Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Manganese toxicity: Accumulation in ...
~
O'Neal, Stefanie L.
Linked to FindBook
Google Book
Amazon
博客來
Manganese toxicity: Accumulation in bone, effect on brain neurochemistry, and impact on adult neurogenesis.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Manganese toxicity: Accumulation in bone, effect on brain neurochemistry, and impact on adult neurogenesis./
Author:
O'Neal, Stefanie L.
Published:
Ann Arbor : ProQuest Dissertations & Theses, : 2015,
Description:
206 p.
Notes:
Source: Dissertation Abstracts International, Volume: 77-09(E), Section: B.
Contained By:
Dissertation Abstracts International77-09B(E).
Subject:
Toxicology. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10106198
ISBN:
9781339696485
Manganese toxicity: Accumulation in bone, effect on brain neurochemistry, and impact on adult neurogenesis.
O'Neal, Stefanie L.
Manganese toxicity: Accumulation in bone, effect on brain neurochemistry, and impact on adult neurogenesis.
- Ann Arbor : ProQuest Dissertations & Theses, 2015 - 206 p.
Source: Dissertation Abstracts International, Volume: 77-09(E), Section: B.
Thesis (Ph.D.)--Purdue University, 2015.
Manganese (Mn) exposure is a growing public health concern as new evidence continues to show that high level exposure to this essential metal is toxic. Chiefly toxic to the central nervous system, it produces signs and symptoms resembling, but not identical to idiopathic Parkinson's disease. The hypothesis tested in this dissertation is that Mn accumulation in body tissues produces subclinical changes in the central nervous system altering neuronal repair mechanisms and leading to neurodegenerative damage. The studies in this dissertation evaluated the extent of these changes in the central nervous system. Changes in the toxicokinetic properties of Mn in bone affecting the parameters of accumulation, distribution, and elimination were also identified. Importantly, the half-life of Mn in bone was estimated to be approximately 8.6 years in humans, a finding which will be essential in developing a biomonitoring system for Mn exposure. Significant accumulation of Mn in brain and body tissues was observed along with significant metal dyshomeostasis following Mn exposure. Several brain regions had altered neurochemistry, and as a consequence, impaired motor function was observed. The subventricular zone (SVZ), one of two neurogenic niches in the adult brain, had the largest magnitude of change. Therefore, effects of Mn exposure on cell proliferation and differentiation in this region were investigated further. The processes involved in adult neurogenesis were significantly altered following Mn exposure, particularly with regard to cell proliferation. The full extent of the consequences resulting from Mn exposure in the pathology of neurodegenerative disease remains unknown, but the results of these studies demonstrate that although Mn exposure undoubtedly leads to several changes observed early in neurodegenerative disease pathology, no overt neurodegeneration was observed. The results of this work will help researchers studying the effect of metal exposure on adult neurogenesis and will also help researchers studying neurodegenerative disease and other disorders of the central nervous system.
ISBN: 9781339696485Subjects--Topical Terms:
556884
Toxicology.
Manganese toxicity: Accumulation in bone, effect on brain neurochemistry, and impact on adult neurogenesis.
LDR
:03097nmm a2200313 4500
001
2122387
005
20170922124909.5
008
180830s2015 ||||||||||||||||| ||eng d
020
$a
9781339696485
035
$a
(MiAaPQ)AAI10106198
035
$a
AAI10106198
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
O'Neal, Stefanie L.
$3
3284355
245
1 0
$a
Manganese toxicity: Accumulation in bone, effect on brain neurochemistry, and impact on adult neurogenesis.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2015
300
$a
206 p.
500
$a
Source: Dissertation Abstracts International, Volume: 77-09(E), Section: B.
500
$a
Adviser: Wei Zheng.
502
$a
Thesis (Ph.D.)--Purdue University, 2015.
520
$a
Manganese (Mn) exposure is a growing public health concern as new evidence continues to show that high level exposure to this essential metal is toxic. Chiefly toxic to the central nervous system, it produces signs and symptoms resembling, but not identical to idiopathic Parkinson's disease. The hypothesis tested in this dissertation is that Mn accumulation in body tissues produces subclinical changes in the central nervous system altering neuronal repair mechanisms and leading to neurodegenerative damage. The studies in this dissertation evaluated the extent of these changes in the central nervous system. Changes in the toxicokinetic properties of Mn in bone affecting the parameters of accumulation, distribution, and elimination were also identified. Importantly, the half-life of Mn in bone was estimated to be approximately 8.6 years in humans, a finding which will be essential in developing a biomonitoring system for Mn exposure. Significant accumulation of Mn in brain and body tissues was observed along with significant metal dyshomeostasis following Mn exposure. Several brain regions had altered neurochemistry, and as a consequence, impaired motor function was observed. The subventricular zone (SVZ), one of two neurogenic niches in the adult brain, had the largest magnitude of change. Therefore, effects of Mn exposure on cell proliferation and differentiation in this region were investigated further. The processes involved in adult neurogenesis were significantly altered following Mn exposure, particularly with regard to cell proliferation. The full extent of the consequences resulting from Mn exposure in the pathology of neurodegenerative disease remains unknown, but the results of these studies demonstrate that although Mn exposure undoubtedly leads to several changes observed early in neurodegenerative disease pathology, no overt neurodegeneration was observed. The results of this work will help researchers studying the effect of metal exposure on adult neurogenesis and will also help researchers studying neurodegenerative disease and other disorders of the central nervous system.
590
$a
School code: 0183.
650
4
$a
Toxicology.
$3
556884
650
4
$a
Neurosciences.
$3
588700
650
4
$a
Environmental health.
$3
543032
650
4
$a
Biochemistry.
$3
518028
690
$a
0383
690
$a
0317
690
$a
0470
690
$a
0487
710
2
$a
Purdue University.
$b
Health Sciences.
$3
3284356
773
0
$t
Dissertation Abstracts International
$g
77-09B(E).
790
$a
0183
791
$a
Ph.D.
792
$a
2015
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10106198
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9333003
電子資源
01.外借(書)_YB
電子書
EB
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login