Racz Boglarka, Horvath Gabriella, Reglodi Dora, Gasz Balazs, Kiss Peter, Gallyas Ferenc, Sumegi Balazs, Toth Gabor, Nemeth Adrienne, Lubics Andrea, Tamas Andrea
Department of Biochemistry and Medical Chemistry, University of Pecs, Hungary.
Regul Pept. 2010 Feb 25;160(1-3):91-8. doi: 10.1016/j.regpep.2009.12.003. Epub 2009 Dec 4.
Pituitary adenylate cyclase activating polypeptide (PACAP) is a pleiotropic and multifunctional neuropeptide. Numerous studies prove that PACAP has neuroprotective effects in diverse neuronal systems in vitro and in vivo. The involvement of PACAP in visual and olfactory sensory processing has also been documented, but little is known about its effects in the auditory system. The presence of PACAP and its receptor, the specific PAC1 receptor, has been shown in the cochlea and in brain structures involved in auditory pathways. The aim of the present study was to investigate whether PACAP is protective in cochlear oxidative stress-induced cell death, which is known to play a role in several ototoxic insults. Chicken cochlear cells were exposed to 1mM H(2)O(2), which resulted in a marked reduction of cell viability and a parallel increase of apoptotic and necrotic cells assessed by MTT test, annexin V/propidium iodide flow cytometry and JC-1 apoptosis assay. Co-incubation with 100nM PACAP increased cell viability and reduced the percentage of apoptotic cells. Furthermore, oxidative stress increased the activation of caspase-3, while simultaneous PACAP treatment reduced it. In summary, our present results demonstrate that PACAP effectively protects cochlear cells against oxidative stress-induced apoptotic cell death.
垂体腺苷酸环化酶激活多肽(PACAP)是一种具有多效性和多功能的神经肽。大量研究证明,PACAP在体外和体内的多种神经元系统中具有神经保护作用。PACAP参与视觉和嗅觉感觉处理也有文献记载,但对其在听觉系统中的作用知之甚少。PACAP及其受体(特异性PAC1受体)已在耳蜗和参与听觉通路的脑结构中被发现。本研究的目的是调查PACAP对耳蜗氧化应激诱导的细胞死亡是否具有保护作用,已知这种细胞死亡在几种耳毒性损伤中起作用。鸡耳蜗细胞暴露于1mM H₂O₂,通过MTT试验、膜联蛋白V/碘化丙啶流式细胞术和JC-1凋亡试验评估,这导致细胞活力显著降低,凋亡和坏死细胞平行增加。与100nM PACAP共同孵育可提高细胞活力并降低凋亡细胞百分比。此外,氧化应激增加了caspase-3的激活,而同时进行PACAP处理则降低了这种激活。总之,我们目前的结果表明,PACAP能有效保护耳蜗细胞免受氧化应激诱导的凋亡性细胞死亡。