El efecto protector de Aspalathus linearis contra la úlcera gástrica experimental inducida por etanol en ratas

  • İdris Oruç Dicle University, Faculty of Medicine, Department of Nephrology–Internal Medicine. Diyarbakır, Turkey
  • Zelal Karakoç Dicle University, Faculty of Veterinary Medicine, Department of Laboratory Animals. Diyarbakır, Turkey
  • Muzaffer Aydın Ketani Dicle University, Faculty of Veterinary Medicine, Histology&Embryology Department. Diyarbakır, Turkey
  • Filiz Akduman Beypazarı State Hospital, Pediatrics. Turkey
  • Nazan Baksi Dicle University, Faculty of Veterinary Medicine, Department of Laboratory Animals. Diyarbakır, Turkey
  • Veli Korkmaz Nusaybin State Hospital, Pediatrics. Turkey
  • Zeynep Oruç Dicle University, Faculty of Medicine, Department of Medical Oncology. Diyarbakır, Turkey
Palabras clave: Aspalathus linearis, CD8, CD68, molécula de clase MHC, gastritis

Resumen

Este estudio tuvo como objetivo investigar el efecto de Aspalathus linearis en la expresión de moléculas del complejo mayor de histocompatibilidad (MHC) que presentan antígenos a las células CD8, CD68 y T en un modelo experimental de gastritis en ratas (Rattus norvegicus). También tuvo como objetivo evaluar los cambios en los niveles de factor de necrosis tumoral alfa, mieloperoxidasa, superóxido dismutasa y malondialdehído desencadenados por las propiedades antioxidantes de la planta. En el estudio se utilizaron veinticuatro ratas albinas Wistar hembra. En un modelo de gastritis inducida por etanol, se administró A. linearis a los grupos de tratamiento por sonda oral durante 5 días. Se tomaron muestras de sangre y tejido estomacal para análisis. La evaluación bioquímica mostró que los niveles de TNF–α y mieloperoxidasa disminuyeron y la actividad de superóxido dismutasa aumentó en los grupos tratados con A. linearis en comparación con el grupo de etanol. La evaluación histoquímica reveló que la severidad de la inflamación disminuyó en las ratas con gastritis sometidas al A. linearis. También se detectó que disminuyó el número de células que mostraban expresión de CD8 y CD68. El número de células inmuno positivas MHC II fue mayor en el grupo tratado con A. linearis en comparación con el control y otros grupos de tratamiento. Se concluyó que A. linearis tiene un efecto protector sobre la mucosa gástrica al reducir la severidad del estrés oxidativo debido a sus propiedades antioxidantes, antiinflamatorias y anti apopitóticas.

Descargas

La descarga de datos todavía no está disponible.

Citas

Akcakavak G, Tuzcu M, Tuzcu N, Celik Z, Tural A, Dagar O. Investigation with Real–Time PCR and Histopathology on the presence of H. felis, H. heilmannii and H. pylori in dogs. Rev. Cientif. Fac. Cienc. Vet. [Internet]. 2023; 33(1):e–33214 .doi:10.52973/rcfcv–e33214.

Sipponen P, Maaroos HI. Chronic gastritis. Scand. J. Gastroenterol. [Internet]. 2015; 50(6):657–67. doi: https://doi.org/gmppwm

Rajendran P, Nandakumar N, Rengarajan T, Palaniswami R, Gnanadhas EN, Lakshminarasaiah U, Gopas J, Nishigaki I. Antioxidants and human diseases. Clin. Chim. Acta. [Internet]. 2014; 436:332–47. doi: https://doi.org/f6gtv6

Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Intern. J. Biochem. Cell. Biol. [Internet]. 2007; 39(1):44–84. doi: https://doi.org/bdqwsb

Lyras L, Cairns NJ, Jenner A, Jenner P, Halliwell B. An assessment of oxidative damage to proteins, lipids, and DNA in brain from patients with Alzheimer's disease. J. Neurochem. [Internet]. 1997; 68(5):2061–9. doi: https://doi.org/b76dxb

Sosa V, Moliné T, Somoza R, Paciucci R, Kondoh H, Lleonart ME. Oxidative stress and cancer: an overview. Ageing Res. Rev. [Internet]. 2013; 12(1):376–90. doi: https://doi.org/f4jsm8

Domnick A, Winter C, Sušac L, Hennecke L, Hensen M, Zitzmann N, Trowitzsch S, Thomas C, Tampé R. Molecular basis of MHC I quality control in the peptide loading complex. Nat. Commun. [Internet]. 2022; 13(1):4701. doi: https://doi.org/gqnpg5

Zhao C, Pang X, Yang Z, Wang S, Deng,H, Chen X. Nanomaterials targeting tumor associated macrophages for cancer immunotherapy. J.Contr. Release. [Internet]. 2022; 341:272–284. doi: https://doi.org/gphng9

Gilani AH, Khan AU, Ghayur MN, Ali SF, Herzig, JW. Antispasmodic effects of Rooibos tea (Aspalathus linearis) is mediated predominantly through K+ –channel activation. Basic Clin. Pharmacol. Toxicol. [Internet]. 2006; 99(5):365–73. doi: https://doi.org/ddkwdj

Obasa Z, Van–Vuuren M.A, Huisamen B, Windvogel S.L. The modulating effects of green rooibos (Aspalathus Linearis) extract on vascular function and antioxidant status in obese Wistar rats. Cardiovasc. J. Afr. [Internet]. 2021; 32(2):87–97. doi: https://doi.org/gnjjmz

Kang S, Kim CH, Jung H, Kim E, Song HT, Lee JE. Agmatine ameliorates type 2 diabetes induced–Alzheimer's disease–like alterations in high–fat diet–fed mice via reactivation of blunted insulin signalling. Neuropharmacol. [Internet]. 2017; 113(A):467–479. doi: https://doi.org/f9hh44

Diniz PB, Ribeiro AR, Estevam CS, Bani CC, Thomazzi SM. Possible mechanisms of action of Caesalpinia pyramidalis against ethanol–induced gastric damage. J. Ethnopharmacol. [Internet]. 2015; 168:79–86. doi: https://doi.org/f7ggzf

Mahmoud YL, Abd El–Ghffar, EA. Spirulina ameliorates aspirin–induced gastric ulcer in albino mice by alleviating oxidative stress and inflammation. Biomed. Pharmacother. [Internet]. 2019; 109:314–321. doi: https://doi.org/gjg7s2

Hong IS, Lee HY, Kim HP. Anti–oxidative effects of Rooibos tea (Aspalathus linearis) on immobilization–induced oxidative stress in rat brain. PLoS One. [Internet]. 2014; 9(1):e87061. doi: https://doi.org/gf4r4j

Saruhan BG, Topaloğlu u, Akbalık ME, Ketani MA, Sağsöz H. Distribution of Class II Major Histocompatibility Antigens in The Ductus Deferens of The Adult Bull and Ram. Dicle Üniv. Vet. Fak. Derg. 2016; 1(7):42–47.

Topaloğlu U, Karakoç Z, Akbalik ME, Saruhan B, Aydin N. Immunohistochemical Localization of Cytokeratin 8 in Testes of Different Cat Breeds. J. Dicle Univ. Fac. Vet. Med. [Internet]. 2022; 15(1):20–24. doi: https://doi.org/kqdp

Laine L, Weinstein WM. Histology of alcoholic hemorrhagic "gastritis": a prospective evaluation. Gastroenterol. [Internet]. 1988; 94(6):1254–62. doi: https://doi.org/gnqcpd

Guslandi M. Effects of ethanol on the gastric mucosa. Dig. Dis. [Internet]. 1987; 5(1):21–32. doi: https://doi.org/ds6wv3

Ko JK, Cho CH, Lam, SK. Adaptive cytoprotection through modulation of nitric oxide in ethanol–evoked gastritis. World J. Gastroenterol. [Internet]. 2004; 10(17):2503–8. doi: https://doi.org/kqdq

Yagi K. Lipid peroxides and human diseases. Chem. Phys. Lipids. [Internet]. 1987; 45(2–4):337–51. doi: https://doi.org/dp57vm

Halliwell B, Gutteridge JM. Oxygen free radicals and iron in relation to biology and medicine: some problems and concepts. Arch. Biochem. Biophys. [Internet]. 1986; 246(2):501–14. doi: https://doi.org/b3f9bc

Arthur JR. The glutathione peroxidases. Cell Mol. Life Sci. [Internet]. 2000; 57(13–14):1825–35. doi: https://doi.org/fsb4s8

Colarusso L, Serafini M, Lagerros YT, Nyren O, La Vecchia C, Rossi M, Ye W, Tavani A, Adami HO, Grotta A, Bellocco R. Dietary antioxidant capacity and risk for stroke in a prospective cohort study of Swedish men and women. Nutr. [Internet]. 2017; 33:234–239. doi: https://doi.org/f3t73h

Sánchez–Rodríguez MA, Mendoza–Núñez VM. Oxidative Stress Indexes for Diagnosis of Health or Disease in Humans. Oxid. Med. Cell Longev. [Internet]. 2019; 2019:4128152. doi: https://doi.org/kqdx

Longo B, Sommerfeld EP, Dos Santos AC, Da Silva R, Somensi LB, Mariano LNB, Boeing T, Faloni De A. S, De Souza P, Da Silva LM. Dual role of eugenol on chronic gastric ulcer in rats: Low–dose healing efficacy and the worsening gastric lesion in high doses. Chem. Biol. Interact. [Internet]. 2021; 333:109335. doi: https://doi.org/kqdz

Hendricks R, Pool EJ. The in vitro effects of Rooibos and Black tea on immune pathways. J. Immunoassay. Immunochem. [Internet]. 2010; 31(2):169–80. doi: https://doi.org/dvg7n3

Waisundara VY, Hoon, LY. Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer. J. Tradit. Complement. Med. [Internet]. 2015; 5(3):174–8. doi: https://doi.org/gnjjmt

Ulicná O, Vancová O, Bozek P, Cársky J, Sebeková K, Boor P, Nakano M, Greksák M. Rooibos tea (Aspalathus linearis) partially prevents oxidative stress in streptozotocin–induced diabetic rats. Physiol. Res. [Internet]. 2006; 55(2):157–164. doi: https://doi.org/kqd3

Lawal AO, Oluyede DM, Adebimpe MO, Olumegbon LT, Awolaja OO, Elekofehinti OO, Crown OO. The cardiovascular protective effects of rooibos (Aspalathus linearis) extract on diesel exhaust particles induced inflammation and oxidative stress involve NF–κB– and Nrf2–dependent pathways modulation. Heliyon. [Internet]. 2019; 5(3):e01426. doi: https://doi.org/kqd4

Baba H, Ohtsuka Y, Haruna H, Lee T, Nagata S, Maeda M, Yamashiro Y, Shimizu T. Studies of anti–inflammatory effects of Rooibos tea in rats. Pediatr. Intern. [Internet]. 2009; 51(5):700–4. doi: https://doi.org/dmkm6c

Karakus B, Odabasoglu F, Cakir A, Halici Z, Bayir Y, Halici M, Aslan A, Suleyman H. The effects of methanol extract of Lobaria pulmonaria, a lichen species, on indometacin–induced gastric mucosal damage, oxidative stress and neutrophil infiltration. Phytother. Res. [Internet]. 2009; 23(5):635–9. doi: https://doi.org/b5p9t2

Ahluwalia B, Magnusson MK, Öhman L. Mucosal immune system of the gastrointestinal tract: maintaining balance between the good and the bad. Scand. J. Gastroenterol. [Internet]. 2017; 52(11):1185–1193. doi: https://doi.org/gcpsf5

Dukhinova MS, Prilepskii AY, Shtil AA, Vinogradov VV. Metal Oxide Nanoparticles in Therapeutic Regulation of Macrophage Functions. Nanomaterials. 2019; 9(11):1631. doi: https://doi.org/gpr2rx

Akbalik ME, Erdoğan S, Saruhan BG, Sağsöz H. The distribution of immune system cells in bursa of Fabricius of partridge (Alectoris chukar). Eurasian J. Vet. Sci. [Internet]. 2019; 33(2):68–72 doi: https://doi.org/kqd5

Yalçin B. Major histocompatibility complex (MHC) molecules: their common characteristics and relations with diseases. Türkderm. [Internet]. 2013; 47(1):12–17. doi: https://doi.org/kqd6

Jurewicz MM, Stern LJ. Class II MHC antigen processing in immune tolerance and inflammation. Immunogenet. [Internet]. 2019; 71(3):171–187. doi: https://doi.org/gfkhrn

Publicado
2023-08-25
Cómo citar
1.
Oruç İdris, Karakoç Z, Ketani MA, Akduman F, Baksi N, Korkmaz V, Oruç Z. El efecto protector de Aspalathus linearis contra la úlcera gástrica experimental inducida por etanol en ratas. Rev. Cient. FCV-LUZ [Internet]. 25 de agosto de 2023 [citado 10 de mayo de 2024];33(2):7. Disponible en: https://www.produccioncientificaluz.org/index.php/cientifica/article/view/40746
Sección
Medicina Veterinaria