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[Abstract Title]. - Society for Neuroscience

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picomolar affinity, neutralising its activity. Then, bladder function was monitored <strong>for</strong> 2 hours in<br />

anaesthetized rats, followed by perfusion-fixation. Spinal cord segments L6 were collected, postfixed<br />

and cryoprotected in sucrose. Segments were cut into 40 κm sections and immunoreacted<br />

against activated ERK and c-Fos.<br />

In CYP-injected rats treated with intravenous saline, the number of bladder contractions per<br />

minute was significantly increased in comparison with naïve rats (1.17±0.16 versus 0.60±0.08,<br />

respectively; p

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