The Chemoprotective Effect of Fermented Rice Bran on Doxorubicin Induced Toxicity in the Rat
The Chemoprotective Effect of Fermented Rice Bran on Doxorubicin Induced Toxicity in the Rat
Natural Product Sciences. 2014. Mar, 20(1): 29-32
Copyright © 2014, The Korean Society of Pharmacognosy
  • Received : September 25, 2013
  • Accepted : October 27, 2013
  • Published : March 31, 2014
Export by style
Cited by
About the Authors
Keyong Ho, Lee
CKD Pharmaceuticals, Yongin, 446-916 Korea
Ki-Hyeong, Rhee
College of Industrial Sciences, Kongju National University, Yesan 340-702, Korea
Choa Hyung, Cho
College of Environmental & Bioresource Sciences, Chonbuk National University, Iksan 570-752, Korea

In the present study, we examined the chemoprotective effects of different rice bran, which are produced by fermentation or not, on doxorubicin induced rat model, and detected the change of components of rice bran. Rats receiving fermented rice bran of 100 mg/kg by oral plus doxorubicin 10 mg/kg had greater weight gain as +24% than that observed with doxorubicin alone. In case of the treatment of non-fermented rice bran of 100 mg/kg by oral with doxorubicin of 10 mg/kg, fermented rice bran showed a −1.3% decrease in body weight. 100 mg/kg fermented rice bran decreased the incidence to 30%, and non-fermented rice bran decreased the incidence to 50%. In lethality, the rate of death of doxorubicin was 60%. 100 mg/kg fermented rice bran decreased to 10% in death rate and non-fermented rice bran to 30%. In gross gastrointestinal pathology, doxorubicin showed the gross gastrointestinal mucosal pathology in 70% of treated rats, fermented rice bran decreased to 40% and nonfermented rice bran to 50%. In the change of constituent, xylose concentration of fermented rice bran was detected to 59.33 mg/g while its concentration of non-fermented rice bran was 11.12 mg/g.
Chemotherapeutic therapy for cancer is often associated with adverse effects. In the past, chemotherapeutic agents have been selected on the basis of cytotoxicity against cancer cell lines in vitro and in vivo , not on the basis of sophisticated intervention in tumor specific biology. Those cancer drugs, which have toxicity toward tumor cells, share same toxicity with normal cells and tissues. 1 In this adverse effect, chemotherapeutic agents often have gastrointestinal mucosal lesions and hemorrhage, because gastrointestinal mucosal cells are among the most sensitive cells. These often lead to potentially lifethreatening hemorrhage and perforation. 2 Because of these, and pathological effects on other organ systems, there has been great interest in developing concomitant therapy which will protect normal tissue from the effects of chemotherapeutic agents without interfering with their anti-cancer activity.
Rice, and in particular bran rice, contains compounds like tocopherols, tocotrienols, anthocyanins, polyphenols, γ-oryzanol, enzymes, polyunsaturated fatty acids and resistant starch, 3 , 4 which have shown positive effects as modulators of blood pressure, glycemia or serum cholesterol levels. 5 , 6 It may also contain antioxidants that could help in the prevention of tumoral proliferation, 7 , 8 and even nutraceutical prebiotics that could help control colitis by modification of the colonic microbiota. 9 , 10
In the present study, we examined the chemoprotective effect of the fermented rice bran on doxorubicin induced rat model and change of components of rice bran, which will be estimated to show chemoprotective effect, by the fermentation process.
Materials − Defatted rice bran was ( Oryzae sativa ) was obtained by milling brown rice with an Automatic rice tester (SY 94-RAT22400, SsangYong Machinery Co., Ltd., Korea).
Microorganism and inocula Lactobacillus plantarum NCIMB 8826, originally isolated from human intestine, was used for the fermentation of all rice broths. The strain was maintained at 4 ℃ and subcultured monthly on MRS agar slants (Oxoid Ltd, Cambridge, UK). Colonies isolated from MRS agar plates were precultured twice in MRS liquid broth at 37 ℃, first for 24 hours and then for 18 hours, to ensure that all the cells were harvested from the early stationary phase. The bacterial suspensions were then used to inoculate the rice media at 1% (by volume). In all cases, the initial microbial concentration was approx. 7.5 log CFU/mL. 11
Fermentation procedures − Bran was isolated by standard milling process, heat stabilized at 110 ℃ for 5 minutes, and stored at −20 ℃. Shake flask fermentations were performed in duplicate using 500 mL screw-capped glass bottles with 400 mL of medium. Suspensions (3%, by mass per volume) in distilled water were made from the heat stabilized rice bran. The resulting slurry was then autoclaved (15 minutes, 121 ℃) to sterilize the media and to gelatinize the rice bran. Culture media were inoculated and incubated at 150 rpm and 37 ℃ for 48 hours. Fermented product was centrifuged (5,000 g, 10 minutes, 4 ℃) and dried on freezer drier, and stored at –20 ℃ for chemical and biological test. 11
Chemoprotective assay on rat model − Adult male Sprague-Dawley rats (Daehan Laboratory Animals, Korea), weighing 200 - 250 g, were used in all experiments. All animals were maintained at a temperature of 20 ℃ to 23 ℃, and given food (Purina rodent chow, Korea) and water ad libitum . Animals were selected for test based on body weights and randomly assigned (10 rats/group) to each of the following five groups; control, doxorubicin 10mg/kg alone, non-fermented rice bran 100 mg/kg alone, fermented rice bran 100 mg/kg alone, doxorubicin 10 mg/kg plus non-fermented rice bran 100mg/kg and doxorubicin 10 mg/kg plus fermented rice bran 100 mg/kg. All rice brans were administered at one time per day for 5 days by oral. Doxorubicin was treated by intraperitoneal injection at one time per day for 5 days. All groups of rats were observed for signs of gross toxicity and/or behavioral changes daily for 20 days. Consistency of feces was monitored throughout the study. Body weights were recorded on days 0, 5, 10, 15 and 20. On day 20, all animals were euthanized by CO 2 inhalation and necropsied. Gross appearances of major organs of the thoracic and abdominal cavities were evaluated and the presence of gastrointestinal damage was noted. 12
Monosaccharide analysis by HPAEC-PAD − The monosaccharide analysis of TFA-hydrolyzed rice bran was performed by HPAEC (High Performance Anion-Exchange Chromatography) using BioLC (DX 500 Chromatography System, Dionex Co., USA) equipped with pulsed amperometric detector (ED 50, Dionex Co., USA). The dried sample was dissolved in 0.1 ml of dH 2 O and filtered through microspin filters (0.45 μm, PGC Scientifics, Frederick, MD). After the filtration, 20 μL of the sample were injected and fractionated on a CarboPac PA-1 column (4 × 250 mm, Dionex Co., USA) which was preequilibrated with 100 mM NaOH and eluted in an isocratic mode at a rate of 1 ml/min. Arabinose, galactose, glucose and xylose (Sigma Co. St Luis, USA) were used as standard monosaccharides. All the reagents used for rice bran extraction and carbohydrate analysis were of ACS grade. 13
Statistical analysis − Data were presented as mean ± SD. Data were analyzed using analysis of variance (ANOVA) followed by tukey-kramer test for comparison. Statistical significance was defined as p ˂ 0.05.
Results and Discussion
Chemoprotective effect on doxorubicin-induced rat model Fig. 1 shows the effects of treatments on body weight over the duration of the experiment. Animals receiving either fermented rice bran of 100 mg/kg or nonfermented rice bran of 100 mg/kg for 5 daily oral doses showed a typical increase in body weight (+77% in fermented rice bran and +79% in non-fermented one) as normal control group (+85%) while animal receiving doxorubicin 10mg/kg by intraperitoneal showed significant decrease in body weight as −22%. Animal receiving fermented rice bran of 100 mg/kg by oral plus doxorubicin 10 mg/kg by intraperitoneal had greater weight gain as +24% than that observed with doxorubicin alone. In case of the treatment of non-fermented rice bran of 100 mg/kg by oral with doxorubicin of 10 mg/kg by intraperitoneal, fermented rice bran showed a - 1.3% decrease in body weight.
PPT Slide
Lager Image
Effect of fermented and non-fermented rice bran on loss of body weight induced by doxorubicin. Values are expressed as mean ± SD (n = 10).
Effect of fermented and non-fermented rice bran on the occurrence of spontaneous deaths, gross intestinal lesions and diarrhea
PPT Slide
Lager Image
Death: the rate of spontaneous deaths GI Pathology: the rate of the number that showed gross damage to gastrointestinal tract indicated by perforations, hemorrhagic spots Diarrhea: incidence of diarrhea or soft stools Values are expressed as mean ± SD (n = 10) (*: p ˂ 0.05).
In Table 1 , doxorubicin caused deaths in 60% of rats treated. Lethality of doxorubicin was decreased to 10% in rats treated with 100 mg/kg fermented rice bran and 30% in groups treated with non-fermented rice bran as same as dose. Alone treatment of each fermented and nonfermented rice bran did not cause death after a single dose. 100% of rats receiving a single dose of 10 mg/kg doxorubicin showed signs of diarrhea in duration of experiment. 100 mg/kg fermented rice bran decreased the incidence to 30%, and non-fermented rice bran as same dose decreased the incidence to 50%. Doxorubicin produced gross gastrointestinal mucosal pathology in 70% of treated rats. This was decreased to 40% after fermented rice bran and 50% after non-fermented rice bran. Alone treatment of each fermented and non-fermented rice bran did not cause any death, gastrointestinal mucosal pathology and diarrhea.
Monosaccharide analysis by HPAEC-PAD − Monosaccharide composition analyses of fermented and nonfermented rice bran were performed by HPAEC/PAD analysis after 2M TFA hydrolysis in Table 2 . Each monosaccharide was quantified by comparing the peak area of sample sugar to that of standard monosaccharide of known amount. The change of xylose concentration in fermented rice bran was mainly occurred. Xylose concentration was detected to 59.33 mg/g while its concentration of non-fermented rice bran was 11.12 mg/g. The concentration of the others was not greatly changed between two samples.
Two different rice bran, which were fermented and non-fermented rice bran, were shown in this study to protect rats given an acutely toxic dose of doxorubicin. The endpoints chosen for evaluation were prevention of the effects of these samples on body weight, stool consistency, gross pathology of the gastrointestinal tract and mortality. Significant protection was observed on body weight. Protection against gastrointestinal mucosal lesions and diarrhea were also observed, as was a decreased mortality due to doxorubicin, even if it is not clear from this study whether this was due to increased food intake or prevention of the catabolic effects of the chemotherapeutic agent. Fermented rice bran appeared to be more effective than non-fermented thing according to experimental data such as body weight, death, gross gastrointestinal pathology and diarrhea. It is assumed that it came from the change of monosaccharide by fermentation, specifically increased the concentration of xylose, which is one of the major components form hemicelluloses and arabinoxylan. It is assumed that rice bran was changed to active form that appears to prevent the toxicity by fermentation.
Monosaccharides concentration of fermented and nonfermented rice bran
PPT Slide
Lager Image
Values are expressed as mean ± SD (n = 5) (*: p ˂ 0.05).
Doxorubicin produces well-documented pathology when used as chemotherapy for malignant diseases. 14 Severe cardiac and renal pathology are common. This study was not designed to evaluate these adverse effects since the dose of doxorubicin was not sufficient to produce significant pathologic changes in the liver. However, there were signs of gross pathology when gastrointestinal mucosa was evaluated. The mechanism by which rice bran protects against the toxicity of doxorubicin is unknown. Rice bran has been reported to have a chemopreventive effect, 15 and to increase NO production, cytokines and radio-protection relating to immunestimulation. 16 , 17
There is still a great need for non-toxic agents that have significant protective effect against chemotherapy induced adverse effects. 1 Further study on the mechanism is needed. In conclusion, rice bran, specifically fermented rice bran by Lactobacillus plantarum , appears to be effective in protection against some of the disturbing side effects produced by doxorubicin and may be valuable in improving quality of life in patients receiving chemotherapy. Fermented rice bran may prove to be useful as an adjunct to cancer thermotherapy.
Hoekman K. , van der Vijgh W.J. , Vermorken J.B. 1999 Drugs 57 133 - 155    DOI : 10.2165/00003495-199957020-00002
Hirakawa M. , Iida M. , Aoyagi K. , Matsui T. , Akagi K. , Fujishima M. 1988 Am J Gastroenterol. 83 837 - 840
Hagiwara H. , Seki T. , Ariga T. 2004 Biosci. Biotechnol. Biochem. 68 444 - 447    DOI : 10.1271/bbb.68.444
Jariwalla R.J. 2001 Drugs Exp. Clin. Res. 27 17 - 26
Li G. , Qu M. , Wan J. , You J. 2007 Asia Pac. J. Clin. Nutr. 16 275 - 280
Murata K. , Kamei T. , Toriumi Y. , Kobayashi Y. , Iwata K. , Fukumoto I. , Yoshioka M. 2007 Clin. Exp. Pharm. Phys. 34 (Suppl. 1) 87 - 89    DOI : 10.1111/j.1440-1681.2007.04790.x
Hudson E.A. , Dinh P.A. , Kokubun T. , Simmonds M.S.J. , Gescher A. 2000 Cancer Epidem. Biomar. Prev. 9 1163 - 1170
Parrado J. , Miramontes E. , Jover M. , Gutierrez J.F. , Collantes de Teran L. , Bautista J. 2006 Food Chem. 98 742 - 748    DOI : 10.1016/j.foodchem.2005.07.016
Kataoka K. , Kibe R. , Kuwahara T. , Hagiwara M. , Arimochi H. , Iwasaki T. , Benno Y. , Ohnishi Y. 2007 Anaerobe 13 220 - 227    DOI : 10.1016/j.anaerobe.2007.07.001
Kataoka K. , Ogasa S. , Kuwahara T. , Bando Y. , Hagiwara M. , Arimochi H. , Nakanishi S. , Iwasaki T. , Ohnish Y. 2008 Dig. Dis. Sci. 53 1601 - 1608    DOI : 10.1007/s10620-007-0063-3
Saman P. , Fucinos P. , Vazquez J.A. , Pandiella S.S. 2011 Food Technol. Biotechnol. 49 128 - 132
Johnsson A. , Wennerberg J. 1999 Acta Oncol. 38 247 - 253    DOI : 10.1080/028418699431681
Lee Y.K. , Lim D.J. , Lee Y.H. , Park Y.I. 2006 Algae 2 157 - 160
Links M. , Lewis C. 1999 Drugs 57 293 - 308    DOI : 10.2165/00003495-199957030-00003
Phutthaphadoong S. , Yamada Y. , Hirata A. , Tomita H. , Taguchi A. , Hara A. , Limtrakul P.N. , Iwasaki T. , Kobayashi H. , Mori H. 2009 Oncol. Rep. 21 321 - 327
Park H.Y. , Yu A.R. , Choi I.W. , Hong H.D. , Lee K.W. , Choi H.D. 2013 Int. Immunopharmacol. 17 191 - 197    DOI : 10.1016/j.intimp.2013.06.013
Ghoneum M. , Badr El-Din N.K. , Abdel Fattah S.M. , Tolentino L. 2013 J. Radiat. Res. 54 419 - 429    DOI : 10.1093/jrr/rrs119