Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12

Cholinesterase (ChE) activity in the chondrocranium of normal and exencephalic trisomy 12 mouse fetuses was studied. Non-specific cholinesterase activity was found strongly in the developing bone cells at the central zone and weakly in the more maturely developed bone cells at the peripheral zone of...

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Main Authors: Theetranont C., Vanittanakom P., Gropp A.
Format: Article
Language:English
Published: 2014
Online Access:http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3551
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-35512014-08-30T02:35:01Z Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12 Theetranont C. Vanittanakom P. Gropp A. Cholinesterase (ChE) activity in the chondrocranium of normal and exencephalic trisomy 12 mouse fetuses was studied. Non-specific cholinesterase activity was found strongly in the developing bone cells at the central zone and weakly in the more maturely developed bone cells at the peripheral zone of the chondrocranium of both normal and exencephalic trisomy 12 mouse fetuses. In exencephalic mouse fetuses, the ChE-activity was lesser than in the normal ones which corresponded to hypoplastic chondrocranium. The centrifugal direction of the maturity of individual bone cells could be demonstrated by the activity of cholinesterase. The young bone cells showed strong ChE-activity while the more matured cells showed weak ChE-activity. The enzyme activity disappeared when the definite tissue structure was well developed. From this study, it may be concluded that ChE plays a role in chondrocranium development which is different from its known function in the adult tissue. 2014-08-30T02:35:01Z 2014-08-30T02:35:01Z 1992 Journal Article 0125-2208 1506793 http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/3551 eng
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
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language English
description Cholinesterase (ChE) activity in the chondrocranium of normal and exencephalic trisomy 12 mouse fetuses was studied. Non-specific cholinesterase activity was found strongly in the developing bone cells at the central zone and weakly in the more maturely developed bone cells at the peripheral zone of the chondrocranium of both normal and exencephalic trisomy 12 mouse fetuses. In exencephalic mouse fetuses, the ChE-activity was lesser than in the normal ones which corresponded to hypoplastic chondrocranium. The centrifugal direction of the maturity of individual bone cells could be demonstrated by the activity of cholinesterase. The young bone cells showed strong ChE-activity while the more matured cells showed weak ChE-activity. The enzyme activity disappeared when the definite tissue structure was well developed. From this study, it may be concluded that ChE plays a role in chondrocranium development which is different from its known function in the adult tissue.
format Article
author Theetranont C.
Vanittanakom P.
Gropp A.
spellingShingle Theetranont C.
Vanittanakom P.
Gropp A.
Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12
author_facet Theetranont C.
Vanittanakom P.
Gropp A.
author_sort Theetranont C.
title Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12
title_short Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12
title_full Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12
title_fullStr Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12
title_full_unstemmed Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12
title_sort cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12
publishDate 2014
url http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3551
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