TY - JOUR
T1 - Sighted C3H mice - A tool for analysing the influence of vision on mouse behaviour?
AU - Hoelter, Sabine M.
AU - Dalke, Claudia
AU - Kallnik, Magdalena
AU - Becker, Lore
AU - Horsch, Marion
AU - Schrewe, Anja
AU - Favor, Jack
AU - Klopstock, Thomas
AU - Beckers, Johannes
AU - Ivandic, Boris
AU - Gailus-Durner, Valérie
AU - Fuchs, Helmut
AU - De Angelis, Martin Hrabé
AU - Graw, Jochen
AU - Wurst, Wolfgang
PY - 2008/5/1
Y1 - 2008/5/1
N2 - It is unclear what role vision plays in guiding mouse behaviour, since the mouse eye is of comparably low optical quality, and mice are considered to rely primarily on other senses. All C3H substrains are homozygous for the Pde6b rd1 mutation and get blind by weaning age. To study the impact of the Pde6brd1 mutation on mouse behaviour and physiology, sighted C3H (C3H.Pde6b+) and normal C3H/HeH mice were phenotyped for different aspects. We confirmed retinal degeneration 1 in C3H/HeH mice, and the presence of a morphologically normal retina as well as visual ability in C3H.Pde6b+ mice. However, C3H.Pde6b+ mice showed an abnormal retinal function in the electroretinogram response, indicating that their vision was not normal as expected. C3H.Pde6b+ mice showed reduced latencies for several behaviours without any further alterations in these behaviours in comparison to C3H/HeH mice, suggesting that visual ability, although impaired, enables earlier usage of the behavioural repertoire in a novel environment, but does not lead to increased activity levels. These results emphasize the importance of comprehensive behavioural and physiological phenotyping.
AB - It is unclear what role vision plays in guiding mouse behaviour, since the mouse eye is of comparably low optical quality, and mice are considered to rely primarily on other senses. All C3H substrains are homozygous for the Pde6b rd1 mutation and get blind by weaning age. To study the impact of the Pde6brd1 mutation on mouse behaviour and physiology, sighted C3H (C3H.Pde6b+) and normal C3H/HeH mice were phenotyped for different aspects. We confirmed retinal degeneration 1 in C3H/HeH mice, and the presence of a morphologically normal retina as well as visual ability in C3H.Pde6b+ mice. However, C3H.Pde6b+ mice showed an abnormal retinal function in the electroretinogram response, indicating that their vision was not normal as expected. C3H.Pde6b+ mice showed reduced latencies for several behaviours without any further alterations in these behaviours in comparison to C3H/HeH mice, suggesting that visual ability, although impaired, enables earlier usage of the behavioural repertoire in a novel environment, but does not lead to increased activity levels. These results emphasize the importance of comprehensive behavioural and physiological phenotyping.
KW - Behaviour
KW - C3H mice
KW - Pde6b
KW - Phenotyping
KW - Vision
UR - http://www.scopus.com/inward/record.url?scp=52049125697&partnerID=8YFLogxK
U2 - 10.2741/3118
DO - 10.2741/3118
M3 - Article
C2 - 18508624
AN - SCOPUS:52049125697
SN - 2768-6701
VL - 13
SP - 5810
EP - 5823
JO - Frontiers in Bioscience
JF - Frontiers in Bioscience
IS - 15
ER -