloromethane extract at pH value = 7 by GC-MS analysis (Table 2).

Table 2: Qualitative screening by gas chromatography-mass spectrometry (GC-MS).

Dichloromethane extract
Ethyl acetate extract
Chloroform extract

pH = 1
pH = 7
pH = 9
pH = 1
pH = 7
pH = 9
pH = 1
pH = 7
pH = 9

Rhein
ND
+
+
ND
ND
+
ND
ND
ND

Physcion
ND
+
+
ND
ND
+
ND
ND
ND

Aloe-emodin
ND
+
+
ND
ND
+
ND
ND
ND

+: detected; ND: not detected.

4. Discussion

Blood chemistry tests performed before dialysis revealed renal nitrogen retention (serum creatinine of 1190 μmol/L and blood urea nitrogen of 66 mmol/L). Moreover, normochromic and normocytic anemia, hypocalcemia, and the loss of corticomedullary differentiation observed in our patient suggest a chronic renal insufficiency. From a biochemical point of view, major hyperglycemia (14.44 mmol/L) could be one of the underlying factors, which lead to the diagnosis of diabetic nephropathy. According to authors, this nephropathy was most likely aggravated by the potential toxic effect of anthraquinone glycosides found in Rhamnus alaternus infusion extract. Anthraquinones are a group of functionally diverse chemicals structurally related to anthracene, known to be present in the roots and bark of numerous plants of the genus Rhamnus such as senna, cascara, aloe, frangula, and rhubarb used for their laxative properties [7].

Anthraquinone glycosides including emodin, physcion, aloe-emodin, rhein, and chrysophanol are nowadays well recognized as important biologically active components (Figure 2) [8]. Recently, it was reported that anthraquinones exert a wide range of biological activities including antifungal, antimicrobial, and anticancer properties other than the well-known laxative action on the gastrointestinal apparatus [9–11]. Besides health benefits of anthraquinones, it was also reported that they have a cell toxicity effect. In fact, a study exploring anthraquinones toxicity on Sprague Dawley (S.D.) rats showed that the oral administration of these compounds for 13 weeks induced nephrotoxicity as renal tubule epithelial cells swelled and denatured in tissue slice examination. Anthraquinones were responsible for the activation of mitogen activator protein kinase (MAPK), which causes the arrest of cellular cycle, inhibits epithelial cells proliferation, and contributes to nephrotoxicity [12].

Figure 2: Chemical structure of anthraquinone glycosides [5].

Moreover, investigations revealed increased levels of serum CPK 2129 UI/L, hyperkaliemia of 4.88 mmol/L, and widespread muscle pain on the physical examination, which constitute the diagnostic hallmark of rhabdomyolysis [13]. In the present case, rhabdomyolysis did not have an obvious explanation; there was no ischemia, trauma, or drug intake that could explain it. Nevertheless, we know that one of the rare causes of rhabdomyolysis is metabolic disorders; rhabdomyolysis has been described in chronic hypophosphatemia and hyponatremia, and the most common cause is chronic hypokalemia as it can be seen during treatment with diuretics, in hyperemesis gravidarum or during acute diarrhea episodes [14–17].

In the reported case, the patient has experienced an episode of acute diarrhea one week before his admission to the hospital; rhabdomyolysis could be related to a severe hypokalemia that results from the rapid loss of extracellular potassium losses via gastrointestinal route. In fact anthraquinone glycosides have a strong potential to deplete potassium by stimulating the intestinal secretion of water and electrolytes (K⁺, Na⁺, Cl⁻, etc.) [18], and these glycosides are poorly absorbed from the gastrointestinal tract but are cleaved by gut bacteria to produce aglycones that are more readily absorbed and are responsible for the purgative properties of herb-based stimulant preparations [19].

Long-term therapy with anthraquinone glycosides can alter the body’s normal balance of fluids and minerals, which can cause dehydration, severe hypokalemia hyponatremia, asthenia, and anorexia [20, 21]. In addition, lysis of muscle cells releases toxic intracellular components in the systemic circulation that leads to electrolyte disturbances, hypovolemia, metabolic acidosis, and acute renal failure [22, 23]. The patient experienced the same symptoms when he was admitted to hospital except hypokalemia, and the patient has hyperkaliemia because of rhabdomyolysis and the release of intracellular potassium into the plasma. Furthermore, the destruction of muscle cells results in the creation of a “third space” where substantial amounts of water and Na⁺ are concentrated [24, 25], causing hypovolemia and acute renal failure. Organic and phosphoric acids released from the muscle cell lead to metabolic acidosis and increase the anion gap due to the overproduction of organic acids [26].

In summary, the patient who refused to take any medication to control his blood glucose levels except herbal medication has an undiagnosed diabetic nephropathy aggravated by acute renal dysfunction and rhabdomyolysis. All metabolic disorders are mainly imputed to the toxic effects of the anthraquinone glycosides. We noticed that patient completely recovered and symptoms regressed completely when stopping herbal infusion ingestion. Blood chemistry tests performed after dialysis were all normal.

5. Conclusion

Rhamnus alaternus can be toxic when used in an abusive way beside its strong antibacterial, antioxidant, and antidiabetic activities. To our knowledge, this is the first report of a case of renal failure and rhabdomyolysis which is possibly associated with a chronic consumption of Rhamnus alaternus roots. We present this case to illustrate the role of both clinical and biological investigations in handling cases of herbal poisonings. We aimed also to increase awareness among emergency physicians about patients presenting to the Emergency Department with unexplained symptoms (renal failure, rhabdomyolysis, etc.) requiring prompt diagnosis so that such life-threatening complications can be avoided.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

J. Miralles, J. J. Martínez-Sánchez, J. A. Franco, and S. Bañón, “Rhamnus alaternus growth under four simulated shade environments: morphological, anatomical and physiological responses,” Scientia Horticulturae, vol. 127, no. 4, pp. 562–570, 2011.

R. R. Paris and H. Moyse, Matières Médicales Tome II, Masson et Cie, Paris, France, 1967.

R. B. Ammar, W. Bhouri, M. B. Sghaier et al., “Antioxidant and free radical-scavenging properties of three flavonoids isolated from the leaves of Rhamnus alaternus L. (Rhamnaceae): a structure-activity relationship study,” Food Chemistry, vol. 116, no. 1, pp. 258–264, 2009.

R. B. Ammar, I. Bouhlel, K. Valenti et al., “Transcriptional response of genes involved in cell defense system in human cells stressed by H₂O₂ and pre-treated with (Tunisian) Rhamnus alaternus extracts: combination with polyphenolic compounds and classic in vitro assays,” Chemico-Biological Interactions, vol. 168, no. 3, pp. 171–183, 2007.

P. Panichayupakaranant, A. Sakunpak, and A. Sakunphueak, “Quantitative HPLC determination and extraction of anthraquinones in Senna alata leaves,” Journal of Chromatographic Science, vol. 47, no. 3, pp. 197–200, 2009.

G. Pottier-Alapetite, Flore de la Tunisie Angiospermes-Dicotylédones, Imprimerie Officielle de la République Tunisienne, 1979.

E. M. Clementi and F. Misiti, “Potential health benefits of rhubarb,” in Promoting Health, R. R. Watson and V. R. Preedy, Eds., pp. 407–423, 2010.

M. Locatelli, F. Tammaro, L. Menghini, G. Carlucci, F. Epifano, and S. Genovese, “Anthraquinone profile and chemical fingerprint of Rhamnus saxatilis L. from Italy,” Phytochemistry Letters, vol. 2, no. 4, pp. 223–226, 2009.

M. Locatelli, S. Genovese, G. Carlucci, D. Kremer, M. Randic, and F. Epifano, “Development and application of high-performance liquid chromatography for the study of two new oxyprenylated anthraquinones produced by Rhamnus species,” Journal of Chromatography A, vol. 1225, pp. 113–120, 2012.

H. Matsuda, T. Morikawa, I. Toguchida, J.-Y. Park, S. Harima, and M. Yoshikawa, “Antioxidant constituents from rhubarb: structural requirements of stilbenes for the activity and structures of two new anthraquinone glucosides,” Bioorganic and Medicinal Chemistry, vol. 9, no. 1, pp. 41–50, 2001.

S. K. Agarwal, S. S. Singh, S. Verma, and S. Kumar, “Antifungal activity of anthraquinone derivatives from Rheum emodi,” Journal of Ethnopharmacology, vol. 72, no. 1-2, pp. 43–46, 2000.

M. Yan, L.-Y. Zhang, L.-X. Sun, Z.-Z. Jiang, and X.-H. Xiao, “Nephrotoxicity study of total rhubarb anthraquinones on Sprague Dawley rats using DNA microarrays,” Journal of Ethnopharmacology, vol. 107, no. 2, pp. 308–311, 2006.

P. A. Gabow, W. D. Kaehny, and S. P. Kelleher, “The spectrum of rhabdomyolysis,” Medicine, vol. 61, no. 3, pp. 141–152, 1982.

T. Zenone and Q. Blanc, “Rhabdomyolysis with major hypokalemia secondary to chronic glycyrrhizic acid ingestion,” La Revue de Médecine Interne, vol. 30, no. 1, pp. 78–80, 2009.

L. M. Criddle, “Rhabdomyolysis. Pathophysiology, recognition, and management,” Critical Care Nurse, vol. 23, no. 6, pp. 14–22, 2003.

A. L. Huerta-Alardín, J. Varon, and P. E. Marik, “Bench-to-bedside review: rhabdomyolysis—an overview for clinicians,” Critical Care, vol. 9, no. 2, pp. 158–169, 2005.

A. Chubachi, H. Wakui, K. Asakura, S. Nishimura, Y. Nakamoto, and A. B. Miura, “Acute renal failure following hypokalemic rhabdomyolysis due to chronic glycyrrhizic acid administration,” Internal Medicine, vol. 31, no. 5, pp. 708–711, 1992.

P. M. Copeland, “Renal failure associated with laxative abuse,” Psychotherapy and Psychosomatics, vol. 62, no. 3-4, pp. 200–202, 1994.

National Toxicology Program, “NTP toxicology and carcinogenesis studies of EMODIN (CAS NO. 518-82-1) feed studies in F344/N rats and B6C3F1 mice,” National Toxicology Program Technical Report Series 493, 2001.

M. Moulin and A. Coquerel, Pharmacologie, Masson, Paris, France, 2nd edition, 2002.

J. Kienlen, “Rhabdomyolyse,” in Congrès National d'Anesthésie et de Réanimation, Les Essentiels, pp. 469–476, 2007.

L. Criddle, “Rhabdomyoysis. Pathophysiology, recognision, and management,” Critical Care Nurse, vol. 23, no. 6, pp. 14–32, 2003.

B. Dussol, “Equilibre potassique, hypokaliémie et hyperkaliémie,” Néphrologie et Thérapeutique, vol. 6, no. 3, pp. 180–199, 2010.

D. Singh, V. Chander, and K. Chopra, “Rhabdomyolysis,” Methods and Findings in Experimental and Clinical Pharmacology, vol. 27, no. 1, pp. 39–48, 2005.

D. J. Malinoski, M. S. Slater, and R. J. Mullins, “Crush injury and rhabdomyolysis,” Critical Care Clinics, vol. 20, no. 1, pp. 171–192, 2004.

T. A. Rusell, “Acute renal failure related to rhabdomyolysis: pathophysiology, diagnosis and collaborative management,” Nephrology Nursing Journal, vol. 27, no. 6, pp. 567–577, 2000.