Anti-aging effects of guanosine in glial cells

被引:28
作者
Souza, Debora Guerini [1 ]
Bellaver, Bruna [1 ]
Bobermin, Larissa Daniele [1 ]
Souza, Diogo Onofre [1 ,2 ]
Quincozes-Santos, Andre [1 ,2 ]
机构
[1] Univ Fed Rio Grande do Sul, Inst Cincias Basicas Saude, Programa Posgrad Ciencias Biol Bioquim, Rio Grande Do Sul, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Inst Cincias Basicas Saude, Dept Bioquim, Rio Grande Do Sul, RS, Brazil
关键词
Aging; Adult/aged astrocytes; Guanosine; Heme oxygenase 1; ABSENCE EPILEPTIC ACTIVITY; NF-KAPPA-B; OXIDATIVE STRESS; HEME OXYGENASE-1; NEURODEGENERATIVE DISEASES; GLUTAMATE TRANSPORTERS; ADMINISTERED GUANOSINE; ASTROCYTE CULTURES; FREE-RADICALS; IN-VITRO;
D O I
10.1007/s11302-016-9533-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Guanosine, a guanine-based purine, has been shown to exert beneficial roles in in vitro and in vivo injury models of neural cells. Guanosine is released from astrocytes and modulates important astroglial functions, including glutamatergic metabolism, antioxidant, and anti-inflammatory activities. Astrocytes are crucial for regulating the neurotransmitter system and synaptic information processes, ionic homeostasis, energy metabolism, antioxidant defenses, and the inflammatory response. Aging is a natural process that induces numerous changes in the astrocyte functionality. Thus, the search for molecules able to reduce the glial dysfunction associated with aging may represent an approach for avoiding the onset of age-related neurological diseases. Hence, the aim of this study was to evaluate the anti-aging effects of guanosine, using primary astrocyte cultures from newborn, adult, and aged Wistar rats. Concomitantly, we evaluated the role of heme oxygenase 1 (HO-1) in guanosine-mediated glioprotection. We observed age-dependent changes in glutamate uptake, glutamine synthetase (GS) activity, the glutathione (GSH) system, pro-inflammatory cytokine (tumor necrosis factor alpha (TNF-alpha) and interleukin 1 beta (IL-1 beta)) release, and the transcriptional activity of nuclear factor kB (NFkB), which were prevented by guanosine in an HO-1-dependent manner. Our findings suggest guanosine to be a promising therapeutic agent able to provide glioprotection during the aging process. Thus, this study contributes to the understanding of the cellular and molecular mechanisms of guanosine in the aging process.
引用
收藏
页码:697 / 706
页数:10
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