Illustration of the experimental design.

<p>Arrows with asterisk indicate an evaluation of the motor behavior, which included gait analysis, rotarod performance and ambulatory activity in the open field. Double asterisks indicate EMG recordings. Rats were 12 months old at the beginning of the experiment.</p

BDNF gene transfection by NTS-polyplex to dopamine neurons of substantia nigra pars compacta.

<p>(A) Panoramic view of the labeled TH+ neurons. (B) Amplification of the zone indicated by the frame in A. The arrowheads show the co-localization of the BDNF-flag in the TH+ neurons. This is a representative illustration of the BDNF-flag expression.</p

The combined treatment restored the TH immunoreactivity of the striatum.

<p>(A) Representative micrographs of TH immunoreactivity showing that the lesion extends along the rostro-caudal extention of the striatum. (B). Representative micrographs showing the effect of the treatments on TH immunoreactivity of the striatum. The black arrows show lesion produced by 6-OHDA. (C) Optical densitometry analysis of TH-immunoreactivity in dorso-medial (DMS), dorso-lateral (DLS) and ventral (VS) regions of the striatum. The recovery produced by the treatments was significant (DMS: F_{2, 9} = 9.694, <i>P</i> < 0.0057; DLS: F_{2, 9} = 40.46, <i>P</i> < 0.0001 and VS; F_{2, 9} = 19.93, <i>P</i> < 0.0005, One-way ANOVA) * <i>P</i> < 0.05; ** <i>P</i> < 0.01; *** <i>P</i> < 0.001 compared with saline-treated rats; ^& <i>P</i> < 0.01 compared with the 7-OH-DPAT alone (Bonferroni’s Multiple Comparison Post tests). The data are given as the mean ± SEM (<i>n</i> = 5 rats per group). The insert shows the three different sectors where the OD was determined.</p

Administration of the D3 agonist associated with the BDNF transfection restored motor coordination.

<p>The lesion reduced the time on the rod (A-I) and the rotarod performance (B). The combined treatment normalized the time on the rod (A-II) and the rotarod performance (B). The effect persisted two months after the treatment (A-III and B). The D3 agonist alone also recovered the motor coordination (A, B) but the rats dragged the contralateral hind limb during rod rotation (arrows in C and supplementary videos <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0117391#pone.0117391.s003" target="_blank">S3 Video</a>—ROTAROD PERFORMANCE IN NORMAL SPEED and <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0117391#pone.0117391.s004" target="_blank">S4 Video</a>- ROTAROD PERFORMANCE IN SLOW MOTION). Saline-treated rats did not recover the rotarod performance (A, B). The recovery produced by the treatments were significant (AI: F_{3, 12} = 9.881, <i>P</i> < 0.0015; AII: F_{3, 12} = 8.879, <i>P</i> < 0.0023; AIII: F_{3, 12} = 12.49, <i>P</i> < 0.0005 and B: F_{3, 15} = 21.84, <i>P</i> < 0.0001, One-way repeated-measures ANOVA). * <i>P</i> < 0.05; ** <i>P</i> < 0.01; *** <i>P</i> < 0.001 compared with saline-treated rats. ^# <i>P</i> = No significant difference compared with intact rats (Bonferroni’s Multiple Comparison Post tests). The data are given as the mean ± SEM (<i>n</i> = 5–6 rats per group). C illustrates representative cases.</p

The combined treatment recovered the nigro-striatal innervation.

<p>(A) Representative micrographs of the substantia nigra pars compacta showing TH+ neurons with the presence of rhodamine-labeled dextran amine (arrowheads), previously injected into the striatum. (B) Graph showing the percentage of rhodamine-labeled TH+ neurons with respect to the total of TH+ neurons of the same substantia nigra pars compacta, in each experimental condition. The recovery produced by the treatments was significant (F_{2, 8} = 18.34, <i>P</i> < 0.0010, One-way ANOVA). * <i>P</i> < 0.05; ** <i>P</i> < 0.01 compared with saline-treated rats (Bonferroni’s Multiple Comparison Post tests). The data are given as the mean ± SEM (<i>n</i> = 4 rats per group).</p

The combined treatment recovered normal muscle tone.

<p>The lesion increased the EMG activity of the contralateral gastrocnemius but did not affect the EMG of the ipsilateral one (A). The combined treatment normalized the EMG activity (A and B) and the effect persisted two months after the treatment (B). The D3 agonist also reduced the EMG, but the reduction was partial and occurred two months after the treatment (B). The recovery produced by the combined treatment was significant (F_{2, 6} = 5.674, <i>P</i> < 0.0414, One-way repeated-measures ANOVA). * <i>P</i> < 0.05; ** <i>P</i> < 0.01 compared with saline-treated rats (Bonferroni’s Multiple Comparison Post tests). The data are given as the mean ± SEM (<i>n</i> = 5 rats per group). A, shows a representative case.</p

The combined treatment did not recover the ambulatory activity and rearing in the open field.

<p>The lesion reduced the ambulatory activity evaluated by the distance traveled (A) and frequency of rearing (B) during the first ten min in the open field. However, it did not produce bradykinesia assessed by the speed of walking (C). None of the treatments recovered the ambulatory activity or rearing (A and B). Intact rats did not showed changes either in ambulation or in rearing, throughout the experiment. The 6-OHDA lesion reduced significantly the traveled distance and frequency of rearing (A: F_{3, 6} = 73.75, <i>P</i> < 0.0001 and B: F_{3, 6} = 57.30, <i>P</i> < 0.0001, One-way repeated-measures ANOVA) but it did not produce a significant effect on bradykinesia (C: F_{3, 6} = 3.563, <i>P</i> < 0.0868, One-way repeated-measures ANOVA). *** <i>P</i> < 0.001 compared with saline-treated rats. ^# <i>P</i> = No significant difference compared with saline-treated rats (Bonferroni’s Multiple Comparison Post tests). The data are given as the mean ± SEM (<i>n</i> = 5–6 rats per group).</p

The combined treatment restored gait.

<p>The lesion increased the angle of the contralateral ankle during the dorsiflexion of the swing phase of gait (arrows) and the undulatory displacement of the hip (limping), red line in A. The combined treatment normalized both conditions (A, B) and supplementary videos (<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0117391#pone.0117391.s001" target="_blank">S1 Video</a>—GAIT ANALYSIS IN NORMAL SPEED and <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0117391#pone.0117391.s002" target="_blank">S2 Video</a>—GAIT ANALYSIS IN SLOW MOTION). The D3 agonist alone did not restore neither the hip displacement (not shown) nor the angle of the ankle during gait. The increase in the angle produced by the lesion persisted all along the experiment (saline-treated rats) in B. The recovery produced by the combined treatment was significant (F_{3, 15} = 26.09, <i>P</i> < 0.0001, One-way repeated-measures ANOVA). *<i>P</i> < 0.05; ** <i>P</i> < 0.01; *** <i>P</i> < 0.001compared with saline-treated rats; ^# <i>P</i> = No significant difference compared with intact rats (Bonferroni’s Multiple Comparison Post tests). A, illustrate a representative case. The data are given as the mean ± SEM (<i>n</i> = 5–6 rats per group).</p

L'Auto-vélo : automobilisme, cyclisme, athlétisme, yachting, aérostation, escrime, hippisme / dir. Henri Desgranges

26 octobre 19201920/10/26 (A21,N7255)

NRTN gene transfection increase spine density and total number of intersections in MSN.

<p><b>A</b>. Sholl diagram for the morphological study of dendrites and dendritic spines. <b>B</b>. Representative micrograph of a medium spiny neuron (MSN) of a healthy striatum. The arrow shows the 50 μm segment (primary dendrite) where dendritic spines were analyzed. Upper calibration bar = 25 μm. The small panels show different types of spines (thin, mushroom, stubby and wide, from left to right) indicated by the arrow. Calibration bar = 5 μm. The transfections of pGreenLantern-1 (GFP) and pTracer-mNRTN-His (NRTN) plasmids were made at week 12 after lesion and the Sholl analysis was performed at the end of the study (12 weeks after transfection or 24 weeks after lesion). UT = untransfected rats with lesion. <b>C.</b> Sholl analysis of total number of intersections along dendritic trees in MSNs at all distances in 200-μm radius from the soma. <b>D.</b> Plot of mean spine density analyzed per 50-μm primary dendrite from cell body (proximal segment, upper arrow in <b>B</b>) from six neurons per rat. All values represent the mean ± SEM (<i>n</i> = 6 independent rats in each experimental condition). Statistical analysis (<b>C</b> and <b>D</b>) was performed using one-way ANOVA and Tukey <i>post-hoc</i> test.</p