scholarly journals Anxiety and Cognition in Cre- Collagen Type II Sirt1 K/O Male Mice

2021 ◽  
Vol 12 ◽  
Author(s):  
Biana Shtaif ◽  
Shay Henry Hornfeld ◽  
Michal Yackobovitch-Gavan ◽  
Moshe Phillip ◽  
Galia Gat-Yablonski

IntroductionUsing transgenic collagen type II-specific Sirt1 knockout (CKO) mice we studied the role of Sirt1 in nutritional induced catch up growth (CUG) and we found that these mice have a less organized growth plate and reduced efficiency of CUG. In addition, we noted that they weigh more than control (CTL) mice. Studying the reason for the increased weigh, we found differences in activity and brain function.MethodsSeveral tests for behavior and activity were used: open field; elevated plus maze, Morris water maze, and home cage running wheels. The level of Glu- osteocalcin, known to connect bone and brain function, was measured by Elisa; brain Sirt1 was analyzed by western blot.ResultsWe found that CKO mice had increased anxiety, with less spatial memory, learning capabilities and reduced activity in their home cages. No significant differences were found between CKO and CTL mice in Glu- osteocalcin levels; nor in the level of brain SIRT1.Discussion/ConclusionUsing transgenic collagen type II-specific Sirt1 knockout (CKO) mice we found a close connection between linear growth and brain function. Using a collagen type II derived system we affected a central regulatory mechanism leading to hypo activity, increased anxiety, and slower learning, without affecting circadian period. As children with idiopathic short stature are more likely to have lower IQ, with substantial deficits in working memory than healthy controls, the results of the current study suggest that SIRT1 may be the underlying factor connecting growth and brain function.

2020 ◽  
Vol 6 (4) ◽  
pp. 747-750
Author(s):  
Dr. Sathik Babu ◽  
Dr. Pradeep Elangovan ◽  
Dr. Dinesh Kumar S

2003 ◽  
Vol 995 (1) ◽  
pp. 140-150 ◽  
Author(s):  
ERIKA GUSTAFSSON ◽  
ATTILA ASZÓDI ◽  
NATHALIE ORTEGA ◽  
ERNST B. HUNZIKER ◽  
HANS-WERNER DENKER ◽  
...  

2008 ◽  
Vol 36 (6) ◽  
pp. 1597-1604 ◽  
Author(s):  
Qiaomei Dai ◽  
Jianghong Fang ◽  
Feng-shan Zhang

2000 ◽  
Vol 13 (04) ◽  
pp. 178-184 ◽  
Author(s):  
D. T. Crouch ◽  
D. D. Lewis ◽  
J. M. Kreeger ◽  
J. L. Tomlinson ◽  
J. L. Cook

SummaryThe purpose of this study was to determine collagen type II and X immunohistochemical staining characteristics of naturally-occurring fragmented medial coronoid processes (FMCP) in order to help delineate potential pathophysiological events associated with FMCP.34 surgically excised FMCP from 21 client-owned dogs and 16 intact medial coronoid processes from 8 mongrel dogs were examined. The specimens were categorized by the dog's age: <12 months, 12–18 months, 18–24 months, >24 months.The excised FMCP and normal medial coronoid processes were sectioned and stained with haematoxylin and eosin, safranin-O fast green, and toluidine blue. Sections were subjectively evaluated for tissue morphology, cell and matrix content, and proteoglycan staining. Immunohistochemical staining was performed for collagen types II and X. Sections were then subjectively evaluated for the location and intensity of staining.FMCP tissue demonstrated a wide variety of histological and immunohistochemical characteristics compared to normal medial coronoid processes. Significantly (P = 0.016) more normal dogs stained positive for collagen type X than dogs with FMCP in the <12 months old group. No other significant differences between affected and normal dogs were noted for either collagen type in any age group. No significant difference in age was noted for the presence or absence of collagen type II among affected dogs, and no statistically significant correlation was observed between age of those with collagens type X and type II present. Although not statistically significant (P = 0.100), there was a trend for the presence of collagen type II when collagen type X was present. The results of this study have not provided a definitive answer regarding the role of collagen type X in the etiopathogenesis of FMCP, but suggest that it may be an important factor in some cases, warranting further investigation. Excised fragmented medial coronoid processes were examined to determine the collagen immunohistochemical staining characteristics when compared to intact processes.


1992 ◽  
Vol 22 (1) ◽  
pp. 51-56 ◽  
Author(s):  
Tan Yan ◽  
Harald Burkhardt ◽  
Thomas Ritter ◽  
Barbara Bröker ◽  
Karl Heinz Mann ◽  
...  

1995 ◽  
Vol 40 (3) ◽  
pp. 181-185 ◽  
Author(s):  
H. Devlin ◽  
J. Hoyland ◽  
A.J. Freemont ◽  
P. Sloan

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