Vafaee Farzaneh, Zarifkar Asadollah, Emamghoreishi Masoumeh, Namavar Mohammad Reza, Shahpari Marzieh, Zarifkar Amir Hossein
Department of Neuroscience, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.
Department of Physiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Galen Med J. 2018 Nov 19;7:e1353. doi: 10.22086/gmj.v0i0.1353. eCollection 2018.
Insulin-like growth factor 2 (IGF-2) is a growth factor and an anti-inflammatory cytokine that plays a pivotal role in memory. In this study, we examined the effect of recombinant IGF-2 on memory impairment due to intracerebral hemorrhage (ICH). Avoidance and recognition memory, locomotor activity, neurological deficit score (NDS), and the level of the IGF-2 gene expression were evaluated.
To induce ICH, 100 μL of autologous blood was injected into the left hippocampus of male Sprague Dawley rats. Recombinant IGF-2 was injected into the damaged hippocampus 30 minutes after the induction of ICH. Then, over two weeks, NDS, locomotor activity, passive avoidance, and novel object recognition (NOR) test were evaluated. Finally, the level of IGF-2 gene expression was evaluated by using the real-time polymerase chain reaction technique.
Our results indicated that recombinant IGF-2 injection significantly increased step-through latency (P<0.001) and total time spent in the dark box (P<0.01). However, no significant difference was seen in recognition memory and NDS. Locomotor activity did not significantly change in any group. A significantly reduced level of IGF-2 was observed after two weeks (P<0.05).
The results of this study show that a single dose of recombinant IGF-2 injection can influence hippocampus-dependent memories. Importantly, IGF-2 did not change locomotor activity and NDS after two weeks, which probably represents its specific function in memory.
胰岛素样生长因子2(IGF-2)是一种生长因子和抗炎细胞因子,在记忆中起关键作用。在本研究中,我们检测了重组IGF-2对脑出血(ICH)所致记忆障碍的影响。评估了回避和识别记忆、运动活动、神经功能缺损评分(NDS)以及IGF-2基因表达水平。
为诱导脑出血,将100μL自体血注入雄性Sprague Dawley大鼠的左侧海马。在脑出血诱导后30分钟,将重组IGF-2注入受损海马。然后,在两周时间内,评估NDS、运动活动、被动回避和新物体识别(NOR)试验。最后,使用实时聚合酶链反应技术评估IGF-2基因表达水平。
我们的结果表明,注射重组IGF-2显著增加了穿梭潜伏期(P<0.001)和在暗箱中花费的总时间(P<0.01)。然而,在识别记忆和NDS方面未观察到显著差异。任何组的运动活动均无显著变化。两周后观察到IGF-2水平显著降低(P<0.05)。
本研究结果表明,单次注射重组IGF-2可影响海马依赖性记忆。重要的是,两周后IGF-2并未改变运动活动和NDS,这可能代表了其在记忆中的特定功能。