Table 1.
Behavioral Parameter | Group | 2N Mean±SEM |
Ts65Dn Mean±SEM |
p Value * | Interpretation | Brain region involved ** With Reference(s) |
|
---|---|---|---|---|---|---|---|
Total Ambulatory Distance Moved in Activity Chamber (cm) |
Female | 2111±225 | 3862±594 | p<0.01 | Ts65Dn mice are hyperactive in a novel environment. |
Cerebellum, cerebral cortex, septum, striatum, thalamic reticular nucleus, spinal cord, hippocampus (Deacon et al., 2002; Viggiano, 2008) |
|
Male | No Treatment | 2264±151 | 3638±388 | p<0.05 | |||
Saline | 2287±253 | 3186±163 | ns for treatment | Xamoterol has no effect on the activity of the mice. |
|||
Xam | 2554±192 | 3878±765 | |||||
Total Vertical Count in Activity Chamber (n) |
Female | 68.9±13.8 | 145.2±27.8 | p<0.01 | Ts65Dn mice rear and jump more than 2N mice in a novel environment |
||
Male | 75.0±6.1 | 147.7±7.3 | p<0.01 | ||||
Baseline Distance Moved in Each Hour in Home Cage(cm) |
Female | Dark | 2031±508 | 4122±789 | p<0.05 | Ts65Dn mice are hyperactive in their home cage environment. |
Hippocampus, prefrontal cortex. striatum, cerebral cortex, cerebellum, brain stem, spinal cord (Takakusaki, 2008) |
Light | 532±100 | 908±205 | ns | ||||
Male | Dark | 1088±196 | 2358±350 | p<0.01 | |||
Light | 366±27 | 511±96 | ns | ||||
Distance Moved in the Running Wheel in Home Cage (cm) |
Female | Dark | 27663±8845 | 39204±7842 | ns | Ts65Dn mice are hyperactive in the running wheel in their home cage environment. |
|
Light | 2298±1207 | 1812±971 | ns | ||||
Male | Dark | 16711±6912 | 43645±8032 | p<0.05 | |||
Light | 634±211 | 1762±750 | ns | ||||
Baseline Velocity in the Home Cage (cm/s) |
Female | Dark | 7.32±0.71 | 8.65±0.89 | ns | Ts65Dn mice move faster in their home cage environment. |
|
Light | 8.66±0.78 | 10.97±0.70 | p<0.05 | ||||
Male | Dark | 6.57±0.56 | 7.23±0.66 | ns | |||
Light | 7.87±0.37 | 11.07±1.02 | p<0.05 | ||||
Velocity in Running Wheel in Home Cage (cm/s) |
Female | Dark | 23.16±5.75 | 28.02±4.23 | ns | Ts65Dn mice run faster in the running wheel in their home cage environment. |
|
Light | 17.22±5.14 | 15.22±4.48 | ns | ||||
Male | Dark | 10.90±3.12 | 30.33±4.36 | p<0.01 | |||
Light | 4.15±0.55 | 11.80±2.48 | p<0.05 | ||||
Time in Shelter in Each Hour During the Baseline Recording in Home Cage (s) |
Female | Dark | 2653±107 | 1630±136 | p<0.01 | Ts65Dn mice spend less time in the shelter during the dark cycle. |
|
Light | 3238±42 | 3145±84 | ns | ||||
Male | Dark | 2536±182 | 1591±298 | p<0.01 | |||
Light | 3177±47 | 2752±331 | ns | ||||
Time in Shelter in Each Hour During the Running Wheel in Home Cage (s) |
Female | Dark | 1492±256 | 665±252 | p<0.05 | Ts65Dn mice spend less time in the shelter after adding the running wheel. |
|
Light | 3204±56 | 1568±579 | p<0.05 | ||||
Male | Dark | 2025±156 | 1440±144 | p<0.05 | |||
Light | 3189±63 | 3271±52 | ns | ||||
% of Spontaneous Alternation in T-maze |
Female | 65.0±3.3 | 48.5±3.7 | p<0.01 | Ts65Dn mice have impaired spatial working memory. |
Hippocampus (Devenport et al., 1988; Gerlai, 1998; Johnson et al., 1977) |
|
Male | No Treatment | 72.2±2.7 | 43.3±5.0 | p<0.001 | |||
Saline | 63.3±4.0 | 41.9±2.7 | p<0.01 | Xamoterol can rescue the deficit in spatial working memory, and betaxolol prevents this effect. |
|||
Xam | 64.4±2.1 | 60.4±4.5 | ns | ||||
Xam + Betax | 66.7±4.2 | 46.3±2.8 | p<0.01 | ||||
% of Correct Visit in Probe Trial after Place Learning in Intellicage |
Female | 60.3±2.7 | 66.2±4.0 | p=0.270 | Ts65Dn mice do not show a place learning deficit in a stress-free environment |
Hippocampus (Galsworthy et al., 2005) | |
% of Visits to Previously Punished Corner in Intellicage |
Female | 5.3±1.9 | 13.4±3.4 | p<0.05 | Ts65Dn mice show spatial learning deficit in a stressful environment. |
Hippocampus, amygdale (Galsworthy et al., 2005) |
|
Latency of First Satellite Box Entry in Intellicage (s) |
Female | 1172±175 | 587±75 | p<0.05 | Ts65Dn mice enter into the new compartment sooner. |
Hippocampus, amygdale (Galsworthy et al., 2005) |
|
Latency of First Satellite Box Entry in Intellicage (s) |
Female | 1172±175 | 587±75 | p<0.05 | Ts65Dn mice enter into the new compartment sooner. |
Hippocampus (Galsworthy et al., 2005) | |
Escape Latency in DMP (delayed matching-to-place ) Water Maze (s) |
Female | T3 | 50.97±6.80 | 76.42±3.16 | p<0.01 | Ts65Dn mice have a deficit in spatial working memory/episodic like-memory. |
Hippocampus (Steele and Morris, 1999) |
Male | T2 | 55.98±5.18 | 77.29±4.18 | p<0.05 | |||
T3 | 46.50±5.04 | 73.96±4.64 | p<0.001 | ||||
T4 | 38.59±5.50 | 70.44±5.86 | p<0.001 | ||||
% of Total Investigation in Novel Object Recognition |
Male | Saline | 59.0±5.5 | 44.9±3.3 | p<0.05 | Xamoterol can rescue the impairment of novel object recognition in Ts65Dn mice. |
Hippocampus, perirhinal cortex, raphe nuclei (Mumby et al.,2005; Winters et al., 2004; Lieben et al., 2006) |
Xam | 78.6±2.6 | 73.6±4.2 | ns | ||||
% Freezing in Tone-cued Fear Conditioning |
Female | 27.19±6.34 | 22.24±3.98 | ns | Ts65Dn do not have a deficit in tone-cued fear conditioning. |
Hippocampus, amygdale (Anagnostaras et al., 1999; Kim and Fanselow, 1992) |
|
Male | 31.06±3.84 | 21.73±2.89 | ns | ||||
% Freezing in Contextual Fear Conditioning |
Female | 16.37±5.30 | 4.65±1.66 | p<0.05 | Ts65Dn mice show a deficit in contextual fear conditioning. |
||
Male | No Treatment | 19.33±4.16 | 7.93±2.87 | p<0.05 | |||
Saline | 40.98±6.25 | 19.65±3.68 | p<0.01 | Xamoterol rescues the deficit in contextual fear conditioning, and betaxolol prevents this effect. |
|||
Xam | 38.43±8.26 | 45.36±12.40 | ns | ||||
Xam + Betax | 38.16±4.07 | 21.51±6.15 | p<0.05 |
ns: nonsignificant, Xam: xamoterol, Betax: betaxolol
Brain region which is involved in each task is not limited to the reported one.