ETM Experimental and Therapeutic Medicine 1792-0981 1792-1015 D.A. Spandidos 10.3892/etm.2018.6683 ETM-0-0-6683 Articles Protective effect of dexpanthenol against cisplatin-induced hepatotoxicity BilgicYilmaz 1 AkbulutSami 2 AksungurZeynep 3 ErdemliMehmet Erman 4 OzhanOnural 5 ParlakpinarHakan 5 VardiNigar 6 TurkozYusuf 3 Department of Gastroenterology, Inonu University Faculty of Medicine, Malatya 44280, Turkey Department of Surgery and Liver Transplant Institute, Inonu University Faculty of Medicine, Malatya 44280, Turkey Department of Biochemistry, Inonu University Faculty of Medicine, Malatya 44280, Turkey Department of Biochemistry, Nigde Omer Halisdemir University Faculty of Medicine, Nigde 51240, Turkey Department of Pharmacology, Inonu University Faculty of Medicine, Malatya 44280, Turkey Department of Embryology and Histology, Inonu University Faculty of Medicine, Malatya 44280, Turkey Correspondence to: Dr Sami Akbulut, Department of Surgery and Liver Transplant Institute, Inonu University Faculty of Medicine, Elazig Yolu 10 Km, Malatya 44280, Turkey, E-mail: akbulutsami@gmail.com 11 2018 03 09 2018 16 5 4049 4057 05032018 13072018 Copyright: © Bilgic et al. 2018 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

The aim of the present study was to investigate the protective effect of dexpanthenol (Dexp) against cisplatin (Cis)-induced hepatotoxicity. Thirty-two Sprague Dawley rats were divided into four groups: Control group (n=8), Dexp group (n=8, 500 mg/kg/ip/daily single dose/3 days Dexp), Cis group (n=8, 7 mg/kg/ip/single dose Cis) and Cis+Dexp group (n=8, 500 mg/kg/ip/daily single dose/3 days Dexp +7 mg/kg/ip/single dose Cis). MDA, CAT, GSH, GSH-Px, TOS, TAS, OSI, Total Nitrit, IL-1β, IL-6 and TNF-α levels were analyzed in liver tissue samples. After paraffinization of liver tissue samples, histopathological (congestion, loss of glycogen, number of Kupffer cells) and immunohistochemical (caspase-3 expression) parameters were assessed on the paraffinized liver sections. GSH, TAS, TOS, OSI, Tot Nit, L-Arginine, ADMA and SDMA levels were measured in the serum samples. Statistically significant differences were found between the groups in terms of all liver tissue biochemical parameters, with the exception of IL-1β and TNF-α levels. GSH, CAT, GSH-Px, TAS and Tot Nit levels were significantly higher in the Cis+Dexp group compared to the Cis group, whereas MDA, TOS, OSI and IL-6 levels were higher in the Cis group. Similarly, serum GSH, TAS, Tot Nit levels were higher in the Cis+Dexp group whereas TOS, L-Arginine, ADMA and SDMA levels were higher in Cis group. There were statistically significant differences between Control and Cis groups in terms of congestion increase, increase of glycogen loss, increase of Kupffer cell number and increase of caspase-3 expression (P<0.001). There was a statistically significant difference between the Cis and the Cis+Dexp groups in terms of histopathologic parameters, with the exception of congestion (P<0.001). To conclude, histopathological, immunohistochemical, and biochemical results of this study demonstrated that Dexp has a protective effect against Cis-induced hepatotoxicity.

 cisplatin hepatotoxicity dexpanthenol antioxidant potential Introduction

Cisplatin (Cis), whose antineoplastic efficacy was discovered in 1960s, is a platinum-derivative antineoplastic agent used to treat a variety of solid organ tumors such as testis, ovaries, urinary bladder, head and neck, brain, and lungs (1–5). Despite its potent antineoplastic efficacy, Cis's toxic side effects during treatment such as nephrotoxicity, neurotoxicity, ototoxicity, myelosuppression, hepatotoxicity limits its clinical use (1–5). Studies investigating the relationship between Cis dose and toxic side effects have mostly suggested a correlation between Cis's cumulative dose and toxic side effects. This is particularly prominent for the liver and hematopoietic system (1–6). However, it has been shown that hepatotoxicity may also develop after a single dose or low repeated doses (1).

Although there is no consensus as to the mechanism of Cis-induced hepatotoxicity, the two most widely recognized views are the shift of the antioxidant balance towards oxidative stress and acceleration of apoptosis (1,3,7). Cells exposed to oxidative stress eliminate reactive oxygen species (superoxide, hydroxyl, hydrogen peroxide) and reactive nitrogen species [nitric oxide (NO), nitrogen dioxide, and peroxynitrite] by using endogenous enzymatic antioxidants (SOD, GSH-Px, CAT, GSR), endogenous nonenzymatic antioxidants (GSH, thioredoxin, melatonin), and exogenous antioxidants (ascorbic acid, α-tocopherol, retinol, α-carotene, β-carotene, lycopene, cryptoxanthin, zinc, copper, manganese, iron, selenium, flavonoids, phenols, phenolic acid, lignins, tannins). Experimental studies using many antioxidants, free radical scavengers, and natural herbal compounds have been conducted to prevent Cis's side effects without limiting its antineoplastic efficacy. Other than the above-mentioned antioxidants, antioxidant substances including apocynin, thymoquinone, naringenin-oxime, curcumin, silymarin, resveratrol, gingko, phosphomycine, sodium thiosulfate, n-acetyl-cysteine, methionine, taurine, and dexpanthenol (Dexp) have been most heavily studied in the literature.

Dexp is a pantothenic acid (PA) analogue oxidized to PA in peripheral tissues. PA and its derivatives are known to increase reduced glutathione (GSH) and coenzyme A (CoA) levels and augment ATP synthesis. All of these functions play an important role for cellular protection against oxidative stress and inflammatory response (1,8–13). Therefore, studies on antineoplastic agents exerting toxic side effects through oxidative stress mechanism have traditionally used Dexp. In this experimental study, we aimed to investigate the protective effects of Dexp against Cis-induced hepatotoxicity.

 Materials and methods <sec> <title>Rat selection

Thirty-two Sprague Dawley rats aged 11 to 12 weeks weighing 230 to 300 grams were obtained from Experimental Animal Research Center of Inonu University, Malatya, Turkey. The rats were fed on standard rat feed and provided water ad libitum. They were kept under laboratory conditions (21±2°C, % 60±5 moisture and 12:12 h light/dark cycle). All procedures applied to the rats complied with the National Health Institute's Guidelines for Animal Research. The experimental groups were formed by the simple randomization technique.

 Institutional approvals

This study was approved by Inonu University Faculty of Medicine Animal Research Ethics Committee (2016/A-36). It was funded by Inonu University Scientific Research Project Coordination Unit (Project no. 2016/179).

 Experimental design

Thirty-two rats were divided into four groups each containing an equal number of rats (n=8). The study groups were defined as follows: The rats of the control group were not administered anything else than standard rat feed and water. The rats in the Dexp group were administered a single dose intraperitoneal Dexp at a dose of 500 mg/kg for 3 days (Bepanthene 500 mg vials, Bayer Corp, Istanbul, Turkey) (12). The dosage range at which Dexp exerts its cytoprotective effect has been shown by the previous studies. Hence, we calculated the effective Dexp dose on the basis of the literature studies (4,8,12). Although the duration of Dexp use ranged between 1 and 12 days in the previous experimental studies about the Dexp's cytoprotective effect, we limited that duration to 3 days (12). The rats in the Cis group were administered a single dose of Cis at a dose of 7 mg/kg only on the first day of the study (Cis 50 mg vials; Kocak Pharma, İstanbul, Turkey) (2,7). The dosage range at which Cis exerts its cytotoxic (hepatotoxic) effects has been shown by the previous experimental studies (2,7). The rats in the Cis+Dexp group were administered intraperitoneal Dexp at a dose of 500 mg/kg for three days. One hour after the first Dexp dose a single intraperitoneal dose of 7 mg/kg Cis was administered. All rats were sacrificed by ketamine hydrochloride (Ketalar 500 mg vials; Pfizer Inc., NY, USA) overdose at the end of the fourth day of the follow-up period. Immediately before the scarification procedure blood samples were collected from the inferior vena cava for biochemical analysis. Hepatectomy was carried out after blood collection, and part of the hepatectomy material was fixated with formalin for histopathological examination and the remaining tissues were stored at −70°C for biochemical analysis.

 Biochemical analysis

At the end of study period, the animals were anesthetized and blood samples were withdrawn into evacuated tubes by vena cava inferior puncture. Then the rats were sacrificed and taken their livers. The liver samples were frozen at −70°C until assayed. The liver samples were homogenized in cold phosphate buffer (20 mmol; pH 7.4; containing protease inhibitor cocktail, BioShop Canada Inc., Burlington, ON, Canada) with a homogenizer (IKA ultra turrax T 25 basic) at 16,000 rpm for 3 min at +4°C. The homogenats were centrifuged at 10,000 × g for 20 min at +4°C and the obtained supernatants were used to measure the levels of MDA, GSH, GSH-Px, CAT, total nitrite, IL-1β, IL-6, TNF-α, TAS, and TOS. The blood samples taken from rats were centrifuged at 2,000 × g for 10 min at +4°C and the obtained serum samples were used to measure the levels of GSH, TAS, TOS, total nitrite, l-arginine, ADMA, and SDMA. The serum samples were frozen at −70°C until assayed.

 Malondialdehyde (MDA) assay

MDA, referred to as thiobarbituric acid reactive substances (TBARS), was measured with thiobarbituric acid at 535 and 520 nm in spectrophotometer using a microplate reader (Synergy H1; BioTek Instruments, Inc.) as previously described (14). Results were reported as nmol/g wet tissue for tissue.

 Reduced GSH assay

GSH concentrations in the homogenate and serum samples were measured according to the spectrophotometric Ellman's method (15). Results were reported as nmol/g wet tissue for tissue and micromole/l for serum.

 Catalase (CAT) activity assay

CAT activity was determined according to the method of Aebi (16) by monitoring the initial rate of disappearance of hydrogen peroxide (initial concentration 10 mM) at 240 nm in a spectrophotometer (microplate reader; Synergy H1). Results were reported as constant rate per gram protein (K/g protein).

 GSH-peroxidase (Px) activity assay

GSH-Px activity was measured according to Paglia and Valentine (17) by monitoring the oxidation of reduced nicotinamide adenine dinucleotide phosphate (NADPH) at 340 nm. Results were reported as units per gram protein (U/g protein).

 Protein assay

Protein concentrations of the supernatant samples were measured the method of Lowry et al (18).

 NO assay

NO level of the supernatant and serum samples was measured as total nitrite with the spectrophotometric Griess reaction. Because, it was showed that plasma nitrite/nitrate is an index of endogenous NO production (19,20). The procedure was partly adapted from the method described by Ozbek et al (21) Results were reported as nanomole/g wet tissue for tissue and micromole/liter for serum.

 Measurement of the supernatant and serum ADMA, SDMA, and L-arginine levels

The supernatant and serum ADMA, SDMA, and L-arginine concentrations were measured with high performance liquid chromatography using commercially available kits (Eureka Laboratory Division s.r.l., Chiaravalle, Italy). The results were expressed as micromole/liter.

 Measurement of the supernatant and serum total antioxidant status (TAS) and total oxidant status (TOS) levels

The supernatant and serum TAS and TOS concentrations were measured with spectrophotometer (microplate reader; Synergy H1) using commercially available kits (Rel Assay Diagnostics, Gaziantep, Turkey). The results were expressed as millimole Trolox Eqv/liter for TAS and micromole H2O2 Eqv/liter for TOS.

 Measurement of the supernatant IL-1β, IL-6, TNF-α levels

The supernatant IL-1β, IL-6, TNF-α levels was measured spectrophotometrically using Elabscience Raybiotech commercial kits (microplate reader; Synergy H1).

 Oxidative stress index (OSI)

The ratio of TOS to TAS was accepted as OSI. The OSI value was calculated according to the following formula: OSI (arbitrary unit)=TOS (micromole H2O2 Eqv/liter)/TAS (millimole Trolox Eqv/liter) (22).

 Histopathological analysis

Liver tissue was fixed in 10% formalin and was embedded in paraffin. Tissue sections were cut at 4 µm, mounted on slides, stained with hematoxylin and eosin (H&E) for general liver structure, Periodic Acid Schiff (PAS) to demonstrate the glycogen deposition in hepatocytes and Kupffer cells. The liver damage was semi quantitatively assessed as follows; sinusoidal congestion, and loss of the glycogen deposition in hepatocytes. The sinusoidal congestion, and glycogen loss were scored between 0–3; 0 was defined as normal liver, 1 was defined as liver damage involving ≤25% of liver, 2 was defined as liver damage involving 25–50% of liver and 3 was defined as liver damage involving ≥50% of liver. For each criterion, ten fields were examined in X20 objective magnification. In addition, Kupffer cells were counted manually on digital images Leica Q Win analysis system using point counting. For each animal, three sections were used. In each section, 10 fields were randomly chosen at 40X, totaling 30 fields per animal.

 Immunohistochemical analysis

After deparaffinization and rehydration procedures, sections were placed in antigen retrieval solution (citrate buffer, pH 6.0) and boiled in a pressure cooker for 20 min and cooled to room temperature for 20 min. Then the sections were washed with phosphate-buffered saline (PBS). After washing the sections, 3% hydrogen peroxide solution was applied to block endogenous peroxide for 15 min at room temperature and washed with PBS. Then protein block was applied to the sections. The sections were incubated with caspase-3 primary antibody (rabbit polyclonal; Thermo Fisher Scientific, Inc.) for 60 min, then were rinsed in PBS and incubated with biotinylated goat anti polyvalent for 20 min and streptavidin Px for 20 min at room temperature. Staining was completed with chromogen+substrate for 10 min, and slides were counter stained with Mayer's hematoxylin for 1 min, rinsed in tap water, and dehydrated. Caspase-3 positive cells stained as brown color. The expression of caspase-3 was assessed as follows: 0, no expression; 1, minimal expression (involving ≤25% of liver); 2, moderate expression (involving 25–50% of liver) and 3, severe expression (involving ≥50% of liver). For this analysis ten fields were examined in objective magnification, ×20. All sections were evaluated using a Leica DFC280 light microscope and a Leica Q Win Image Analysis system (Leica Micros Imaging Solutions Ltd., Cambridge, UK).

 Statistical analysis

The results of the histologic examination were compared using SPSS software (Chicago, IL, USA) version 17 for Microsoft Windows. Mann-Whitney U (Bonferroni) test was used for comparison between groups. The results of the biochemical analysis were compared using SPSS software (SPSS, Chicago, IL, USA) version 22.0 for Microsoft Windows. Kruskal-Wallis test was used for comparison between groups. When significant differences were determined in Kruskal-Wallis test, pairwise comparisons were carry out using Conover's test. The results are expressed as the med (min-max). P<0.05 was considered to indicate a statistically significant difference.

 Results Biochemical results Tissue biochemical results

As all biochemical parameters measured in the liver tissues showed a nonparametric distribution, Kruskal-Wallis test was used for inter-group comparisons. There were significant inter-group differences with respect to MDA (P=0.001), GSH (P=0.001), CAT (P=0.001), GHS-Px (P=0.001), Total Nitrite (P=0.001), TAS (P=0.001), TOS (P=0.001), OSI (P=0.001) and IL-6 (P=0.017) levels whereas tissue L-1β (P<0.081) and TNF-α (P<0.322) levels were comparable. For groups that were found to have statistical differences, Conover test was applied to find out the different pairs. Significant differences were found between all groups with respect to tissue MDA, CAT and Total Nitrite levels. Whereas there were no significant differences between the Control and Dexp groups in terms of tissue GHS-Px, TOS and OSI, the Cis and Cis+Dexp groups showed significant differences from the other groups. Whereas the Control and Cis groups did not show any significant differences for tissue GSH level, Dexp and Cis+Dexp groups were significantly different from the other groups. Although no significant differences existed between the control and Cis+Dexp groups with regard to tissue TAS level, the Dexp and Cis groups were significantly different from the other groups. A significant difference existed between tissue IL-6 levels of the Dexp and Cis groups. Table I summarizes the results of the tissue biochemical parameters.

 Serum biochemistry results

As all biochemical parameters obtained from the serum samples showed a nonparametric distribution, inter-group comparisons were carried out using the Kruskal-Wallis test. The groups had significant differences with regard to serum GSH (P=0.014), TAS (P=0.003), OSI (P=0.004), Total Nitrite (P=0.003), L-Arginine (P=0.003), ADMA (P=0.026) and SDMA (P=0.022) levels whereas serum TOS (P<0.058) levels were similar. Serum biochemistry results were presented on Table II.

 Histopathological results Hematoxylin and eosin

Liver tissue of the Control and Dexp groups showed entirely normal histological appearance but minimal changes. Sinusoidal congestion was the most prominent alteration in the Cis group. Furthermore, hepatocytes with eosinophilic cytoplasm and pyknotic nuclei were detected in some sections. The Cis+Dexp group showed similarities with the Cis group in terms of histological changes. Table III shows congestion scores of the study groups.

 PAS

In the Control and Dexp groups, glycogen and Kupffer cells (Fig. 1a and b) in the hepatocyte cytoplasm were stained with pink and purple stain. As compared with the controls, the Cis group showed a reduced amount of glycogen accumulation in hepatocytes (P<0.001). Additionally, the Cis group, as compared to the Control and Dexp groups, had a significantly increased number of Kupffer cells (Fig. 1c) (P<0.001). In the Dexp group, glycogen loss in hepatocytes was significantly reduced (Fig. 2d) (P<0.001). Furthermore, Cis+Dexp group showed a significant reduction in the number of Kupffer cells as compared to the Cis group. (Fig. 1d) (P<0.001).

 Immunohistochemical results

The control and Dexp groups had no caspase-3 expression in the tissue sections except for a few hepatocytes (Fig. 2a and b). On the other hand, there was a significant increase in the caspase-3 expression in the Cis group (P<0.001) (Fig. 2c). That group also demonstrated an increased caspase-3 staining intensity. However, Cis+Dexp group had a significant decrease in the caspase-3 expression (P<0.001) (Fig. 2d). Table III shows the immunohistochemical staining scores of the study groups.

 Discussion

Although several experimental studies have reported hepatotoxicity occurring with high doses of Cis, some others have indicated that the former may occur even with a single dose or low prolonged doses use of Cis (1,6). As Cis is a small molecule, it easily passes through the cell membrane to reach cell nucleus and alter DNA structure (5). Although the pathophysiological mechanism of Cis-induced hepatotoxicity has yet to be fully understood, recent studies have shown that a considerable proportion of its toxic side effects originate from oxidative stress and apoptosis (1,5). Studies on Cis toxicity showing reduced hepatic GSH levels and increased hepatic MDA levels have corroborated the notion that Cis toxicity is linked with oxidative stress of hepatocytes (5). Therefore, experimental studies have so far employed many antioxidants, free radical scavengers, and natural herbal extracts considered to have protective properties against Cis-associated cytotoxicity.

Oxidative stress may be defined as overproduction of reactive oxygen species and/or failure of antioxidant mechanisms (3). Reactive oxygen species produced by normal metabolism are eliminated in the liver by certain reactions in which enzymes such as superoxide dismutase, catalase, GSH Pxs, and peroxiredoxin are involved (5,23). When the liver is exposed to oxidative stress as in Cis-induced hepatotoxicity, liver cells encounter large quantities of reactive oxygen species that overwhelm their detoxification capacity. Reactive oxygen species then cause hepatocyte injury by injuring DNA (increased cell death, reduced proliferation), protein oxidation (growth factor inhibition, reduced enzymatic functions), lipid peroxidation (inflammation, radical formation) and direct action on signal pathways (transcription factor activation, reduced angiogenesis, reduced NO level) (5,23).

In the present experimental study model, we aimed to investigate if Dexp would exert any cytoprotective and antioxidant effect on Cis-induced hepatotoxicity. According to the most recent literature data, an important percentage of Cis related side effects occur through oxidative stress pathways. Based on this information, we studied several oxidative stress parameters in liver tissue and blood samples. The levels of tissue antioxidant parameters (GSH, CAT, GSH-Px, TAS) were significantly greater in the Cis+ Dexp group compared to the Cis group. In contrast, the levels of oxidative stress products (MDA, TOS, OSI) were significantly greater in the Cis group than the Cis+Dexp group. Similarly, serum GSH and TAS levels were greater in the Cis+Dexp group whereas serum TOS and L-Arginine levels were greater in the Cis group. These results suggest that Dexp minimizes Cis's hepatotoxic effect by intensifying antioxidant mechanisms.

ADMA and SDMA are toxic non-proteinogenic amino acids formed by post-translational modification. These toxic dimethylarginines were first detected in human urine in 1970. Both of them suppress NO production by inhibiting the Nitric Oxide Synthase (NOS) enzyme. Clinical and experimental studies have shown that ADMA and SDMA play a role in the pathophysiological mechanism of endothelial dysfunction, atherosclerosis, oxidative stress, inflammation, and apoptosis (24). ADMA disintegrates NOS into its isoenzymes to produce superoxide radicals that are involved in oxidative stress (24). SDMA, unlike ADMA, induces pathways involved in the production of free oxygen species and has therefore proinflammatory and prooxidant properties (24). In our study the Cis+Dexp group had significantly lower blood ADMA, SDMA, and L-Arginine levels than the Cis group. In contrast, the Cis+Dexp group had a significantly higher total nitrite levels than the Cis group. These results suggest that since Dexp reduced ADMA and SDMA levels, the NOS enzyme was not inhibited and Arginine was converted into NO molecule, which reduced blood arginine level in the Cis+Dexp group.

Another important point to stress is the mechanism of the alterations of blood and tissue NO levels. A general consensus exists that NO behaves differently in physiological and pathological conditions. It is known that many hepatotoxic drugs and chemical substances increase hepatic NO production by inhibiting iNOS enzyme and are converted to peroxynitrite by reacting with NO's superoxide anion, causing hepatic injury via nitrous active stress (25). In this regard, our results do not overlap with the literature data. This is because both tissue and blood total nitrite levels were significantly higher in the Dexp and Cis+Dexp groups compared to the Cis group. Moreover, total nitrite levels were even higher in the Cis group than the control group. That is, in contrast with the literature data, the findings of the present study indicate that antioxidant agents increased NO levels rather than reducing them. To our opinion, this finding may be related to a reduction of ADMA and SDMA levels by Dexp, as we pointed above. Nevertheless, in any case, this point needs to be confirmed by other studies.

Cytokines playing a role in both proinflammatory and anti-inflammatory stages of inflammation are the major molecules that have been investigated by inflammation models (11,26). As the liver hosts receptors belonging to many different varieties of cytokines, it has been widely studied in inflammation models. Reactive oxygen species produced during oxidative stress may further augment Cis's cytotoxic effects in the liver by increasing nuclear kappa factor B expression and release of proinflammatory cytokines (particularly IL-1β, TNF-α, and IL-6) (2,26). We aimed to investigate how proinflammatory cytokines behave in Cis-induced hepatotoxicity and how Dexp affects their tissue levels. Accordingly, although tissue IL-6 and TNF-α levels were higher in the Cis group compared to the Cis+Dexp group, this difference did not reach statistical significance. However, these findings show parallelism with the literature data with regard to their mathematical results (11). In contrast, tissue IL-1β level was found lower in the Cis group than the Cis+Dexp group. This finding about IL-1β contradicts with the literature data. To our opinion, this contradiction should be corroborated or refuted by future studies.

We discussed above that an important proportion of Cis's side effects occur through oxidative stress pathways. Another mechanism responsible for the genesis of toxic side effects is apoptosis (1). Increased intracellular levels of reactive oxygen species result in DNA injury in the cell nucleus, and when that injury could not be repaired, both proliferation is limited and apoptosis is augmented (23). Many experimental ischemia reperfusion injury and hepatotoxicity models studied the relationship between antioxidant or free radical scavenging agents and apoptosis by both immunohistochemical staining techniques (active caspase-3, split PARP, TUNEL) and tissue/blood biochemical parameters (IL-6, TNF-α, caspase-3 activity, DNA fragmentation) (1,2). We studied immunohistochemically caspase-3 expression to assess apoptosis. In the Cis+Dexp group caspase-3 expression was significantly lower than in the Cis group. The overall findings of our study suggest that Dexp reduced apoptosis both by directly eliminating reactive oxygen species that accelerate apoptosis and by reducing the level of the ADMA molecule that induces apoptosis (27).

We would like to mention some points that limited us in this experimental study. The first limiting factor was that we did not studied serum and tissue parameters indicative of nephrotoxicity although the latter is the main most serious side effect of Cis (28). In the present study we had the opportunity to show both the nephrotoxic effects of Cis and the nephroprotective effects of Dexp (29). However, as the study designs solely focused on the liver, renal effects were unfortunately ignored. The second limiting factor was the absence of the determination of AST, ALT, ALP, and bilirubin levels, which are directly indicative of hepatic injury, although many tissue and serum parameters indicative of oxidative stress, antioxidant response, and apoptosis. The previous experimental studies examining the hepatotoxic effects of Cis showed marked alterations in ALT, AST, and ALP levels (28).

As far as we know, this is the first study in the literature that specifically studied the protective effect of Dexp against Cis-induced hepatotoxicity. Hence, it is clear that the findings of the present study need to be supported by other studies designed with the same model. In conclusion, in this experimental study model we demonstrated that Dexp exerted a hepatoprotective, antioxidant, and antiapoptotic action; in other words, it minimized Cis-induced hepatotoxicity.

 Acknowledgements

Not applicable.

 Funding

The present study was supported by the Inonu University Scientific Research Project Coordination Unit (grant no. 2016/179).

 Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

 Authors' contributions

YB, SA, HP and YT designed and directed the experiments. YB, SA, OO and YT performed the experiments. MEE, ZA and YT performed biochemical analysis. NV performed histopathological analysis. SA performed the statistical analysis. SA wrote the manuscript. YB, SA, HP and YT reviewed and edited the manuscript. All authors read and approved the final manuscript.

 Ethics approval and consent to participate

The animal use protocol was reviewed and approved by the Inonu University Faculty of Medicine Animal Research Ethics Committee (2016/A-36). All animals received humane care in compliance with the Guide for the Care and Use of Laboratory Animals published by the National Institutes of Health.

 Patient consent for publication

Not applicable.

 Competing interests

The authors declare that they have no competing interests.

 References CaginYFAtayanYSahinNParlakpinarHPolatAVardiNTaglukMETanbekKYildizABeneficial effects of dexpanthenol on mesenteric ischemia and reperfusion injury in experimental rat modelFree Radic Res50354365201610.3109/10715762.2015.112683426631422 CureMCCureEKalkanYKırbaşATümkayaLYılmazATürkyılmazAKŞehitoğluİYüceSInfliximab modulates cisplatin-induced hepatotoxicity in ratsBalkan Med J33504511201610.5152/balkanmedj.2016.15057627761277 KaraleSKamathJVEffect of daidzein on cisplatin-induced hematotoxicity and hepatotoxicity in experimental ratsIndian J Pharmacol494954201728458422 TopluYSapmazEParlakpinarHKellesMKalciogluMTTanbekKKizilayAThe effect of dexpanthenol on ototoxicity induced by cisplatinClin Exp Otorhinolaryngol91420201610.21053/ceo.2016.9.1.1426976021 Al-MalkiALSayedAAThymoquinone attenuates cisplatin-induced hepatotoxicity via nuclear factor kappa-βBMC Complement Altern Med14282201410.1186/1472-6882-14-28225088145 AstolfiLGhiselliSGuaranVChiccaMSimoniEOlivettoELelliGMartiniACorrelation of adverse effects of cisplatin administration in patients affected by solid tumours: A retrospective evaluationOncol Rep2912851292201310.3892/or.2013.227923404427 KoyuncuIKocyigitAGonelAArslanEDurgunMThe protective effect of naringenin-oxime on cisplatin-induced toxicity in ratsBiochem Res Int20179478958201710.1155/2017/947895828932603 ErmisHParlakpinarHGulbasGVardiNPolatACetinAKilicTAytemurZAProtective effect of dexpanthenol on bleomycin-induced pulmonary fibrosis in ratsNaunyn Schmiedebergs Arch Pharmacol38611031110201310.1007/s00210-013-0908-623995256 KaradagAOzdemirRKurtAParlakpinarHPolatAVardiNTaslidereEKaramanAProtective effects of dexpanthenol in an experimental model of necrotizing enterocolitisJ Pediatr Surg5011191124201510.1016/j.jpedsurg.2014.10.05325783305 KarapinarSoylu OPinarNOzgürTÖzcanOBayraktarHSKurtRKNuralOThe protective role of dexpanthenol on the endometrial implants in an experimentally induced rat endometriosis modelReprod Sci24285290201710.1177/193371911665368227313118 Li-MeiWJieTShan-HeWDong-MeiMPeng-JiuYAnti-inflammatory and Anti-oxidative Effects of Dexpanthenol on Lipopolysaccharide Induced Acute Lung Injury in MiceInflammation3917571763201610.1007/s10753-016-0410-727469104 SenHDenizSYedekciAEInangilGMuftuogluTHaholuAOzkanSEffects of dexpanthenol and N-acetylcysteine pretreatment in rats before renal ischemia/reperfusion injuryRen Fail3615701574201410.3109/0886022X.2014.94976825156619 UysalHBDagliBYilmazMKahyaogluFGokcimenAOmurluIKDemirciBProtective effects of dexpanthenol against acetaminophen-induced hepatorenal damageBiomed Res287407492017 MiharaMUchiyamaMDetermination of malonaldehyde precursor in tissues by thiobarbituric acid testAnal Biochem86271278197810.1016/0003-2697(78)90342-1655387 EllmanGLTissue sulphydryl groupsArch Biochem Biophys827077195910.1016/0003-9861(59)90090-613650640 AebiHBergmeterHUMethods in enzymatic analysis, Weinheim, Verlag Chemie 312821982 PagliaDValentineWNStudies on the quantitative and qualitative charecterization of erythrocyte glutathione peroxidaseJ Lab Clin Med7015816919676066618 LowryOHRosenbroughNJFarrALRandallRJProtein measurement with the folin phenol reagentJ Biol Chem193265275195114907713 JungerstenLEdlundAPeterssonASWennmalmAPlasma nitrate as an index of nitric oxide formation in man: Analyses of kinetics and confounding factorsClin Physiol16369379199610.1111/j.1475-097X.1996.tb00726.x8842573 ZeballosGABernsteinRDThompsonCIForfiaPRSeyediNShenWKaminiskiPMWolinMSHintzeTHPharmacodynamics of plasma nitrate/nitrite as an indication of nitric oxide formation in conscious dogsCirculation9129822988199510.1161/01.CIR.91.12.29827796509 OzbekETurkozYGokdenizRDavarciMOzugurluFIncreased nitric oxide production in the spermatic vein of patients with varicoceleEur Urol37172175200010.1159/00002013510705195 ErelOA new automated colorimetric method for measuring total oxidant statusClin Biochem3811031111200510.1016/j.clinbiochem.2005.08.00816214125 AutenRLDavisJMOxygen toxicity and reactive oxygen species: the devil is in the detailsPediatr Res66121127200910.1203/PDR.0b013e3181a9eafb19390491 TainYLHsuCNToxic dimethylarginines: Asymmetric Dimethylarginine (ADMA) and Symmetric Dimethylarginine (SDMA)Toxins (Basel)9E92201710.3390/toxins903009228272322 SinghHSidhuSChopraKKhanMUThe novel role of β-aescin in attenuating CCl4-induced hepatotoxicity in ratsPharm Biol55749757201710.1080/13880209.2016.127502328064552 KandilYIMaraqaADOriquatGAShraidehZAResveratrol pretreatment reduces circulating inflammatory interleukins in CCl4-induced hepatotoxicity ratsBulletin Faculty Pharm Cairo Univ55319323201710.1016/j.bfopcu.2017.09.005 YeSZhouX2LinJChenPAsymmetric dimethylarginine induced apoptosis and dysfunction of endothelial progenitor cells: Role of endoplasmic reticulum stress pathwayBiomed Res Int20176395601201710.1155/2017/639560128589144 PezeshkiZKhosraviANekueiMKhoshnoodSZandiEEslamianMTalebiAEmamiSNNematbakhshMTime course of cisplatin-induced nephrotoxicity and hepatotoxicityJ Nephropathol6163167201710.15171/jnp.2017.2828975096 DoganEEErkocREkinciIHamdardJDonerBCikrikciogluMAKaratoprakCCobanGOzerOFKazanciogluRProtective effect of dexpanthenol against nephrotoxic effect of amikacin: An experimental studyBiomed Pharmacother8914091414201710.1016/j.biopha.2017.03.01928320109

(a) Control and (b) Dexp groups; PAS positive reaction show a magenta staining in which Kupffer cells were present in the lumen or near the wall of sinusoid (arrows). (c) Cis group; an increased number of Kupffer cells (arrows) were indicated. (d) Cis+ Dexp group; a decreased number of Kupffer cells (arrows) were indicated (magnification, ×40). Cis, cisplatin; Dexp, dexpanthenol.

(a) Control and (b) Dexp groups; caspase-3 expression was observed as negative. (c) Cis group; caspase-3 (+) cells were distinguished by brown cytoplasm (stars). (d) Cis+Dexp group; hepatocytes were not stained with caspase-3 (magnification, ×20). Cis, cisplatin; Dexp, dexpanthenol.

Comparison of biochemical parameters measured in liver tissue.

Parameters Group Median Minimum Maximum P
MDA (nmol/gr wet tissue) Controla 659.9 592.9 854.2 0.001
Dexpb 512.5 197.6 629.8
Cisc 1334.9 783.9 1999.9
Cis+Dexpd 904.5 673.3 1139
GSH (nmol/gr wet tissue) Controla 2035.2 1781.9 2140.9 0.001
Dexpb 2769.1 2602.4 3198.6
Cisc 1612.1 1346.1 1865.3
Cis+Dexpa 2019.1 1852.5 2506.3
CAT (K/g protein) Controla 24.1 20.1 30.3 0.001
Dexpb 51.4 48.4 57.2
Cisc 13.2 12.3 15.9
Cis+Dexpd 30.7 25.3 39.2
GSH-Px (U/g protein) Controla 101.1 90.0 118.3 0.001
Dexpa 107 95.9 125.9
Cisb 59.8 45.4 95.47
Cis+Dexpa 89.2 71.8 108.1
Tot Nit (nmol/gr wet tissue) Controla 275.4 266.4 298.8 0.001
Dexpb 349.2 288 381.6
Cisc 248.4 216 273.6
Cis+Dexpd 298.8 266.4 324
TAS (mmol Trolox Eqv/l) Controla 2.2 2.1 2.54 0.001
Dexpb 2.5 2.4 2.6
Cisc 1.8 1.7 1.85
Cis+Dexpa 2.1 1.9 2.31
TOS (µmol H2O2 Eqv/l) Controla 26.2 19.5 33.8 0.001
Dexpa 24.1 20.1 31.8
Cisb 39.1 35.2 46.4
Cis+Dexpc 33.3 26.2 35.1
OSI (µmol H2O2 Eqv/mmol Trolox Eqv) Controla 11.9 7.7 15.6 0.001
Dexpa 9.7 7.8 13.1
Cisb 21.8 20.1 25.9
Cis+Dexpc 15.5 11.5 16.8
IL-1β (pg/ml) Controla 23.3 18.4 42.8 0.081
Dexpa 16.4 12.9 67.7
Cisa 26.8 19.4 63.4
Cis+Dexpa 35.9 20.5 41.7
IL-6 (pg/ml) Controla 13.8 5.8 20.5 0.017
Dexpa 11.7 4.5 20.1
Cisb 28.8 13.8 60.1
Cis+Dexpa 17.1 6.3 34.6
TNF-α (pg/ml) Controla 263.6 167.7 332.4 0.322
Dexpa 237.7 141.5 300.1
Cisa 293.6 219.5 441.6
Cis+Dexpa 242.4 222.4 361.9

Different superscript letters indicate that there is statistical difference between the groups (stepwise step-down multiple comparisons after significant Kruskal Wallis test; P<0.05). a-cSame superscript letters indicate that there is no statistical difference between the groups (P>0.05). Cis, cisplatin; Dexp, dexpanthenol; MDA, malondialdehyde; GSH, reduced glutathione; CAT, catalase; GSH-Px, glutathione peroxidase; Tot Nit, total nitrite; TAS, total antioxidant status; TOS, total oxidant status; OSI, oxidative stress index; ADMA, asymmetric dimethylarginine; SDMA, symmetric dimethylarginine.

Comparison of biochemical parameters measured in serum samples.

Parameters Groups Median Minimum Maximum P
GSH (µmol/l) Controla 15.9 15.7 16,3 0.014
Dexpb 19.2 17.3 19,4
Cisa 15.9 14.3 17,1
Cis+Dexpb 17.7 16.3 19,1
TAS (mmol Trolox Eqv/l) Controla 1.3 1.3 1.3 0.003
Dexpb 1.7 1.4 1.9
Cisc 1.1 1.1 1.1
Cis+Dexpb 1.6 1.4 1.6
TOS (µmol H2O2 Eqv/l) Controla 41.2 38.8 42.8 0.058
Dexpa 35.2 32.4 38.4
Cisa 49.6 33.6 55.6
Cis+Dexpa 44.4 37.6 44.8
OSI (µmol H2O2 Eqv/mmol trolox Eqv) Controla 32.6 30.6 32.9 0.004
Dexpb 20.1 16.8 27.9
Cisa 47.1 30.9 54.3
Cis+Dexpb 27.2 26.9 27.3
Tot Nit (µmol/l) Controla 33.9 32.9 34.8 0.003
Dexpb 45.2 44.3 48.0
Cisa 32.5 31.1 33.9
Cis+Dexpc 36.7 35.8 37.7
L-Arjinin (µmol/l) Controla 0.5 0.3 0.7 0.003
Dexpa 0.4 0.3 0.5
Cisb 6.2 5.8 6.8
Cis+Dexpc 5.5 5.3 5.6
ADMA (µmol/l) Controla 0.2 0,2 0.3 0.026
Dexpa 0.4 0,2 0.4
Cisb 0.5 0,2 0.6
Cis+Dexpa 0.2 0,1 0.3
SDMA (µmol/l) Controla 0.5 0.4 0.5 0.022
Dexpa 0.4 0.3 0.5
Cisb 0.6 0.5 0.7
Cis+Dexpa 0.4 0.4 0.5

Different superscript letters indicate that there is statistical difference between the groups (Stepwise step-down multiple comparisons after significant Kruskal Wallis test; P<0.05).a-cSame superscript letters indicate that there is no statistical difference between the groups (P>0.05). Cis, cisplatin; Dexp, dexpanthenol; GSH, reduced glutathione; TAS, total antioxidant status; TOS, total oxidant status; OSI, oxidative stress index; Tot Nit, total nitrite; ADMA, asymmetric dimethylarginine; SDMA, symmetric dimethylarginine.

Comparison of groups interms of histopathological and immunhistochemical findings.

Parameters Control Dexp Cis Cis+Dexp
Congestion
  Median (min-max) 1.0 (0.0–2.0) 1.0 (0.0–2.0) 1.0 (0.0–3.0)a 1.0 (0.0–3.0)c
  Mean ± SD 0.56±0.58 0.70±0.60 1.13±0.66 1.30±0.60
Glycogen loss
  Median (min-max) 0.0 (0.0–3.0) 0.0 (0.0–3.0) 2.0 (0.0–3.0)a 1.0 (0.0–2.0)b
  Mean ± SD 0.57±0.69 0.49±0.83 2.09±0.65 0.69±0.65
Kupffer cells
  Median (min-max) 1.0 (0.0–5.0) 1.0 (0.0–6.0) 5.0 (0.0–20.0)a 1.0 (0.0–8.0)b
  Mean ± SD 1.35±1.30 1.22±1.50 5.46±3.79 1.63±1.60
Caspase-3 expression
  Median (min-max) 0.0 (0.0–1.0) 0.0 (0.0–1.0) 1.0 (0.0–3.0)a 0.0 (0.0–1.0)b
  Mean ± SD 0.15±0.36 0.33±0.47 1.02±0.85 0.12±0.32

Cis vs. Control group (P<0.001)

Cis vs. Cis+Dex (P<0.001)

Cis vs. Cis+Dex (P<0.079). Cis, cisplatin; Dexp, dexpanthenol.