Ratlarda Gentamisin İle İndüklenmiş Oksidatif Streste Borun Muhtemel Koruyucu Etkisinin Dokularda Araştırılması#
Çalışmada gentamisin maruziyeti ile toksisite oluşturulan ratlarda borun (B) muhtemel koruyucu etkisinin belirlenmesi amaçlandı. Bu amaçla Wistar albino 56 erkek rat kullanıldı. Her grupta 7 hayvan olacak şekilde, kontrol, gentamisin (100 mg/kg i.p.), B-5 (5 mg/kg B, i.p.), B-10 (10 mg/kg B, i.p.), B-20 (20 mg/kg B, i.p.), B-5 + gentamisin (5 mg/kg B ve 100 mg/kg gentamisin, i.p.), B-10 + gentamisin (10 mg/kg B ve 100 mg/kg gentamisin, i.p.), B-20 + gentamisin (20 mg/kg B ve 100 mg/kg gentamisin, i.p.) olarak 8 gruba ayrıldı. Ratlara B uygulaması gentamisin enjeksiyonundan 4 gün önce verilmeye başlandı. Gentamisin uygulamasına 4. gün başlandı ve 12. gün bu uygulama sonlandırıldı. Gentamisin uygulamasının bitişinden itibaren hayvanlara 2 gün daha B verildi. Uygulama sonunda hayvanlardan anestezi altında karaciğer, kalp, beyin, akciğer ve testis dokuları alındı. Gentamisinin karaciğer dokusunda malondialdehid düzeylerini arttırdığı, buna karşın redükte glutatyon düzeylerini, superoksid dismutaz ve katalaz aktivitelerini azalttığı tespit edildi. Histopatolojik incelemede gentamisinin dokularda hasar oluşturduğu gözlendi. Buna karşın, B uygulamasının gentamisin ile indüklenen hasarı azalttığı tespit edildi.
Potential Protective Effect of Boron Against Gentamicin-Induced Oxidative Stress on Rat Tissues
The objective of this study was to determine the protective effects of boron on gentamicin induced toxicity in rats. Rats were divided into eight experimental groups containing seven animals in each group. Experimental groups were as follows; control group (fed without B), gentamicin group (100 mg/kg, i.p.), B-5 group (5 mg/kg B, i.p.), B-10 group (10 mg/kg B, i.p.), B-20 group (20 mg/kg B, i.p.), B-5 + gentamicin group (5 mg/kg B and 100 mg/kg gentamicin, i.p.), B-10 + gentamicin group (10 mg/kg B and 100 mg/kg gentamicin, i.p.), and B-20 + gentamicin group (20 mg/kg B and 100 mg/kg gentamicin, i.p.). B was given to rats before four days. Gentamicin was given to rats on the fourth day and finished on the twelfth day. Also, administration of B was completed the fourteenth day. End of the experiment, liver, hearth, brain, lung, and testis tissues were collected from animals under anaesthesia. Administration of gentamicin increased malondialdehyde levels whereas decreased reduce glutathione levels, superoxide dismutase and catalase activities in the liver. Histopathologically, damages were detected in the tissues of gentamicin group. However, treatment of boron resulted in a reversal of gentamicin-induced damages.
___
- Aebi H. Catalase in vitro, in: U. Bergmeyer (Ed.),
Methods of enzymatic analysis. Academic
Press, New York and London. 1974; 673-
677.
- Atessahin A, Karahan I, Yilmaz S, Çeribaşi AO,
Princci I. The effect of manganese chloride
on gentamicin-induced nephrotoxicity in
rats. Pharmacological Research. 2003; 48:
637-642.
- Beutler E, Duron O, Kelly BM. Improved
method for the determination of blood
glutathione. Journal of Laboratoty and
Clinical Medicine. 1993; 61: 882-888.
- Bilgiç M, Dayık M. Borun özellikleri ve tekstil
endüstrisinde kullanımıyla sağladığı
avantajlar. Tekstil Teknolojileri Elektronik
Dergisi. 2013; 7: 27-37.
- Bourgeois AC, Scott ME, Sabally K, Koski KG.
Low dietary boron reduces parasite
(nematoda) survival and alters cytokine
profiles but the infection modifies liver
minerals in mice. Journal of Nutrition. 2007;
137: 2080-2086.
- Briggs GG, Ambrose P, Nageotte MP.
Gentamicin dosing in postpartum women
with endometritis. American Journal of
Obstetrics and Gynecology. 1989; 160: 309-
13.
- Cuzzocrea S, Mazzon E, Dugo L, Serraino I,
Di Paola R, Britti D, De Sarro A,
Pierpaoli S, Caputi A, Masini E,
Salvemini DA. Role for superoxide in
gentamicin-mediated nephropathy in rats.
European Journal of Pharmacology. 2002;
450: 67-76.
- Dökmeci İ, Akçasu A, Banoğlu N, Berkarda Ş.
Farmakoloji. İlaç Uygulamalarında Temel
Kavramlar. Editör: Dökmeci İ. Nobel Tıp
Kitabevleri. 1992; 705-785.
- Duff P, Jorgensen JH, Gibbs RS, Blanco JD,
Alexander G, Castaneda YS. Serum
gentamicin levels in patients with postcesarean
endomyometritis. Obstetric
Gynecology. 1983; 61: 723-727.
- Hancock RE, Raffle VJ, Nicas TI. Involvement
of the outer membrane in gentamicin and
streptomycin uptake and killing in
Pseudomonas aeruginosa. Antimicrobial Agents
Chemotheraphy. 1981; 19: 777-785.
- Ince S., Arslan-Acaroz D. An Update on Health
Effects of Metalloid Trace Element: Boron.
Aperito Journal of Drug Designing and
Pharmacology. 2015; 2:1.
- Ince S, Keles H, Erdogan M, Hazman O,
Kucukkurt I. Protective effect of boric acid
against carbon tetrachloride–induced
hepatotoxicity in mice. Drug and chemical
toxicology. 2012; 35: 285-292.
- Ince S, Kucukkurt I, Cigerci IH, Fidan AF,
Eryavuz A. The effects of dietary boric acid
and borax supplementation on lipid
peroxidation, antioxidant activity, and DNA
damage in rats. Journal of Trace Element
and Medicinal Biology. 2010; 24: 161-164.
- Ince S, Kucukkurt I, Demirel HH, Acaroz DA,
Akbel E, Cigerci IH. Protective effects of
boron on cyclophosphamide induced lipid
peroxidation and genotoxicity in
rats. Chemosphere. 2014; 108: 197-204.
- Karahan I, Atessahin A, Yılmaz S, Ceribası AO,
Sakin F. Protective effect of lycopene on
gentamicin-induced oxidative stress and
nephrotoxicity in rats. Toxicology. 2005;
215: 198-204.
- Kayaalp SO. Rasyonel Tedavi Yönünden Tıbbi
Farmakoloji (Cilt 3). Ankara: Feryal
Matbaası. 1990.
- Khan MR, Badar I, Siddiquah A. Prevention of
hepatorenal toxicity with Sonchus asper in
gentamicin treated rats. BMC
complementary and alternative
medicine. 2011; 11(1): 113.
- Khan SA, Priyamvada S, Farooq N, Khan S,
Khan MW, Yusufi AN. Protective effect of
green tea extract on gentamicin-induced
nephrotoxicity and oxidative damage in rat
kidney. Pharmacological Research. 2009; 59:
254-262.
- Kucukkurt I, Akbel E, Karabag F, Ince S. The
effects of dietary boron compounds in
supplemented diet on hormonal activity and
some biochemical parameters in
rats. Toxicology and industrial health. 2015;
31: 255-260.
- Kucukkurt I, Ince S, Fidan AF, Ozdemir A.
The effects of dietary supplementation of
different amount of Yucca schidigera powder
(Sarsaponin 30®) on blood and tissue
antioxidant defense systems and lipid
peroxidation in rats. Journal of Animal and
Veterinary Advances. 2008; 7: 1413-1417.
- Lode H, Kemmerich B, Koeppe P. Comparative
clinical pharmacology of gentamicin,
sisomicin, and tobramycin. Antimicrobial
Agents Chemotheraphy. 1975; 8: 396-401.
- Lowry OH, Rosebrough NJ, Farr AL, Randall
RJ. Protein measurement with the Folin
phenol reagent. The Journal of Biological
Chemistry. 1951; 193: 265-275.
- Luo QH, Chen ML, Sun FJ, Chen ZL, Li MY,
Zeng W, Gong L, Cheng AC, Peng X,
Fang J, Tang L, Geng Y. KIM-1 and
NGAL as biomarkers of nephrotoxicity
induced by gentamicin in rats. Moleculer
Cell Biochemistry. 2014; 397: 53-60.
- McCoy H, Kenney MA, Montgomery C, Irwin
A, Williams L, Orrell R. Relation of boron
to the composition and mechanical
properties of bone. Environmental Health
Perspective. 1994; 102: 49-53.
- Nakajima T, Hishida A, Kato A. Mechanisms
for protective effects of free radical
scavengers on gentamicin-mediated
nephropathy in rats. American Journal of
Physiology. 1994; 266: 425-431.
- Nielsen FH, Hunt CD, Mullen LM, Hunt JR.
Effect of dietary boron on mineral,estrogen,
and testosterone metabolism in
postmenopausal women. Faseb Journal.
1987; 1: 394-397.
- Noorani AA, Gupta K, Bhadada K, Kale MK.
Protective effect of methanolic leaf extract
of Caesalpinia bonduc (L.) on gentamicininduced
hepatotoxicity and nephrotoxicity in
rats. Iranian Journal of Pharmacology and
Therapeutics. 2011; 10: 21-25.
- Ohkawa H, Ohishi N, Yagi K. Assay for lipid
peroxides in animal tissues by thiobarbituric
acid reaction. Analytical Biochemistry. 1979;
95: 351-358.
- Quirós Y, Vicente-Vicente L, Morales AI,
Lopez-Novoa JM, Lopez-Hernandez FJ.
An integrative overview on the mechanisms
underlying the renal tubular cytotoxicity of
gentamicin. Toxicological Sciences. 2011;
119: 245–256.
- Samman S, Naghii MR, Lyons Wall PM, Verus
AP. The nutritional and metabolic effects of
boron in humans and animals. Biological
Trace Element Research. 1998; 66: 227-235.
- Sun Y, Oberley LW, Li Y. A simple method for
clinical assay of superoxide dismutase.
Clinical Chemistry. 1988; 34: 497-500.
- Şanlı Y, Kaya S. Veteriner Farmakoloji ve İlaçla
Sağıtım Seçenekleri. Medisan Yayınevi,
Ankara. 1994; 571-650.
- Şener S. Veteriner Klinik Farmakoloji ve
Formüller. Pethask Veteriner Hekimliği
Yayınları. 1990; 83-91.
- Turkez H, Geyikoğlu F, Tatar A, Keleş S,
Özkanç A. Effects of some boron
compounds on peripheral human blood.
Zeitschrift für Naturforschung. 2007; 62:
889-896.