Efecto del extracto de Boswellia serrata sobre el daño testicular inducido por Metotrexato

  • Gözde Arkalı Fırat University, Faculty of Veterinary Medicine, Department of Physiology. Elazığ, Turkey
  • Tutku Can Acısu Fırat University, Faculty of Veterinary Medicine, Department of Reproduction and Artificial Insemınation. Elazığ, Turkey
  • Nida Badıllı Fırat University, Faculty of Veterinary Medicine, Department of Reproduction and Artificial Insemınation. Elazığ, Turkey
  • Edanur Güler–Ekmen Fırat University, Faculty of Veterinary Medicine, Department of Physiology. Elazığ, Turkey
  • Osman Sedat Tanyeri Fırat University, Faculty of Veterinary Medicine, Department of Physiology. Elazığ, Turkey
  • Abdullah Toz Fırat University, Faculty of Veterinary Medicine, Department of Physiology. Elazığ, Turkey
  • Mehmet Çay Firat University, Faculty of Veterinary Medicine, Department of Physiology, Elazig, Turkey
  • Abdurrauf Yüce Fırat University, Faculty of Veterinary Medicine, Department of Physiology. Elazığ, Turkey
  • Mesut Aksakal Fırat University, Faculty of Veterinary Medicine, Department of Physiology. Elazığ, Turkey
Palabras clave: Extracto de Boswellia serrata, metotrexato, lesión testicular, semen, estrés oxidativo

Resumen

El objetivo fue determinar el efecto del extracto de Boswellia serrata sobre el daño testicular inducido por metotrexato mediante la evaluación del sistema antioxidante, el peso de los órganos reproductores, algunos parámetros espermatológico y los niveles de testesterona sérica en este estudio. Para ello, 40 ratas Sprague Dawley se dividieron en 4 grupos. 1. Grupo Control (n=10): No se aplicó ningún tratamiento durante 10 días. 2. Grupo de B. serrata (n=10): B. serrata se administró a una dosis de 500 mg·kg-1 por sonda durante 10 días. 3. Grupo de metotrexato (n=10): el metotrexato se administró por vía intraperitoneal en una dosis única de 20 mg·kg-1. 4. Grupo de metotrexato + B. serrata (n = 10): el metotrexato se administró por vía intraperitoneal en una dosis única de 20 mg·kg-1, luego se administró 500 mg·kg-1 de B. serrata por sonda durante 10 días. Se determinó que B. serrata aumentó significativamente el nivel de testosterona en suero (P<0,001), el nivel de GSH en los testículos (P<0,001) , la motilidad de los espermatozoides (P<0,001), la concentración de espermatozoides (P<0,001), el peso absoluto de los órganos de la próstata ventral (P<0,001) de las vesículas seminales (P<0,05) en el grupo de metotrexato + B. serrata, La disminución en el nivel de MDA de los testículos (P>0,05) y el aumento en la actividad de la enzima GSH–Px de los testículos (P>0,05) y el peso corporal final (P>0,05) no fueron significativos en el grupo de metotrexato + B. serrata en comparación con el grupo de metotrexato. En conclusión, los efectos negativos del metotrexato en el sistema reproductivo masculino pueden reducirse administrando extracto de B. serrata.

Descargas

La descarga de datos todavía no está disponible.

Citas

Schilsky RL. Methotrexate: An effective agent for treating cancer and building careers. The polyglutamate era. Stem Cells. [Internet]. 1996; 1(4):244–247. doi: https://doi.org/k4pd

Ede AEV, Laan RF, Blom HJ, De Abreu RA, Van De Putte. Methotrexate in rheumatoid arthritis: an update with focus on mechanisms involved in toxicity. Seminars in Arthritis Rheumatism. [Internet]. 1998; 27(5):277–292. doi: https://doi.org/b644pk

Kishi T, Tanaka Y, Ueda K. Evidence for hypomethylation in two children with acute lymphoblastic leukemia and leukoencephalopathy. Cancer. [Internet]. 2000; 89 (4):925–931. doi: https://doi.org/d39chz

Gaies E, Jebabli N, Trabelsi S, Salouage I, Charfi R, Lakhal M, Klouz A. Methotrexate side effects: review article. J. Drug Metabol. Toxicol. [Internet]. 2012; 3(4):1–5.doi: https://doi.org/k4pf

Braun J. Optimal administration and dosage of methotrexate. Clinic. Experim. Rheumatol. 2010; 28(5):46–51.

Jahovic, N, Sener G, Cevik H, Ersoy Y, Arbak S, Yeğen BC. Amelioration of methotrexate–induced enteritis by melatonin in rats. Cell Biochem. Funct. [Internet]. 2004; 22(3):169–78. doi: https://doi.org/fc489q

Sener G, Eksioglu–Demiralp E, Cetiner M, Ercan F, Yeğen BÇ. Beta–glucan ameliorates methotrexate–induced oxidative organ injury via its antioxidant and immunomodulatory effects. Europ.J. Pharmacol. [Internet]. 2006; 542(1–3):170–178. doi: https://doi.org/d2zbgf

Serati–Nouri H, Azarmi YA, Movahedin M. Effect of growth hormone on testicular dysfunction induced by methotrexate in rats. Androl. [Internet]. 2009; 41:105–110. doi: https://doi.org/b9mg72

Güvenç M, Aksakal M. Ameliorating effect of kisspeptin‐10 on methotrexate‐induced sperm damages and testicular oxidative stress in rats. Androl. [Internet]. 2018; 50(8):e13057. doi: https://doi.org/gfbr6s

Padmanabhan S, Tripathi DN, Vikram A, Ramarao P, Jena GB. Cytotoxic and genotoxic effects of methotrexate in germ cells of male Swiss mice. Mutation Res./Genet. Toxicol. Environm. Mutagen. [Internet]. 2008; 655(1–2):59–67. doi: https://doi.org/ftt3c2

Johnson FE, Farr SA, Mawad M, Woo YCS. Testicular cytotoxicity of intravenous methotrexate in rats. J. Surgic. Oncol. [Internet]. 1994; 55:175–178. doi: https://doi.org/bqhvdh

Saxena AK, Dhungel S, Bhattacharya S, Jha CB, Srivastava AK. Effect of chronic low dose of methotrexate on cellular proliferation during spermatogenesis in rats. Arch. Androl. [Internet]. 2004; 50:33–35. doi: https://doi.org/fbkbqm

Palo AK, Choudhury RC. Modulation of methotrexateinduced cytogenotoxicity in mouse spermatogonia and its transmission in the male germline by caffeine. Environm. Toxicol. Pharmacol. [Internet]. 2006; 21:254–259. doi: https://doi.org/dv68bj

Öktem F, Yilmaz HR, Ozguner F, Olgar S, Ayata A, Uzar E, Uz E. Methotrexate–induced renal oxidative stress in rats: the role of a novel antioxidant caffeic acid phenethyl ester. Toxicol. Industr. Health. [Internet]. 2006; 22:241–247. doi: https://doi.org/cvzsdj

Belhan S, Özkaraca M, Kandemir FM, Gülyüz F, Yıldırım S, Ömür AD, Yener Z. Effectiveness of hesperidin on methotrexate–induced testicular toxicity in rats. Kafkas Üniversitesi Veteriner Fakültesi Dergisi. [Internet]. 2017; 23(5):789–796. doi: 10.9775/kvfd.2017.17752

Al–Yasiry ARM, Kiczorowska B. Frankincense–therapeutic properties. Postępy Higieny i Medycyny Doświadczalnej. [Internet]. 2016; 70:380–391. doi: https://doi.org/k4pg

Hussain H, Al–Harrasi A, Csuk R, Shamraiz U, Green IR, Ahmed I, Khan IA, Ali Z. Therapeutic potential of boswellic acids: a patent review (1990–2015). Expert Opinion on Therap. Patents. [Internet]. 2017; 27(1):81–90. doi: https://doi.org/k4ph

Sharma A, Upadhyay J, Jain A, Kharya MD, Namdeo A, Mahadik KR. Antioxidant activity of aqueous extract of Boswellia serrata. J. Chem. Bio. Phy. Sci. 2011; 1(1):60–71.

Singh P, Chacko KM, Aggarwal ML, Bhat B, Khandal RK, Sultana S, Kuruvilla BT. A–90 Day Gavage Safety Assessment of Boswellia serrata in rats. Toxicol. Intern. [Internet]. 2012; 19(3):273–278. doi: https://doi.org/k4pk

Arkali G, Aksakal M, Kaya ŞÖ. Protective effects of carvacrol against diabetes–induced reproductive damage in male rats: Modulation of Nrf2/HO–1 signalling pathway and inhibition of Nf–kB–mediated testicular apoptosis and inflammation. Androl. [Internet]. 2021; 53:e13899. doi: https://doi.org/k4pn

Lowry OH. Protein measurement with folin phenol reagent. J. Biol. Chem. 1951; 193:265–275.

Placer ZA, Cushman LL, Johnson BC. Estamination of product of lipid peroxidation (Malonlydialdehyde) in biochemical systems. Analyt. Biochem. [Internet]. 1966; 16:359–64. doi: https://doi.org/b96rpj

Sedlak J, Lindsay RH. Estimation of total protein bound and nonprotein sulfhydryl groups in tissue with Ellmann’s reagent. Analyt. Biochem. [Internet]. 1968; 25:192–205. doi: https://doi.org/csbsfm

Lawrence RA, Burk RF. Glutathione peroxidase activity in selenium–deficient rat liver. Biochem. Biophys. Res. Commun. [Internet]. 1976; 71:952–958. doi: https://doi.org/d3vv59

Türk G, Ateşşahin A, Sönmez M, Yüce A, Çeribaşı AO. Lycopene protects against cyclosporine A–induced testicular toxicity in rats. Theriogenol. [Internet]. 2007; 67:778–785. doi: https://doi.org/fxghnh

Sönmez M, Türk G, Yüce A. The effect of ascorbic acid supplementation on sperm quality, lipid peroxidation and testosterone levels of male Wistar rats. Theriogenol. [Internet]. 2005; 63(7):2063–2072. doi: https://doi.org/cn6kn5

Armagan A, Uzar E, Uz E, Yilmaz HR, Kutluhan S, Koyuncuoglu HR, Soyupek S, Cam H, Serel TA. Caffeic acid phenethyl ester modulates methotrexate–induced oxidative stress in testes of rat. Human Experim. Toxicol. [Internet]. 2008; 27 (7):547–552. doi: https://doi.org/c4drd3

Aldhahrani A, Soliman MM, Althobaiti F, Alkhedaide A, Nassan MA, Mohamed WA, Youssef GBA, Said AM. The modulatory impacts of Glycyrrhiza glabra extract against methotrexate–induced testicular dysfunction and oxidative stress. Toxicol. Res. [Internet]. 2021; 10 (4): 677–686. doi: https://doi.org/k4pr

Belhan S, Çomaklı S, Küçükler S, Gülyüz F, Yıldırım S, Yener Z. Effect of chrysin on methotrexate‐induced testicular damage in rats. Androl. [Internet]. 2019; 51:e13145. doi: https://doi.org/gmcjq8

Mansour DF, Saleh DO, Ahmed–Farid OA, Rady M, Bakeer RM, Hashad IM. Ginkgo biloba extract (EGb 761) mitigates methotrexate–induced testicular insult in rats: Targeting oxidative stress, energy deficit and spermatogenesis. Biomed Pharmacother. [Internet]. 2021; 143:112201. doi: https://doi.org/k4ps

Al–Yahy AA, Asad M, Sadaby A, Alhussaini MS. Repeat oral dose safety study of standardized methanolic extract of Boswellia sacra oleo gum resin in rats. Saudi J. Biol. Sci. [Internet]. 2020; 27:117–123. doi: https://doi.org/k4pt

Sami MM, Ali EA, Galhom RA, Youssef AM, Mohammad HM. Boswellic acids ameliorate doxorubicin–induced nephrotoxicity in mice: A focus on antioxidant and antiapoptotic effects. Egyptian J. Basic Appl. Sci. [Internet]. 2019; 6:10–24. doi: https://doi.org/dhvvg8

Nusier MK, Bataineh HN, Bataineh ZM, Daradka HM. Effect of frankincense (Boswellia thurifera) on reproductive system in adult male rat. J. Health Sci. [Internet]. 2007; 53:365–370. doi: https://doi.org/k4pv

Padmanabhan S, Tripathi DN, Vikram A, Ramarao P, Jena GB. Methotrexateinduced cytotoxicity and genotoxicity in germ cells of mice: Intervention of folic and folinic acid. Mutation Res./Genet. Toxicol. Environm. Mutagenesis. [Internet]. 2009; 673:43–52. doi: https://doi.org/c23bc7

Armagan A, Uzar E, Uz E, Yilmaz HR, Kutluhan S, Koyuncuoglu HR, Soyupek S, Cam H, Serel TA. Caffeic acid phenethyl ester modulates methotrexate–induced oxidative stress in testes of rat. Human Experim. Toxicol. [Internet]. 2008; 27(7):547–552. doi: https://doi.org/c4drd3

Vardi N, Parlakpinar H, Ates B, Cetin A, Otlu A. Antiapoptotic and antioxidant effects of beta–carotene against methotrexate–induced testicular injury. Fertil. Steril. [Internet]. 2009; 92(6):2028–2033. doi: https://doi.org/b2n98v

Eid NAS, Shibata MA, Ito Y, Kusakabe K, Hammad H, Otsukı Y. Involvement of Fas system and active caspases in apoptotic signalling in testicular germ cells of ethanol–treated rats. Intern. J. Androl. [Internet]. 2002; 25(3):159–167. doi: https://doi.org/fq69t5

Sherif IO, Al–Mutabagan LA, Sarhan OM. Ginkgo biloba extract attenuates methotrexate–induced testicular ınjury in rats: Cross–talk between oxidative stress, inflammation, apoptosis, and miRNA–29a expression. Integrative Cancer Therap. [Internet]. 2020; 19:e–1534735420969814. doi: https://doi.org/k4pz

Yuluğ E, Türedi S, Alver A, Türedi S, Kahraman C. Effects of resveratrol on methotrexate–ınduced testicular damage in rats. The Scientif. World J. [Internet]. 2013; 2013:489659. doi: https://doi.org/gb7xk7

Doaee P, Rajaei Z, Roghani M, Alaei H, Kamalinejad M. Effects of Boswellia serrata resin extract on motor dysfunction and brain oxidative stress in an experimental model of Parkinson´s disease. Avicenna J. PhytoMed. 2019; 9(3):281–290.

Tohamy HG, El–kazaz SE, Alotaibi SS, İbrahiem HS, Shukry M, Mahmoud Dawood AO. Ameliorative effects of boswellic acid on fipronil–ınduced toxicity: Antioxidant state, apoptotic markers, and testicular steroidogenic expression in male rats. Anim. [Internet]. 2021; 11(5):1302. doi: https://doi.org/k4p5

Gupta M, Singh S, Kurmi A, Luqman S, Saikia D, Thomas M, Rout PK. Correlation of boswellic acids with antiproliferative, antioxidant and antimicrobial activities of topographically collected Boswellia serrata oleo–gum–resin. PhytoMed. [Internet]. 2022; 2:100289. doi: https://doi.org/k4p7

Yüncü M, Bükücü N, Bayat N, Sencar L, Tarakçıoğlu M. The effect of vitamin E and L–carnitine against methotrexate–induced injury in rat testis. Turkish J. Med. Sci. [Internet]. 2015; 45:517–525. doi: https://doi.org/k4p8

Aslankoc R, Ozmen O, Ellidag HY. Ameliorating effects of agomelatine on testicular andepididymal damage induced by methotrexate in rats J Biochem. Molec. Toxicol. [Internet]. 2020; 34:e22445. doi: https://doi.org/k4qb

Publicado
2024-01-01
Cómo citar
1.
Arkalı G, Acısu TC, Badıllı N, Güler–Ekmen E, Tanyeri OS, Toz A, Çay M, Yüce A, Aksakal M. Efecto del extracto de Boswellia serrata sobre el daño testicular inducido por Metotrexato. Rev. Cient. FCV-LUZ [Internet]. 1 de enero de 2024 [citado 28 de abril de 2024];34(1):6. Disponible en: https://www.produccioncientificaluz.org/index.php/cientifica/article/view/41139
Sección
Medicina Veterinaria