Axonal Branching and Recovery of Coordinated Muscle Activity by Prof. Dr. Doychin N. Angelov, Prof. Dr. Wolfram F. Neiss, PDF

By Prof. Dr. Doychin N. Angelov, Prof. Dr. Wolfram F. Neiss, Dr. Orlando Guntinas-Lichius, Prof. Dr. Michael Streppel, Dr. Konstantin Wewetzer (auth.)

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Additional info for Axonal Branching and Recovery of Coordinated Muscle Activity after Transection of the Facial Nerve in Adult Rats

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5 mA). 09 ms; (n=5). However, both latency and threshold values were dependent on slight differences in electrode position, and were thus disregarded for statistical analysis. The CMAP consisted of a fast 3-phasic positive-negative-positive wave, followed by a slow and not so prominent negative wave (Fig. 12A). With the recording procedure used here, the faster negative wave reflected the overlapping depolarizations of all innervated muscle fibers. 14 ms; n=5 rats) of the negative wave was due to the similar conductance velocities and excitability of the involved fibers.

Reprinted from Tomov et al. , manuscript in preparation). , Englewood, CO, USA). The spatial model consisted of three reference points (Fig. 5): 1. A point in the medial sagittal line Fr-Occ (perpendicular to a line connecting both orbits) close to the end of the nose. We selected this reference point because the permanent sniffing movements of the nose tip would jeopardize the measurements. 2. A point corresponding to the medial angle of the left (s) orbit. 3. A point corresponding to the medial angle of the right (r) orbit.

Subgroup F2 consisted of 24 blind adult female Sprague-Dawley (SD) rats (substrain Royal College of Surgeons, RCS). The RCS rats lose their photoreceptor cells 2 weeks after birth due to a genetic defect of the retinal pigment epithelium (Sheedlo et al. 1991; D’Cruz et al. 2000;). Thus, the mystacial vibrissae are the only available means for these animals to receive and resolve spatial information (Brecht et al. 1997). 28 Materials and Methods: Experimental Sets These animals were used in three experimental sets.

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