Systemic Injection of Kainic Acid Differently Affects LTP Magnitude Depending on its Epileptogenic Efficiency
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Abstract
Seizures have profound impact on synaptic function and plasticity. While kainic acid is a popular method to induce seizures
and to potentially affect synaptic plasticity, it can also produce physiological-like oscillations and trigger some forms of
long-term potentiation (LTP). Here, we examine whether induction of LTP is altered in hippocampal slices prepared from
rats with different sensitivity to develop status epilepticus (SE) by systemic injection of kainic acid. Rats were treated with
multiple low doses of kainic acid (5 mg/kg; i.p.) to develop SE in a majority of animals (72–85% rats). A group of rats were
resistant to develop SE (15–28%) after several accumulated doses. Animals were subsequently tested using chronic
recordings and object recognition tasks before brain slices were prepared for histological studies and to examine basic
features of hippocampal synaptic function and plasticity, including input/output curves, paired-pulse facilitation and thetaburst
induced LTP. Consistent with previous reports in kindling and pilocapine models, LTP was reduced in rats that
developed SE after kainic acid injection. These animals exhibited signs of hippocampal sclerosis and developed
spontaneous seizures. In contrast, resistant rats did not become epileptic and had no signs of cell loss and mossy fiber
sprouting. In slices from resistant rats, theta-burst stimulation induced LTP of higher magnitude when compared with
control and epileptic rats. Variations on LTP magnitude correlate with animals’ performance in a hippocampal-dependent
spatial memory task. Our results suggest dissociable long-term effects of treatment with kainic acid on synaptic function
and plasticity depending on its epileptogenic efficiency.
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Suárez, L. M., Cid, E., Gal-Igesias, B., Inostroza, M., Brotons-Mas, J., Gómez-Domínguez, D., ..., & Solís, J. M. (2012). Systemic injection of kainic acid differently affects LTP magnitude depending on its epileptogenic efficiency. PloS One, 7(10), e48128.







