International Journal of Food and Nutritional Science

Nephropathy is a microvascular complication of anti-tuberculosis therapy that can disturb treatment and cause permanent kidney damage.The current study was designed to evaluate the possible protective effects of Prunus armeniaca leaves extract against isoniazid (INH) and rifampicin (RIF)-induced nephrotoxicity in rats. The experimental rats received INH and RIF at dose level of 50 mg/kg, and either 100 mg or 200 mg/kg body weight Prunus armeniaca leaves extract orally for 45 days. INH/ RIF administration induced nephrotoxicity evidenced by the histopathological alterations as well as significant (P<0.001) increase in serum urea, creatinine and uric acid. INH/RIF-intoxicated rats exhibited a significant increase in serum tumor necrosis factor alpha (P<0.01) and renal lipid peroxidation levels (P<0.001). Conversely, reduced glutathione content, and activity of superoxide dismutase and glutathione peroxidase were significantly declined in kidney of INH/RIF-induced rats. Concomitant supplementation with either dose of Prunus armeniaca leaves extract prevented the INH/RIF-induced biochemical and histopathological alterations. In conclusion, the present study confers new information on the protective effect of Prunus armeniaca leaves extract against anti-tuberculosis therapy-induced nephrotoxicity. Prunus armeniaca protect against INH/RIF-induced renal injury through abolishment of inflammation and oxidative stress, and potentiation of the antioxidant defense system. *Corresponding Author: Mahmoud, A.M. Department of Zoology, Physiology Division, Faculty of Science, Beni-Suef University, Beni-Suef, Egypt. Tel: +201144168280; E-mail: ayman.mahmoud@science.bsu.edu.eg Received Date: Aug 10, 2015 Accepted Date: Sep 01, 2015 Published Date: Sep 05, 2015


Introduction
Tuberculosis (TB), a serious disease caused by Mycobacterium tuberculosis, is a growing international health concern [1] . It primarily affects lungs and secondarily other organs of the body [2] . The standard treatment of TB consists of a six to nine months course of antibiotics including isoniazid (INH), rifampicin (RIF), pyrazinamide (PZA) and ethambutol or streptomycin [3] . It has been reported that the use of isoniazid and its combination with rifampicin is associated with liver damage that could result in acute liver failure with a high mortality rate [4,5] . The rate of their hepatotoxicity is much higher in developing countries compared to that in developed countries, even with using the same dose schedule [6] . Although the hepatotoxic effects of the anti-tuberculosis drugs have been extensively studied, their induced nephrotoxicity have been poorly documented. The study of Mahmoud et al. [5] demonstrated that oxidative stress is implicated in the INH-induced toxicity in rats. In addition, Lopez-Novoaet al. [7] reported that reactive oxygen species (ROS) and oxidative stress represent the central key in the pathogenesis of drug-induced renal damage. Therefore, the use of antioxidants could offer protection against drug-induced renal damage.
Currently, medicinal plants are widely used in the treatment of many diseases owing their safety, cheapness and nontoxicity when compared with the synthetic drugs [8] . It has been estimated that about 80% of the world population relies on natural and botanical preparations as medicine to meet their health needs [9] . Also, the dietary intake of carotenoids, vitamins and flavonoids, which are widely dis-tributed in plants, could be useful in protecting against drug-induced nephrotoxicity [10] . Prunus armeniaca L. (apricot) is a fruit that has a high content of carotenoids [11] , vitamins and selenium [12] . Since apricot contains β-carotene, polyphenols, flavonoids, and vitamins which are well-known antioxidants, there is a foundation for assuming that it may have strong antioxidant properties [13] , and could protect against drug-induced oxidative stress. The fruits of Prunus armeniaca have been well studied in terms of their antioxidant and nephroprotective effects. However, the protective effects of the leaves extract against nephrotoxicity associated with the use of anti-tuberculosis drugs have not been documented. Therefore, the present study was designed to evaluate the protective effects of Prunus armeniaca leaves extract against INH and RIF-induced renal injury in rats.

Chemicals
INH was purchased from El Nasr Company for Chemicals and Drugs (Cairo, Egypt) and RIF was supplied by Novartis Pharma Company (Cairo, Egypt). Glutathione (GSH), pyrogallol, thiobarbituric acid (TBA) and 5,5'-dithiobis-(2-nitrobenzoic acid) (DTNB) were purchased from Sigma (USA). All other chemicals were of analytical grade and obtained from standard commercial supplies.

Preparation of Prunus armeniaca Leaves Extract
Leaves of Prunus armeniaca were collected from Alfayoum (Egypt). The samples were identified by a plant Taxonomist, and the plant leaves were air-dried in shade and separately ground to a fine powder. The powdered materials were extracted by maceration in 80% aqueous ethanol until exhaustion at room temperature. 100 g of each sample was soaked in 1 L of solvent with sonication at room temperature for 24 h. After filtration, the filtrate was concentrated under reduced pressure in a rotary evaporator. The crude extracts were weighted and stored at -20°C till used. The extract was subjected to tests for detection of the presence of tannins, alkaloids, carbohydrates and/or glycosides, and/or nitrogenous bases, flavonoids, saponins, unsaturated sterols and triterpenes [14] .

Experimental Animals and Treatments
Twenty-four male Wistar rats weighing 100-120 g were used as experimental animals in the present investigation. They were obtained from the animal house of Research Institute of Ophthalmology, El-Giza, Egypt. They were kept under observation for about 10 days before the onset of the experiment to exclude any intercurrent infection. The chosen animals were housed in plastic cages with good aerated covers at normal atmospheric temperature (25 ± 2°C) and normal 12 h light/dark cycle. Rats were received water and standard balanced diet ad libitum. All animal procedures were undertaken with the approval of Institutional Animal Ethics Committee of Beni-Suef University (Egypt).
Rats were divided to four groups (N = 6) and were subjected to the following treatments: Group 1 (Control): Served as control and were orally administered the vehicle 1% carboxymethylcellulose (CMC) for 45 days. The doses of INH, RIF and Prunus armeniaca were balanced consistently as indicated by any change in body weight over the entire period of study. By the end of the experiment, animals were sacrificed under ether anesthesia and blood samples were collected, left to coagulate and centrifuged at 3000 rpm for 15 min to separate serum. Kidney samples were immediately excised and perfused with ice-cold saline. Frozen samples (10% w/v) were homogenized in chilled saline and the homogenates were centrifuged at 3000 rpm for 10 min. The clear homogenates were collected and used for subsequent assays. Other kidney samples were fixed in 10% buffered formalin for histological processing.

Biochemical Assays Determination of Serum Urea, Creatinine and Uric Acid:
Serum urea, creatinine and uric acid levels were assayed using reagent kits purchased from Biosystems (Spain), following the methods of Kaplan [15] , Young [16] and Fossati et al. [17] , respectively.

Determination of Serum Tumor Necrosis Factor-alpha (TNF-α):
Serum levels of TNF-α were determined by specific ELISA kits purchased from R&D Systems (USA), according to the manufacturer's instructions. The concentration of TNF-α was determined spectrophotometrically at 450 nm. Standard plot was constructed by using standard cytokine and the concentrations for unknown samples were calculated from the standard plot ( Figure 1).

Determination of Oxidative Stress and Antioxidant System
Parameters: Lipid peroxidation, assayed as malondialdehyde (MDA), was determined in kidney homogenates according to the Int J Food Nutr Sci | Volume 2: Issue 2 www.ommegaonline.org Nephroprotective effect of apricot leaves extract method of Preuss et al. [18] . Reduced glutathione (GSH) content was assayed according to the method of Beutler et al. [19] . Activities of superoxide dismutase (SOD) and glutathione peroxidase (GPx) were measured according to the methods of Marklund [20] and Matkovics et al. [21] , respectively.
Histopathological Study: The kidney samples were flushed with cold saline and then fixed in 10% buffered formalin for at least 24 h. The specimens were then dehydrated in ascending series of ethanol, cleared in xylene and embedded in paraffin wax. Blocks were prepared and 4 μm thick sections were cut by a sledge microtome. The paraffin embedded sections were deparaffinized, washed and stained with hematoxylin and eosin (H&E). The stained slides were examined under light microscope.
Statistical Analysis: Statistical analysis was performed using GraphPad Prism 5 software (GraphPad Software, San Diego, CA, USA). Results were expressed as mean ± standard error (SEM) and all statistical comparisons were made by means of the one-way ANOVA test followed by Tukey's test post hocanalysis. A P value <0.05 was considered significant.

Results
Qualitative phytochemical screening revealed the presence of carbohydrates and/or glycosides, tannins, flavonoids, coumarins and triterpenes in the leaves extract of Prunus armeniaca (Table 1).  Table 2

Discussion
Kidney injury is a severe complication that can disturb treatment and cause permanent kidney damage [22] . It has been reported that nephropathy is an important microvascular complication of anti-tuberculosis therapy [23] . Multiple studies have reported that oxidative stress and inflammation are implicated in drug-induced organ toxicity [5,24] . However, renal injury induced by anti-tuberculosis therapy is usually reversible and could be treated appropriately if detected early [23] . Therefore, the use of antioxidants could protect against INH/RIF-induced oxidative stress and nephrotoxicity. We designed the current study to test the hypothesis that Prunus armeniaca leaves extract could protect against INH/RIF-induced renal damage in rats through attenuation of inflammation and prevention of oxidative stress.
The present findings showed that the administration of INH and RIF has induced renal injury and glomerular dysfunction as evident by the elevated serum urea, creatinine and uric acid levels. These parameters are often regarded as reliable markers of renal damage [25] . In addition, serum creatinine has been used to estimate glomerular function and its elevation is an indicator of renal failure [26] . The elevated serum markers of renal Int J Food Nutr Sci | Volume 2: Issue 2 www.ommegaonline.org Nephroprotective effect of apricot leaves extract toxicity markers is in agreement with the study of Hashmi et al. [27] who reported increased serum levels of urea and creatinine in albino rabbits following administration of anti-tuberculosis drugs. INH/RIF-induced nephrotoxicity was further confirmed by the observed histological alterations such as atrophy of glomerular tuft, inflammatory cells infiltration and dysplastic renal tubules. Concomitant administration of either dose of Prunus armeniaca markedly decreased serum levels of urea, creatinine and uric acid, and potentially prevented the induced histological alterations in the kidney.
TNFα, a potent pro-inflammatory cytokine, is an important mediator of inflammatory tissue damage. It has been well documented that the immune system contributes to drug-induced nephrotoxicity, and several studies presented evidence that nephrotoxicants could induce an inflammatory response leading to organ injury [28] . INH/RIF administered rats exhibited a marked increase in serum levels of TNFα, reflecting the degree of inflammation. These findings are in agreement with our recent study where we reported a significant increase in serum levels of pro-inflammatory cytokines in INH-induced rats [5] . On the other hand, concurrent administration of 100 and 200 mg Prunus armeniaca leaves extract produced pronounced decline in serum TNFα, indicating its anti-inflammatory efficacy. In this context, Bhattacharjee et al. [29] demonstrated the anti-inflammatory activity of Prunus persica leaves extract in Wistar rats.
ROS and oxidative stress have been implicated in the pathogenesis of drug-induced renal damage [7] . Long chain polyunsaturated fatty acids are abundant in the composition of renal lipids and this makes the kidney vulnerable to damage caused by ROS [30] . ROS have the ability to induce lipid peroxidation, protein damage, cellular injury, DNA fragmentation and alter the antioxidant defense system [31] . In the present study, INH/ RIF administration significantly increased the lipid peroxidation marker MDA, revealing a serious damage to kidney tissue. Daily treatment with Prunus armeniaca leaves extract markedly decreased the elevated levels of MDA, suggesting evidence that the used treatment possess a potent free radical scavenging activity. Conversely, INH/RIF-administered rats exhibited significantly declined renal GSH content as well as activity of the antioxidant enzymes SOD and GPx. GSH is a potent antioxidant which forms S-conjugates with products of lipid peroxidation [32] and thus protects the cellular constituents. As well, SOD and GPx play a key role in protecting the body against the deleterious effects of ROS [33] . Recently, we reported that INH administration produced significant increase in MDA and NO, and marked decrease in the antioxidant defenses in rats [5] . Concurrent administration of Prunus armeniaca leaves extract markedly decreased lipid peroxidation and alleviated renal GSH content as well as activity of the antioxidant enzymes. Therefore, we assume that the nephroprotective mechanism of Prunus armeniaca against INH/RIF-induced oxidative stress is partially mediated through prevention of GSH decline and potentiation of the enzymatic antioxidant defenses. In addition, these findings provide evidence on the free radical scavenging and antioxidant activity of Prunus armeniaca leaves extract which could be attributed to the presence of active constituents of well-known antioxidant efficacy such as flavonoids, tannins and terpenoids. Previous studies demonstrated the nephroprotective effects of Prunus armeniaca fruit in radiation [34] and methotrexate-induced [35] kidney damage connected its protective effect to the presence of constituents Int J Food Nutr Sci | Volume 2: Issue 2 such as flavonoids.
In conclusion, the present study confers new information on the protective effect of Prunus armeniaca leaves extract against anti-tuberculosis therapy-induced nephrotoxicity. Although the nephroprotective effect of Prunus armeniaca fruit has been well demonstrated, this is the first report evaluated the protective effect of its leave extract against INH/RIF-induced renal injury in rat. This renoprotective effect could be explained through the ability of Prunus armeniaca to attenuate the pro-inflammatory cytokine production, inhibit lipid peroxidative system, prevent GSH decline and enhance the enzymatic antioxidants. However, further studies are required to trace out its exact mechanistic pathways.