Pharmacognosy Magazine

ORIGINAL ARTICLE
Year
: 2022  |  Volume : 18  |  Issue : 77  |  Page : 152--159

Protective effect of Lycium barbarum on renal injury induced by acute pancreatitis in rats


Tugba Dogan1, Kadir Batcioglu1, Elif Kayhan Kustepe2, Ayse Burcin Uyumlu1, Yakup Yilmaztekin1,  
1 Department of Biochemistry, Faculty of Pharmacy, İnonu University, Malatya, Turkey
2 Department of Histology and Embryology; Department of Basic Medical Sciences, Faculty of Medicine, İnonu University, Malatya, Turkey

Correspondence Address:
Kadir Batcioglu
Department of Biochemistry, Faculty of Pharmacy, İnonu University, Battalgazi, Malatya
Turkey

Abstract

Background: Lycium barbarum (LB) is a plant species that is well known in Chinese traditional medicine and is also considered a nutrient, belonging to the Solanaceae family, also called goji berry or wolfberry. Objectives: The aim of this study was to investigate the protective efficacy of LB, in kidney damage caused by acute pancreatitis (AP). Materials and Methods: In the study, we used 36 female Wistar albino rats (12 in each group) which were divided into three groups: Control, cerulein (100 μg/kg b. wt. intraperitonally) and Cerulein + LB (6 mg/ml/day gastric gavage) group. Serum lipase, Interleukin (IL)-1, and IL-6 levels were measured. Superoxide dismutase, catalase (CAT), glutathione peroxidase enzyme activity assays and 8-hydroxy deoxyguanosine, malondialdehyde (MDA), and protein levels were measured in kidney tissue samples. In addition, histopathological analysis was performed in kidney tissue samples. Results: According to the findings, in the AP model created with Cerulein, administration of LB plant extract decreased oxidative stress and damage caused by AP in the kidney tissue and partially suppressed the inflammatory reactions in the tissue. Conclusion: According to the findings, in the AP model created with Cerulein, administration of LB extract decreased oxidative stress and in kidney damage caused by AP.



How to cite this article:
Dogan T, Batcioglu K, Kustepe EK, Uyumlu AB, Yilmaztekin Y. Protective effect of Lycium barbarum on renal injury induced by acute pancreatitis in rats.Phcog Mag 2022;18:152-159


How to cite this URL:
Dogan T, Batcioglu K, Kustepe EK, Uyumlu AB, Yilmaztekin Y. Protective effect of Lycium barbarum on renal injury induced by acute pancreatitis in rats. Phcog Mag [serial online] 2022 [cited 2022 Dec 6 ];18:152-159
Available from: http://www.phcog.com/text.asp?2022/18/77/152/341077


Full Text



SUMMARY

In the cerulein-induced acute pancreatitis model, administration of Lycium barbarum plant extract showed a partial suppressive effect on inflammatory reactions in the tissue by reducing the oxidative stress and damage caused by acute pancreatitis.

[INLINE:1]

Abbreviations used: LB: Lycium barbarum, AP: Acute pancreatitis, IL: Interleukin, TNF α: Tumor necrosis factor alpha, MDA: Malondialdehyde, CAT: Catalase, GSHPx: Glutathione peroxidase, SOD: Superoxide Dismutase, 8-OHdG: 8-hydroxydeoxyguanosine, ROS: Reactive oxygen species.

 Introduction



Acute pancreatitis (AP) occurs as a result of the development of a widespread inflammation as a result of digestive enzymes, which are normally inactive in the pancreas, digest pancreatic tissues as an early activity with an etiological factor whose cause is not yet known.[1] Due to severe inflammation in the pancreas, adjacent and distant organs of the pancreas also occurs damage in different intensities. The kidney, liver, spleen, and lungs are firstly among these organs.[2] Although the etiological factors that cause AP show a lot of variety, the clinical picture that occurs whatever happens of the etiological factor is characterized by the self-digestion of the tissue (autodigestion) with the activation of enzymes in the pancreas, and the inflammation, edema, hemorrhage and necrosis that develop accordingly.[3]

Cytokines such as interleukin (IL)-1 and IL-6 are released from activated cells. AP is transformed from a local inflammatory process to a disease showing systemic effects through these inflammation mediators.[4] Pancreatic necrosis, multiple organ failure, and mortality are seen commonly in this disease, which can cause cardiovascular, pulmonary, and renal failure in the early period and septic problems in the late period.[5],[6],[7]

Renal dysfunction is among the serious complications of AP. The picture, which is seen in 80% of the patients and named “Nephropathia Pancreatica” by Otto, is characterized by proteinuria and hematuria. It has been reported that 23% of patients who develop acute renal failure depend on AP, and the mortality rate in these patients is about 80%. Acute tubular necrosis has been associated with the severity of pancreatic inflammation. If the hemodynamic changes occurring in AP are not corrected with appropriate treatment in a short time, renal dysfunctions develop. The development of septic complications also plays a role in the etiology of renal dysfunction.[8]

In many studies in the literature, it has been reported that the degenerative effects of cytokines such as IL-1, IL-6, and tumor necrosis factor-alpha (TNF-α), whose concentrations increase in the systemic circulation as a result of inflammation developing in the etiology of renal damage. In addition, early activated pancreatic-derived proteases and lipases and oxidative damage caused by free oxygen radicals play a role in this process. Due to these interrelated factors, the process becomes extremely complicated.[9],[10],[11]

Oxidative stress plays a critical role in the initial and progression stages of AP, as in many diseases. Many experimental models have been put forward to support the accuracy of this approach.[12],[13],[14],[15] Free oxygen radicals (reactive oxygen species [ROS]) and cytokines are take place in the center of the molecular mechanism in the development of progressive hemorrhagic necrosis that occurs in the early stages of AP.[16],[17],[18] There is a dynamic balance between ROS, which is continuously produced in the organism under physiological conditions, and antioxidant defense systems, and therefore harmful effects do not occur. However, in AP, reactive oxygen radicals, whose concentrations increase with severe inflammation that develops suddenly and rapidly, disrupting the balance in favor of oxidants, create severe oxidative stress.[15],[19],[20]

Lycium barbarum (LB) is a plant species that is well known in Chinese traditional medicine and is also considered a nutrient, belonging to the Solanaceae family, also called goji berry or wolfberry. This plant is up to 3 meters tall, its leaves are gray-green, its petiole is very short and there are 1–3 flowers on each branch. Fruits are 3–8 mm in diameter, 6–20 mm in length, and have a dark red color. Its role in preventing various diseases has been demonstrated many times in experimental, clinical, and epidemiological studies.[21],[22] The important bioactive ingredients of LB are complex glycoconjugates with glycoprotein structure. It contains a peptide structure consisting of 6 monosaccharides (galactose, glucose, rhamnose, arabinose, mannose, and xylose) and 18 amino acids. Oligosaccharides, which are one of the main components in its structure, show efficiency in cell–cell interaction and adhesion, cell migration, blood coagulation, immune response, and wound healing, and these activities are some of their many known functions.[23],[24],[25] LB contains many bioactive vitamins (Vitamin A, B1, B2, C), carotenoids (zeaxanthin, lutein, lycopene, cryptoxanthin), cerebroside, β-sitosterol, proline, scoleptin, and betaine, which are known to have strong antioxidant effects.

It has been reported that LB shows anti-inflammatory, antineoplastic, antipyretic, antidiabetic, antisenyl, immunomodulatory, and antiaging effects due to this rich content.[26],[27],[28],[29],[30]

Although it is known that barbarum suppresses inflammation and increases antioxidant capacity in AP,[31],[32],[33],[34] no study investigating its effectiveness against nonpancreatic organ damage has been found. In this study, we investigated whether LB extract has a protective effect against renal injury in rats with experimentally induced AP by cerulein.

 Materials and Methods



Reagents and chemicals

Sodium Carbonate (≥99.9%), Nitro Blue tetrazolium Chloride (≥90.0%), 2-(2-Thiobarbituric acid) (≥98%), Acetic Acid (≥99%), Sodium azide (≥99.5%), n-Butanol (99.8%), and Sodium Carbonate (≥99.9%) were acquired from Merck Chemicals, USA. Sodium Potassium Tartrate (99%), Sodium Hydroxide (98%–100.5%), Copper Sulphate pentahyrate (98.0%), Folin-Ciocalteu-Phenol Reagent, Xanthine (≥99%), Ethylenediaminetetraacetic acid (99%), Bovine serum albumin (BSA) (≥98%), Hydrogen peroxide (30%), Sodium Dodecyl Sulfate (≥99.0%), NADPH-(=97%), Tris hydrochloride (>99%), Ethanol (≥99.8%), Proteinase K (≥90%), RNase T1, RNase A (≥95%), Nuclease P1, Alkaline phosphatase, Acetonitrile (99.8%), Sodium Acetate (≥99%), Glutathione (>98%), and Cerulein (≥95%) were acquired from Sigma-Aldrich Chemicals, USA.

Rat IL-1 β (BMS630TEN) and Rat IL-6 (BMS625TEN) Elisa Kits were obtained from eBioscience ELISA Kits, Thermo Fisher Scientific, USA. Quanti chrome lipase kit was obtained from BioAssay Systems, USA.

Design of study

This study was carried out in Inonu University Turgut Ozal Medical Center, in the Experimental Research Unit, by the rules stipulated by the Inonu University animal ethics committee (Research protocol number: 2011/A-16). 36 female Wistar albino rats, 3–4-month old, with an average weight of 250–300 g were used. During the study, all animals were kept in polypropylene cages (4 animals were kept at each cage) and fed ad libitum standard feed and tap water. 12 h light/12 h dark period was applied and the room temperature was hold of 22°C–24°C.

A total of 36 female rats were divided into 3 groups randomly selected with 12 animals in each group.

Group 1: The control group was made only saline physiological injection was used as a solvent during the study and fed with ad libitum standard feed and water for 10 daysGroup 2: Induction of AP was provided with 50 μg/kg b. wt cerulein applied twice intraperitoneally with a total dose of 100 μg/kg b. wt with 2 h intervals, after giving ad libitum standard feed and water. Saline was used as a solvent[35]Group 3: 10 days before cerulein injection LB extract was given by i.g., gavage method at a dose of 6 mg/ml/day for 10 days. In this time, it continued to be fed with standard feed and water.[36]

Extraction processes of Lycium barbarum samples

Sun-dried goji berry berries (LB) harvested in Manisa-Turkey and sold in the local market were purchased. Sun-dried LB fruits were pounded in a mortar and pulverized. After taking 10 g of the powdered material and adding 200 mL of methanol-water (v/v, 80:20%) at 60°C, it was mixed with a magnetic stirrer for 1 h. At the end of the process, the mixture was centrifuged at 5000 rpm for 25 min. After the upper liquid part was taken into another tube, 20 mL (80°C) of pure water was added to the tube with the residue and it was centrifuged again at 5000 rpm for 25 min. This process was carried out in 3 repetitions. The extracts collected at the end of each centrifugation were combined. These extracts were evaporated in the evaporator until 25 mL remain. Methanol: water (v/v, 80:20%) was added to this extract until it was completed to 100 mL. Then, the obtained extract was vortexed and kept at 4°C for 10 h, all solvent in the extract was evaporated in the evaporator. The obtained L. barbarum extract powder was dissolved in distilled water to a final concentration of 6 mg/ml and used completely. The yield of LB extract is 5%. The all steps for this extraction procedure are shown in [Figure 1].[37] Dosage adjustment was modified according to the study of Zhao et al. to be administered at 6 mg/kg/day for 10 days.[36]{Figure 1}

Biochemical analysis

At the end of 10-day feeding period, cerulein injections were made and after 24 h rats were sacrificed by cervical dislocation. The rats whose ribcages were opened were blood withdrawn by entering the heart with an injector and kept in closed tubes for 10 min at room temperature and centrifuged at 3500 rpm for 5 min to obtain serum. The separated serum was stored at −40°C for measurement of lipase, IL-1, and IL-6. Both kidneys were taken after sacrification. The right kidney was saved in 10% formaldehyde solution for histopathological examination. The left kidney was used for biochemical measurements.

Preparation of kidney tissues for biochemical analysis

Kidney tissues, which were delivered to the laboratory by cold chain, were transferred to glass tubes and cold 50 mM phosphate buffer (6.059 g of K2HPO4, 2.07 g of KH2PO4 were taken and dissolved in 800 ml of distilled water and the pH was adjusted to 1000 ml) (pH 7.4) was added by creating a 1:10 w/v ratio. It was then homogenized for 5 min at 6000 rpm in the ultra-Turrax T25 (IKA Werke GmbH, Staufen, Germany) homogenizer. The obtained homogenates were sonicated 3 times for 10 s at 20 s intervals using VWR Bronson scientific sonicator (VWR Int. Ltd. Merck House Pool, UK). The supernatant was obtained by centrifuging homogenates at 4°C at 13,500 g for 15 min (Centrifuge 5415R, Eppendorf AG, Hamburg, Germany). The supernatants were stored at −80°C for protein quantity determination, Superoxide dismutase (SOD), CAT, GPx activity determination (SANYO Biomedical Co., Co., MDF-U537, Osaka, Japan). 500 μl of homogenate was used for the measurement of malondialdehyde (MDA) levels.

Measurment of biochemical parameters

Protein levels of samples were measured according to Lowry method and BSA was used as protein standard.[38] MDA levels were measured using thiobarbituric acid reactive substances assay method developed by Mihara and Uchiyama, and the results were expressed in nmol/mg protein.[39]

SOD activity was determined according to the method of McCord and Fridovich. This method is based on the inhibition by SOD of the reduction of cytochrome C through superoxide radicals produced in the xanthine-xanthine oxidase system.[40] Enzyme activities were calculated assuming that 50% inhibition of the reduction of cyt c is equivalent to 1 U of SOD enzyme activity and the results were given as U/mg protein. Pure SOD enzyme was used to draw the standard graph.

Determination of Catalase enzyme activity was made according to the method of Luck H.[41] The decomposition of H2O2 to water and molecular oxygen by the catalytic activity of CAT was monitored spectrophotometrically at 240 nm. Specific activity was expressed in terms of U/mg protein.

GPx activity measurement was made according to the method of Lawrence and Burk.[42] The activity was assayed by following the oxidation of NADPH at 340 nm for 3 min, 25°C, in the presence of Glutathione reductase (GR) and GSH. One unit of activity was defined as oxidation of 1 μmol NADPH per minute. The final GPx activity levels were expressed as U/mg protein.

8-hydroxy deoxyguanosine quantification

DNA isolation

One gram of kidney tissue taken into the test tube was homogenized with a solution containing 10 mL of 1% SDS and 1 mM EDTA in an Ultra-Turrax T25 (IKA Werke GmbH, Staufen, Germany) homogenizer at 6000 rpm for 5 min. Homogenates were incubated with Proteinase K for 30 min at 37°C. After adding 0.5 mL pH 7.4 1 M Tris-HCl, it was extracted with 1 volume of Chloroform: Isoamyl alcohol (24:1, v: v). After the phases were separated by centrifuge, the aqueous phases were collected. DNA was precipitated with 0.1 volume of absolute ethanol kept at −20C. After centrifugation, DNA washed with 70% ethanol was solubilized with 2 ml 1.5 mM NaCl, 150 μM Na-Citrate, and 1 mM EDTA solution. The solution was incubated at 37°C for 30 min with RNase T1 and RNase A. DNA solution was extracted again with chloroform: isoamyl alcohol solution and precipitated with 5 m NaCl.[43]

After dissolving precipitated DNA pellets with 0.5 mL 20 mM CH3COONa, 30 min at 37°C. 60 min at 37°C by incubating with 63 mg nuclease P1 and adding 50 μL 1 m Tris-HCl. 6.3 U was incubated by alkaline phosphatase.[44]

High-performance liquid chromatography analysis

High-performance liquid chromatography (HPLC) analyzes were made with the manual injection Agilent 1100 (Agilent Technologies, Inc., Headquarters, Santa Clara, United States) device. Parts of 20 μL of the isolated DNA samples were loaded into the C18 HPLC column (ACE, Aberdeen, Scotland) with an internal diameter of 4.6 mm with a particle size of 3 μm. The analysis was done isocratically with 0.1% (v: v) acetic acid mobile phase containing 3% (v: v) acetonitrile at a flow rate of 2 ml/min and was carried out at UV 297 nm.[45] It was graphed with the concentration corresponding to the peak areas obtained as a result of analysis of solutions of different concentrations prepared by the 8-hydroxy deoxyguanosine (8-OHdG) standard under the same chromatographic conditions. Using the correct equation of the generated graph, 8-OHdG content of the samples was determined and expressed as nmol/mg DNA.

Measurement of pancreatic lipase level in serum

Pancreatic lipase measurement was performed by the procedure specified in the supplied pancreatic lipase Bioassay Systems' Quanti chrome lipase kit.

Cytokine determination in serum

At the end of the study, IL-1 β and IL-6 levels of the samples taken from all groups were measured using the ELISA method (eBioscience Rat-IL-1 β Platinum ELISA Kit) and the results were calculated in pg/ml with the help of the standard graph.

Histopathological examination of kidney tissue

Kidney tissue samples taken for histological examination were detected for 48 h with 10% formaldehyde. After fixation, kidney tissue samples were embedded in paraffin blocks after a routine histological tissue follow-up procedure. Cross-sections 6 μm thick were prepared with the help of microtomes from paraffin blocks. After sections taken on slides were stained with H and E (H and E), and photographs were taken by examining with Nikon Optichot-2 light microscope and Nikon DS-L3 Camera control-Image analysis system (Nikon Corporation, Tokyo, Japan).[46]

Statistical analyze

One-sample Kolmogorov–Smirnov test was applied first to test whether the data conformed to the normal distribution, and it was observed that the data conformed to the normal distribution. Analysis of variance test was used to compare between groups of data showing compliance with normal distribution and the LSD post hoc test was performed to analyze which parameters belonged to the observed differences between the groups. In all these tests, the statistical significance level was considered to be P < 0.05. All statistical analyses were performed using SPSS (SPSS 15.0 Inc., Chicago, IL, USA).

 Results



Biochemical findings

The results of all parameters obtained in this study are summarized in below in graphs [Figure 2].{Figure 2}

According to the results of antioxidant parameters in our study; SOD and GPx enzyme activity showed a statistically significant decrease in the AP group compared to the control group. On the other hand, LB application showed a significant increase compared to the AP group (P < 0.05). Although there was a certain increase in CAT activity in the AP group compared to the control group, the difference between the groups was not statistically significant but showed a certain increase (P > 0.05). Similarly, although lower CAT levels were determined in the LB group compared to AP group, the difference was not statistically significant (P > 0.05).

Although there was a certain increase in MDA level in the AP group compared to the control, the difference between the groups was not statistically significant (P > 0.05). The LB group decreased in a statistically significant way the MDA level, which was high in both the control and AP groups (P < 0.05). The amount of 8-OHdG did not cause a significant change in the AP group compared to the control. LB group decreased in a statistically significant way the amount of 8-OHdG in both control and AP groups (P < 0.05).

The lipase level we obtained in the study showed a statistically significant increase in the AP group compared to the control group (P < 0.05). In addition, the lipase level in the LB group showed a statistically significant increase compared to both the control and AP groups (P < 0.05).

According to our study findings, IL-1 level showed a significant increase in the AP group compared to the control (P < 0.05). However, the LB group significantly decreased the IL-1 level, which increased depending on the AP group (P < 0.05). There was no statistically significant difference between the 1st and 3rd groups (P > 0.05).

According to our study findings, although a certain increase in IL-6 level was observed in the AP group compared to the control group, the difference between the groups was not statistically significant. LB group decreased in a statistically significantly IL-6 level, which was high in both control and AP groups (P < 0.05).

If we present all biochemical parameters in a single table collectively;

Histopathological examination

The cortical [Figure 3]a and [Figure 3]b and medullary [Figure 3]c structures in the kidney tissue sections in the control group were evaluated as normal histological structure.{Figure 3}

In the cross-sections of the kidneys in the AP group, collapse in the glomeruli commonly, dilatation in the Bowman gap, increase in the density of eosinophilic cytoplasm in distal and proximal tubular epithelial cells, and heterochromatic and pycnotic nucleus structure were noted [Figure 3]c and [Figure 4]a.{Figure 4}

Place-to-place hemorrhage was detected in the renal cortex [Figure 4]b and medulla [Figure 4]c. Distal and proximal tubular degeneration around the hemorrhagic areas in the cortex [Figure 4]b and degeneration of the medullary tubular structures in the regions close to the hemorrhagic areas in the medulla [Figure 4]c were detected.

When the sections in the treatment group were examined, it was observed that there was a significant decrease in the histological findings of kidney damage observed in the AP group. Glomeruli were evaluated in normal appearance. Glomeruli were evaluated in normal appearance. Hemorrhage was not detected in kidney sections in this group. However, there was minimal eosinophilic cytoplasm concentration in proximal and distal tubular epithelial cells [Figure 4]d and [Figure 5]a and damage to in place to place tubular epithelial cells [Figure 5]b.{Figure 5}

 Discussion



AP is an acute inflammatory disease of the pancreas that can affect surrounding tissues and distant organs at varying levels.[47] Acute kidney injury (AKI) occurs in 70% of patients with severe AP, and this complication significantly increases the risk of AP-related mortality.[48] In this study, we investigated whether there is a protective effect of LB plant extract known to have anti-inflammatory and antioxidant-effective ingredients in preventing developing kidney tissue damage linked to AP, which is experimentally created with cerulein in the rats.

With the onset of AP, increases of serum lipase and amylase enzymes released from acinar cells are biomarkers used in biochemical measurements. In a study conducted in humans by Zhou et al., an increase in serum lipase level was observed in patients with severe AP due to the increase in the severity of the disease.[49] In our study, serum lipase level increased significantly (P < 0.05) in the experimental AP group induced with cerulein, but the application of LB extract could not prevent this increase in serum lipase level. This result does not coincide with the study conducted by Xiong et al., which found that in the AP model with cerulein in mice, the administration of LB polysaccharides significantly reduced the level of lipase increased as a result of the formation of AP.[34]

It has been reported in several studies that LB has anti-inflammatory activity alongside its antioxidant effect.[50],[51] LB extract has been observed to show both anti-inflammatory and immune-stimulating effects. However, the anticancerogenic effect of LBP is also thought to occur with the immune-stimulatory effect.[52] In our study, the induction of AP with cerulein was observed to cause an increase in levels of inflammation mediators such as IL-6, IL-1 resulting in corresponding pancreatic inflammation. According to our findings, IL-1 and IL-6 levels were increased in the AP group compared to the control group, and it was observed that these increased cytokine levels decreased significantly with LB administration. Similar to our findings, in a study conducted by Xiong et al., in the AP model with cerulein in mice, the delivery of LB polysaccharides resulted in a decrease in the level of IL-6 and TNfA, which has increased due to AP.[34] These data show that the LB plant has an anti-inflammatory effect. In the study of Qi et al., the changes observed in IL-1 and IL-6 levels with the administration of LBP against AKI are consistent with the findings of our study.[17]{Table 1}

In addition to the findings we obtained in our study, we examined the kidney tissues histopathologically. In our findings, dilation in the bowman ranges of the kidneys and consequent pressure increase point to intercellular fluid increase and picnotic and heterochromatic nucleus structure in proximal and distal tubule epithelial cells. These findings, which we observed in kidney tissue sections, prove that kidney tissue damage was formed in the AP group. Tissue damage occurring outside of the pancreas is usually a complication that occurs with acute necrotizing pancreatitis, and in line with histological data, we can say that the model developed in our experimental animals is compatible with necrosis of pancreatitis. The underlying pathological findings in the kidney tissue are the congestion and collapse caused by renal circulatory disorder and the oxidative stress triggered by the ischemia shaped accordingly. In many studies in the literature, findings in AKI associated with AP support the findings in our study.[53],[54],[55]

We examined antioxidant parameters such as SOD, GPx, CAT, MDA, and 8-OHdG to reveal kidney damage and oxidative stress. In our study, there was a significant reduction in kidney SOD and GPx activities compared with the control group of the AP model, while there was an increase in CAT activity and MDA level. With LB administration, there was an increase in kidney SOD and GPx activities and a decrease in MDA level. These results show that kidney damage and oxidative stress due to AP can be cured by LB. It is thought that this effect of LB is due to the anti-inflammatory and antioxidant-effective components it contains. The changes observed in SOD, GPx and MDA parameters through the use of the LB plant in many studies support the findings we have made in our study. However, CAT showed an increase unlike other antioxidant enzymes SOD and GPx. CAT and GPx are two antioxidant enzymes responsible for the detoxification of hydrogen peroxide and other organic peroxides. During the dismutation of superoxide radicals, which are intensely produced during oxidative stress, a significant amount of hydrogen peroxide is formed by the SOD enzyme. GPx provides the first line of defense in the detoxification of accumulated peroxides and therefore GPX activity begins to decrease faster than the CAT enzyme. In fact, the presence of peroxide at low concentrations can stimulate CAT enzyme production and cause high activity to be measured.[26],[35],[51],[52],[56] The changes observed in SOD activity and MDA levels by Xie et al., given different doses of LBP (200, 400, and 600 mg/kg b. wt) against kidney damage caused by lead acetate in mice support the findings of our study.[57] In many studies, the use of LB has shown positive results in diseases that develop due to oxidative stress in different organs.[58],[59] In these studies, the observed changes in antioxidant parameters (SOD, GPx, and MDA) are in agreement with the data we obtained in our study. These results show us that the use of LB in many organ damage with its antioxidative effects is promising in obtaining positive results.

On the other hand, the increase of free radicals in the cell causes significant damage to DNA. 8-OHdG is considered to be the most important indicator of DNA damage.[60],[61],[62],[63] The increase in the amount of 8-OHdG probably occurs as a result of oxidative interference of mitochondrial and nuclear DNA by free radicals.[64] It has been shown that LBP has protective effects against DNA damage in the pancreas in diabetic rats.[65] In the findings of our study, no significant difference was observed in tissue 8-OHdG level depending on the development of AP. This may be due to the more conserved localization of nuclear and mitochondrial DNA in the cell. However, administration of LB caused a decrease in 8-OHdG levels. This result suggests that LB extract can reverse the hydroxylations that occur in DNA. There is a need for extensive studies at the molecular level on this subject.

 Conclusion



Pancreatic tissue is often focused on in AP, and possible damage and loss of function in other organs are not taken into account sufficiently. However, damage to other organs, especially kidney, is as important as pancreatic damage caused by AP. LB extract can be considered as a protective agent against kidney damage and oxidative stress caused by AP. In addition, it can reduce local and systemic effects by limiting the severity of fire, which is the most important factor determining the prognosis of the disease, with its anti-inflammatory effects. Although the protective activity of LB was demonstrated in this study, the bioactive molecules responsible for these effects should be separated and their share in the activity should be determined in future studies.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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