Quantitative and qualitative analysis of neuroinflammation by beta amyloid 1-42 toxin after treatment with resveratrol-loaded nanoparticles

Autores/as

DOI:

https://doi.org/10.11606/issn.2176-7262.rmrp.2023.207173

Palabras clave:

Nanoparticles, Resveratrol, Alzheimer's

Resumen

Background: This study evaluated the effects of zein nanoparticles with resveratrol on neuroinflammation caused by Alzheimer’s disease. Method: The sample consisted of 30 animals divided into control (C), positive control (CP), white nanoparticles (NB), resveratrol nanoparticles (NR) and resveratrol (R) groups. The animals received 10 mg/kg of resveratrol or nanoparticles according to the group, daily, for 15 days, oral administration. Afterward, they were
submitted to immunohistochemical (IHC) analyses. Results: the IHC showed that there was no change in the morphological brain composition in the NR and C groups. Conversely, in the CP, NB, and R groups, changes in the deposition of Anti Tau were observed. The NR group showed a normal projection of taurine in the axon, which was not presented in the same way in the other groups. The CD68 marker showed no microglial activation in the R and C groups. Quantitative analyses of Anti Beta-Amyloid in the NR group showed a statistical difference compared
to the CP, NB, and R groups, whereas the Anti Tau analysis showed a significant difference between the CP and NR groups. The CD68 marker showed a significant difference between the C and NR groups. The analysis of cytokines showed a significant difference in TNF-α between the C and CP groups, C and NB groups, CP and NR groups, and NB and NR groups. IL-6 and InF-δ showed no significant difference between all groups. IL-10 showed significant differences between the C and NR groups, C and R groups, and CP and NR groups. Conclusion: NR prevented the evolution of neuroinflammation.

Descargas

Los datos de descarga aún no están disponibles.

Biografía del autor/a

  • Mariane Maria Silveira Vieira de Lima, Mid-West State University,(PR), Brazil

    Master by the Graduate Program in Nanosciences and Biosciences

  • Maria Elvira Ribeiro Cordeiro, Mid-West State University,(PR), Brazil

    Master’s Degree student in the Pharmaceutical Sciences Post Graduation

  • Flávio Klinpovous Kerppers, Mid-West State University,(PR), Brazil

    Pharmacist

  • Ketllin Bragnholo, Mid-West State University,(PR), Brazil

    Physiotherapist

  • Luiza Ferreira Cunha, Mid-West State University,(PR), Brazil

    Pharmacist

  • Maiara Fonseca, Mid-West State University, (PR), Brazil

    Physiotherapist

  • Tatiane Budniak Mazur, Mid-West State University, (PR), Brazil

    Physiotherapist

  • Christiane Schineider Machado, Mid-West State University, (PR), Brazil

    Researcher at the Pharmaceutical Nanotechnology Laboratory

  • Rubiana Mara Mainardes, Mid-West State University, (PR), Brazil

    Professor of the Pharmacy course

  • Afonso Shiguemi Inoue Salgado, Mid-West State University, (PR), Brazil

    Physiotherapist and Nutritionist

  • André Alexandre Pezzini, State University of West Paraná, Cascavel, (PR), Brazil.

    Professor of the Dentistry Course

  • Ana Carolina Dorigoni Bini, Mid-West State University, (PR), Brazil

    Professor of the Physiotherapy course

  • Ivo Ilvan Kerppers, Mid-West State University, (PR), Brazil

    Professor of the Physiotherapy course

Referencias

Pandey G, Ramakrishnan V. Invasive and non-invasive therapies for Alzheimer’s disease and other amyloidosis Biophys. Rev. 2020; 12:1175–1186. https://doi.org/10.1007/s12551-020-00752-y

Falco A, Cukierman DS, Hauser-Davis RA e Rey NA. Doença De Alzheimer: Hipóteses Etiológicas E Perspectivas De Tratamento. Quim. Nova. 2016; 39(1): 63-80.

Shengquan H, Yanfang X, Yubo F, Shinghung M, Jiajun W, Jing T,Yuanping P, Rongbiao P, Karl WT, Fufeng L, Zhixiu L,Yifan H. Significant combination of Aβ aggregation inhibitory and neuroprotectivepropertiesinsilico, in vitro and in vivo by bis(propyl)-cognitin, amultifunctional anti-Alzheimer’sagent. European J. of Pharmacol. 2020; 876, 1-10.

Sawda, C, Moussa, C, Turner, RS. Resveratrol for Alzheimer’sdisease. Anais da Academia de Ciências de Nova York. 2017; 1403(1):142-149.

Silva LR, Vianna CMM, Mosegui GBG, Peregrino AAF, Marinho V, Laks J. Cost-effectiveness analysis of the treatment of mild and moderate Alzheimer’s disease in Brazil. Braz. J. Psychiatr. 2019. 41(3): 218–224.

Ministério da Saúde. Protocolo Clínico e Diretrizes Terapêuticas- Doença de Alzheimer. PORTARIA CONJUNTA Nº 13. 2017.

Piovesana MCFS, Garcia FR, Carrasco KG, Tognola WA. Reassessment of the dementia diagnosis of Alzheimer’s disease in patients enrolled on the cholinesterase inhibitors dispensation program. Dement. Neuropsychol. 2012; 6 (4): 270–275.

Cheng, G., Xu P, Zhang M, Chen J, Sheng R, Ma Y. Resveratrol-maltol hybrids as multi-target-directed agents for Alzheimer’s disease. Bioorganic & Med. Chem. 2018; 26(22):5759-5765.

Jeřábek J, Uliassi E, Guidotti L, Korabecny J, Soukup O, Sepsova V, Hrabinova M, Kuca K, Bartolini M ,Peña Altamira MA, Petralla S, Monti B, Roberti M, Bolognesi M L. Tacrine-resveratrol fused hybrids as multi-target-directed ligands against Alzheimer's disease, European J. of Med. Chem. 2017; 127:250-262. https://doi.org/10.1016/j.ejmech.2016.12.048

Zhong Q, Jim M. Zein nanoparticles produced by liquid-liquid dispersion. Food Hydrocoll. 2009; 23 (8): 2380–2387.

Pauluk D, Padilha AK, Khalil NM, Rubiana MM. Chitosan-coated zein nanoparticles for oral delivery of resveratrol: Formation, characterization, stability, mucoadhesive properties and antioxidant activity. Food Hydrocoll. 2019; 94:411-417.

Panis LI, Geus BD, Vandenbulcke G, Willems H, Degraeuwe B, Bleux N, Mishra V, Thomas I, Meeusen R. Exposure to particulate matter in traffic: A comparison of cyclists and car passengers. Atmospheric Environment. 2010; 44(10):2263-2270.

Chatterjee A, Zakian S, Hu X, Singleton MR. Structural insights into the regulation of cohesion establishment by Wpl1. The EMBO J. 2013; 32(5):677-687.

Marcato PD. Preparação, caracterização e aplicações em fármacos e cosméticos de nanopartículas lipídicas sólidas. Revista Eletrônica de Farmácia. 2009; 6(2):1-37.

Maraicar KSH, Thirumoorthy N. Design and characterization of solid lipid nanoparticles by solvent evaporation method followed by homogenization. Int. J. of Biopharm. 2014; 014 5(3): 190-196.

Jawahar N, Meyyanathan SN, Reddy G, Sood S. Solid lipid nanoparticles for oraldelivery of poorly soluble drugs. J. of Pharm. Sci. & Res. 2012; 4(7):1848-1855.

Surender V, Deepika M. Solid lipid nanoparticles: a comprehensive review. J. of Chem. and Pharm. Res. 2016; 8(8):102-114.

Beckes DS, Zamberlan C, Colomé J, Souza MT, Marchiori MT, Erdann AL, Salazar-Maya AM. Interatividade sistêmica entre os conceitos interdependentes de cuidado de enfermagem. Aquichan. 2016; 16 (1):23-31.

Ilha S, Santos SSC, Backes DS, Barros EJL, Pelzer MT, Gautério-Abreu DP. Gerontotecnologias utilizadas pelos familiares/ cuidadores de idosos com Alzheimer: contribuição ao cuidado complexo. Texto Contexto Enfermagem. 2018; 27(4):1=16. https://doi.org/10.1590/0104-07072018005210017

Silva TU, Freitas LV, Rey NA, Machado SP. Estudo Teórico de potenciais agentes para o tratamento da doença de Alzheimer derivados da 8- Hidroxiquinolina com substituintes do tipo N-ACIL—hidrazona. Quim. Nova. 2018; 41(10):1132-1139.

Capiralla H, Vingtdeux V, Zhao H, Sankowski R, Al-Abed Y, Davies P, Marambaud P. Resveratrol mitigates lipopolysaccharide- and A-mediated microglial inflammation by inhibiting the TLR4/NF-kappaB/STAT signaling cascade. J. Neurochem. 2012; 120:461–472.

Hambardzumyan D, Gutimann DH, Kettenman H. The role of microglia and macrophages in glioma maintenace and progression. Nat. Neuroscien. 2015; 19(1):20.

Mehrabadi S, Sadr SS. Assessment of Probiotics Mixture on Memory Function,

Inflammation Markers, and Oxidative Stress in an Alzheimer's Disease Model of Rats.

Iran Biomed. J. 2020; 24(4):220-228. doi:10.29252/ibj.24.4.220

Salem HF, Khaershoum MR, Abou-Taleb HA, Naguig DM. Brain targeting of resveratrol through intranasal lipid vesicles labelled with gold nanoparticles:in vivo evaluation and bioaccumulation investigation using computed tomography and histopathological examination. J. of Drug Targeting. 2019; 27(10):1127-1134.

Descargas

Publicado

— Actualizado el 2023-12-18

Número

Sección

Artigo Original

Cómo citar

1.
Lima MMSV de, Cordeiro MER, Kerppers FK, Bragnholo K, Cunha LF, Fonseca M, et al. Quantitative and qualitative analysis of neuroinflammation by beta amyloid 1-42 toxin after treatment with resveratrol-loaded nanoparticles. Medicina (Ribeirão Preto) [Internet]. 2023 Dec. 18 [cited 2024 May 11];56(4):e-207173. Available from: https://www.revistas.usp.br/rmrp/article/view/207173