The effect of curcumin as an antioxidant on cochlea fibroblasts in ototoxic rat models

  

Journal of Chinese Pharmaceutical Sciences http://www.jcps.ac.cn

The effect of curcumin as an antioxidant on cochlea fibroblasts in ototoxic

rat models

  1*

  1

  1 Tengku Siti Hajar Haryuna , Agustinus Hamonangan Winston Purba , Farhat Farhat ,

  2 Soehartono Taat Putra

  1. Department of Otorhinolaryngology, Faculty of Medicine,Universitas Sumatera Utara, Medan 20155, Indonesia

  

2. Pathobiology Division, Department of Anatomic Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya 60131, Indonesia

Abstract: Aminoglycosides (e.g. Gentamicin) are ototoxic drugs and widely prescribed due to their effective antimicrobial

  actions and affordable prices. This study focused on determining protective effect of curcumin against the damage caused by aminoglycosides. We aimed to demonstrate the potential of curcumin as an antioxidant to increase the expressions of superoxide dismutase (SOD) in fibroblasts of cochlea lateral wall in ototoxic rat models. The experiment was conducted with randomized _{-only control group design by using 32 male Rattusnorvegicus adults which received a combination of gentamicin and} post test curcumin with different durations and doses. Then, the rats underwent terminations and immunohistochemical assay to determine the expression of SOD. The rats receiving gentamicin injection showed significantly decreased expression of SOD ( P<0.05), and the administration of curcumin before and after the gentamicin injection showed significantly increased expression of SOD (P<0.05). Collectively, we showed that curcumin was an antioxidant against oxidative stress due to ototoxicity evidenced by the expression of SOD.

  Keywords: Curcumin; Antioxidant; Gentamicin; Superoxide dismutase; Preventive; Rat; Experimental CLC number: R965 Document code: A Article ID: 1003–1057(2018)12–847–08

  incidence rate is varied greatly due to the differences

  1. Introduction [3] in study designs and methodologies .

  The integrity and functional wall of the cochlea lateral Aminoglycosides are ototoxic drugs, which are widely play a role in the formation of potential endo -coccal and prescribed due to their effective antimicrobial action and

  [1]

www.jcps.ac.cn

  ion homeostatic arrangements in the inner ears . The

  [4]

  affordable prices . The local administration of gentamicin research on the lateral wall of the cochlea is still very may cause ototoxicity which is not selective in the view, and this becomes the motivation for the researchers

  [5]

  cochlea and vestibular hair cells . Aminoglycosides, to conduct a research about lateral wall of the cochlea. such as gentamicin, are classified as basic drugs used to

  The sense of hearing has an important role in social eliminate Gram -negative bacterial infections. However, relationships, and one of the causes of hearing loss is gentamicin itself can cause permanent damage to the ototoxic medication. One type of drugs that can

  [6] sensory hair cells in humans and mammals .

  cause ototoxicity is gentamicin, an aminoglycoside Aminoglycosides possess the ability to form an active

  [2]

  antibiotic . The incidence of cochlea damage caused metabolite that can catalyse the production of reactive by aminoglycoside is equal to 7%–90%, and the oxygen species (ROS), a highly reactive compound.

  Human body has a defence system against ROS in the

• _* Received: 2018 -09-27, Revised: 2018-10-15, Accepted: 2018-11-05.

  Corresponding author. Tel.: +62 -8126061694

  form of antioxidant agents, namely superoxide dismutase,

  E -mail: tengkusitihajarharyuna@gmail.com [7] http://dx.doi.org/10.5246/jcps.2018.12.086 glutathione and catalase .

  Curcuma longa L. is a plant originally grows in Asia,

  [15] .

  [8] .

  Moreover, it is commonly used as a cooking spice and food dye

  [9]

  . A dose of curcumin up to 8 g/d is known to have no side effects in the first phase of clinical trials

  [10]

  . Other benefits exhibited by curcumin include antioxidant, antihepatotoxic, antitumor and antirheumatic activities

  [11]

  . Curcumin scavenges the oxygen to free radicals and inhibits lipid peroxidation, as well as protects cellular macromolecules, including DNA, against oxidative damage

  [12] .

  This study aimed to demonstrate the potential of curcumin as an antioxidant to increase the expressions of SOD (superoxide dismutase) on fibroblasts of cochlea lateral wall in ototoxic rat models, which could be used as the basis for further clinical practice.

  and its rhizome has anti _{-inflammatory properties}

  The ethical permission to conduct this research was approved from the Health Research Ethical Committee, Medical Faculty of Universitas Sumatera Utara/H. Adam Malik General Hospital, Medan, Indonesia, with the code number 433/KOMET/FK USU/2015.

  The samples drawn in this study were rats which were in the same strain, homogeneous in regards to their gender and ages, and rats were bred in the laboratory of Biochemistry, Faculty of Medicine, Airlangga University. The meals for the rats were provided ad libitum, the room temperatures for the rats in the laboratory were between 20 ºC to 26 ºC, the lighting inside the cages during the light phase was maintained at the exposure below the reluctance threshold for the rats, and the relative ambient humidity was 55%±15%.

2. Material and methods

  After the rats calmed down, they were injected with 0.03–0.05 cc of 40 mg/mL of gentamicin

  [14]

  , and in this study, the dose of 0.1 cc was injected to the anterosuperior tympanic membrane of the rats with the help of microscope. The rats were terminated for 18 h after the gentamicin injection

  [13] .

  , which was suspended in CMC/carboxy methyl cellulose 0.5% and given through nasogastric tube. There were groups given 200 mg/kg of curcumin to analyze the effect of twice doses of the curcumin. The rats were first anesthetized by using 10 mg/kg of xylazine and 90 mg/kg of ketamine through intraperitoneal injection

  [13]

  The rats studied in this research were divided into eight groups. The Group 1 was the control group which was not treated and only given 5 cc of CMC. The Group 2 (positive control group) was injected with gentamicin and terminated for 18 h afterwards. The Group 3 was injected with gentamicin, and after 18 h the rats were given 20 mg of curcumin, followed by termination 18 h later. The Group 4 was injected with gentamicin, and after 18 h the rats were given 40 mg of curcumin, followed by termination 18 h later. The Group 5 was injected with gentamicin, after 18 h the rats were given curcumin for 7 d with the dose of 20 mg per day, and rats were sacrificed at 18 h after the last curcumin dose. The rats studied in Group 6 were injected with gentamicin, after 18 h they were given curcumin for 7 d with the dose of 40 mg per day, and rats were sacrificed at 18 h after the last curcumin dose.

  www.jcps.ac.cn

  A total of 32 male rats, Rattusnorvegicus type, weighing 150–250 g, were used in the present study. The rats were evenly divided into eight groups. The curcumin given to the rats was the extracted from Curcuma longa L (Turmeric, certificate number 0632/SA/V/2016, certified by Dr. rer. Nat. M. Yuwono, MS. in Pharmacy Faculty Universitas Airlangga). The level of curcumin was 16.62%±0.14% b/b counted through TLC _{-densitometric method. The curcumin dose was} 100 mg/kg

• –1.500±1.013
• –1.750±1.013
• –2.750±1.013
• –3.000±1.013 0.036 ^* 1.000 1.000 0.152 0.097

  5

  6

  7

  8

  3

  4

  5

  6

  7

  8 0.000±1.013

  6

  4

  7

  8

  5

  6

  7

  8

  6

  7

  8

  7 8 –0.250±1.013 0.807 Table 1. ANOVA test results in regards of the expression of SOD.

  5

  3

  www.jcps.ac.cn

  0.012 ^* 0.007

• ^* 2

  The rats studied in Group 7 were given 20 mg of curcumin per day for 3 d and injected with gentamicin at 18 h after the last curcumin dose, and rats were sacrificed 18 h later. The rats studied in Group 8 were given 40 mg of curcumin per day for 3 d and given gentamicin injection at 18 h after the last curcumin dose, and rats were sacrificed 18 h later.

  The rats were terminated and examined through necropsies, and the temporal bone tissues from their heads were collected. The samples of the tissues were fixed with 10% of formalin buffer solution, decalcified with EDTA for 4 weeks and tested in the laboratory to assess the apoptotic index on the lateral wall of cochlear fibroblasts.

  2.1. Immunohistochemical assay

  All samples were immunohistochemically examined for the expression of SOD in cochlear fibroblasts using a primary antibody (polyclonal anti _{-SOD1 antibodies} (Boster Biological Technology Co. Ltd. Cat #: 1345)). The expression of SOD was investigated by using Olympus XC 10 microscope under 100× magnifications, marked by brown

• _{-stained cytoplasm. The countings} were performed by two investigators, a researcher and a pathologist, with double blind method. The expression of SOD was evaluated in width (P) and intensity (I) of brown staining in cytoplasm. Intensity score: 1–3, width score 0: 0%; 1, <10%; 2, 10%–50%; 3, >50% and immune _{-reactive score P×I, resulted}

  0–9

  [16] .

  2.2. Statistical analysis

  The data were analyzed with One -way ANOVA by using IBM SPSS Statistics with significance level of 0.05.

  3. Results

  3.1. The expression of SOD

  The effects of curcumin on cochlear lateral walls of ototoxic rat models were assessed by IHC. We assessed the expression of SOD by width and intensity of the brown

• _{-stained cytoplasms (immune-reactive} score) (Table 1). Group given gentamicin without curcumin (Fig. 1B) showed the weakest expression of SOD compared with other group given curcumin (Fig. 1C–H). Prevention group (Fig. 1G–H) showed the strongest expression of SOD compared with group given gentamicin and curcumin (Fig. 1C–F).

  Group Mean difference±Standard deviation P value

  1

  2

  3

  4

  5

  6

  7

  8 2.250±1.013 0.000±1.013 0.000±1.013

• –2.250±1.013
• –2.250±1.013
• –3.750±1.013
• –4.000±1.013
• –5.000±1.013
• –5.250±1.013 0.036 ^* 0.036 ^* 0.001 ^* 0.001 ^* 0.000
• ^* 0.000 ^*
• –1.500±1.013
• –1.750±1.013
• –2.750±1.013
• –3.000±1.013 1.000 0.152 0.097 0.012 ^* 0.007
• ^* 4
• –1.500±1.013
• –1.750±1.013
• –2.750±1.013
• –3.000±1.013 0.152 0.097 0.012 ^* 0.007 ^*
• –0.250±1.013
• –1.250±1.013
• –1.500±1.013 0.807 0.229 0.152
• –1.000±1.013
• –1.250±1.013 0.333 0.229
• Denotes statistically significant.
In this study, we analyzed the antioxidant activity of curcumin and assessed the expression of SOD in fibroblasts of ototoxic rat models.

  The results of this study showed that the comparison between Groups 1 and 2 (positive control group) exhibited the statistically significant result, implying that gentamicin decreased the expression of SOD in fibroblasts of cochlea lateral wall. The similar changes were observed in melanocyte cells exposed to gentamicin, leading to significant changes in the cellular antioxidant enzymes: SOD, CAT and GPx, indicating the depletion of antioxidant defense system

  [17]

  . Gentamicin used was 40 mg/mL, and the same gentamicin dose was used as the ototoxic control in the middle ears of Wistar Albino rats

  [14] .

  The rats were terminated at 18 h after they were given gentamicin injection in accordance with the results conducted on the Hartley strain guinea pig, in which the administration of gelatin sponge soaked in gentamicin at the round window membrane after 18 h shows the highest cell death markers

  [15] .

  The curcumin is given to the rats once per day for 7 d, which can effectively increase the SOD expression in rats

  [13] . Therefore, we implemented the same method.

  

Figure 1. The expression of SOD (100× zoom): (A) Group 1; (B) Group 2; (C) Group 3; (D) Group 4; (E) Group 5; (F) Group 6; (G) Group 7;

(H) Group 8. The black arrow indicates the expression of SOD in cochlear fibroblasts marked by the brown -stained cytoplasm.

  (A) (B) (C) (D) (E) (F) (G) (H) www.jcps.ac.cn

4. Discussion

  [17] . www.jcps.ac.cn

  [25] .

  A general mechanism for the generation of ROS is the Fenton reaction: Fe

  2+

  2 O

  2

  → Fe

  3+

  ·

  When gentamicin reacts with iron salts, the gentamicin _- iron complex enhances iron -catalyzed oxidations and directly promotes the generation of ROS. In this process, unsaturated fatty acid acts as an electron donor. In turn, fatty acids, predominantly arachidonic acid, are oxidized to lipid peroxides. Since arachidonic acid is an essential fatty acid in cellular membranes, ROS can affect membrane fluidity and permeability. Through lipid peroxidation, ROS can influence nucleid proteins and acids, thereby disrupting the activity of enzymes, ion channels and receptors. If the formation of ROS exceeds the capacity of the repair and intrinsic protective systems, the cells undergo apoptosis

  The identification of the sensorial cell and organ of Corti endogenous defense mechanisms is in the form of antioxidant and detoxification enzymes SOD, catalase, glutathione peroxidase (GPx), reductase and glutathione S _-transferase

  The transtympanic route shows ototoxic damage in many species

  [26]

  . SOD converts superoxide anion radical (O

  2 ·–

  ) into hydrogen peroxide (H

  2 O

  2

  ), and then hydrogen peroxide into highly reactive radical hydroxil (OH

  ·–

  ), or can be converted into water by the enzyme catalase or GPx. The use of gentamicin at high concentration may induce the decrease of antioxidant defense system

  [24] .

  [17] .

  The results showed that the administration of curcumin enhanced the expression of SOD in fibroblasts of cochlea lateral wall in ototoxic rat models as seen in the comparison between Group 2 and Groups 3, 4, 5, 6. The similar result has been found in a study of Drosophila where the increased activity of SOD is observed on Drosophila receiving curcumin compared with those without curcumin administration

  Excessive ROS levels trigger the apoptotic pathway, which then produces cell death caused by aminoglycoside - induced ototoxicity. Although aminoglycoside _-induced ototoxicity is well -documented, its molecular mechanisms still have not been precisely determined

  [18]

  . The increased activity of SOD is also observed in a study in brain regions in rats receiving lead and curcumin compared with the group receiving lead only

  [19]

  . The curcumin dose is 100 mg/kg and this curcumin dose has been proven to effectively reduce cell death markers in rats undergoing hepatectomy

• – .
• H
• HO
• HO

  [23] .

  There is no safe dose of aminoglycoside through any route of administrations (intravenous, intratympanic, oral and intrathecal)

  [22] .

  Aminoglycosides, including gentamicin, are antibiotics widely used to eliminate Gram

• _{-negative bacterial infections,} which have become popular again due to increased prevalence of _{antibiotic resistance in other classes}

  Curcumin extracted from Curcuma longa L. is widely available in Asia as a food seasoning, coloring and flavoring

  The results showed that curcumin had a preventive effect as shown in Groups 7 and 8. The similar result has been found in a study conducted on rats, where SOD activity is higher in the group receiving curcumin before the administration of acetaminophen compared with the acetaminophen -administered group only

  In this study, the curcumin was given for 3 d. Curcumin is a potent inhibitor toward the formation Utara No: 120/SP2H/PL/Dit. Litabmas/II/2015, on of ROS and also a potent scavenger against a variety February 5 2015 for the financial support. The authors

  [20] .

  . A single dose of curcumin is enough to show the antioxidative effect

  [13]

  [12]

  . Curcumin has many pharmacological benefits, including antioxidant, anti -inflammatory, and anticancer activities

  [23] .

  Aminoglycosides _{-induced ototoxicity is developed} from low frequency to high frequency and associated with oxidative stress. Aminoglycosides, e.g. gentamicin, can react with iron to form ROS in the inner ear, inflicting permanent damage to hair cells and neurons.

  [21] .

  ·–

  of ROS, including superoxide anion radicals (O ) also would like to thank Biochemisty Laboratory, Faculty

  2 ·–

  and hydroxil radical (OH ). Curcumin enhances the of Medicine, Universitas Airlangga Surabaya; Anatomic activity of antioxidant enzyme SOD by nuclear factor Pathology Laboratory, Faculty of Medicine, Dr. Soetomo

  [27]

  erythroid -derived 2 (Nrf2) . Curcumin has the role of ROS General Hospital Surabaya; Biochemistry Laboratory,

  ·–

  scavenger against superoxide anions (O ) and hydrogen Faculty of Medicine, Universitas Brawijaya Malang, for

  2 [28]

  peroxide (H O ) and it can increase the antioxidant providing equipment and scientific apparatus.

  2

  2 [28–30]

  activity of SOD , catalase, glutathione peroxydase,

  [28] heme oxygenase -1 and glutathione transferase .

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