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Intestinal stearoyl-CoA desaturase-1 (SCD1) is differentially expressed along the intestinal length and is regulated through dietary manipulation

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Title
Intestinal stearoyl-CoA desaturase-1 (SCD1) is differentially expressed along the intestinal length and is regulated through dietary manipulation
Name (type = personal)
NamePart (type = family)
Akal
NamePart (type = given)
Tasleenpal Kaur
DisplayForm
Tasleenpal Kaur Akal
Role
RoleTerm (authority = RULIB)
author
Name (type = personal)
NamePart (type = family)
Sampath
NamePart (type = given)
Harini
DisplayForm
Harini Sampath
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
chair
Name (type = personal)
NamePart (type = family)
Miller
NamePart (type = given)
Joshua
DisplayForm
Joshua Miller
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
internal member
Name (type = personal)
NamePart (type = family)
Bello
NamePart (type = given)
Nicholas
DisplayForm
Nicholas Bello
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
internal member
Name (type = corporate)
NamePart
Rutgers University
Role
RoleTerm (authority = RULIB)
degree grantor
Name (type = corporate)
NamePart
School of Graduate Studies
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RoleTerm (authority = RULIB)
school
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Text
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theses
OriginInfo
DateCreated (encoding = w3cdtf); (keyDate = yes); (qualifier = exact)
2020
DateOther (encoding = w3cdtf); (qualifier = exact); (type = degree)
2020-05
Language
LanguageTerm (authority = ISO 639-3:2007); (type = text)
English
Abstract (type = abstract)
Stearoyl-CoA desaturase (SCD) is an enzyme that catalyzes the formation of monounsaturated fatty acids from saturated fatty acids. Primarily, the enzyme converts palmitoyl-CoA and stearoyl-CoA to palmitoleoyl-CoA and oleoyl-CoA, respectively. Previous studies have shown that this enzyme is transcriptionally regulated in numerous metabolically-important tissues, such as liver and adipose, in response to nutritional manipulation. However, virtually nothing is known regarding its potential expression and regulation in the intestine, the primary site of lipid absorption in the body. In this study, we aimed to identify whether SCD1 is expressed in the intestine and whether it is regulated in a manner similar to a lipogenic tissue such as liver. Age-matched male wild type C57BL/6J were fasted for 24 hours and then refed a lipogenic high-sucrose very low fat diet (HSVLF) for 16 hours, a paradigm that is known to transcriptionally activate Scd1 in the liver. Mucosal scrapings were collected from duodenum, proximal jejunum, distal jejunum, ileum and colon. Results show that this refeeding protocol increases SCD1 mRNA and protein expression in duodenum, proximal jejunum, distal jejunum, and ileum. This was also true for several other lipogenic genes, such as sterol regulatory element binding protein (Srebp-1c), acetyl-CoA carboxylase (Acc), and fatty acid synthase (Fas). SCD1 was expressed at the highest level in the ileum in comparison to duodenum and both proximal and distal sections of jejunum. Immunohistological analyses of Swiss-rolled sections of small intestine showed an increase in SCD1 protein expression after refeeding as well differential SCD1 expression along the length of the intestine, corroborating gene expression data. We conclude that SCD1 is differentially expressed throughout the intestine and is regulated through dietary manipulation.
Subject (authority = RUETD)
Topic
Nutritional Sciences
Subject (authority = LCSH)
Topic
Digestive enzymes
RelatedItem (type = host)
TitleInfo
Title
Rutgers University Electronic Theses and Dissertations
Identifier (type = RULIB)
ETD
Identifier
ETD_10794
PhysicalDescription
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application/pdf
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text/xml
Extent
1 online resource (vii, 37 pages) : illustrations
Note (type = degree)
M.S.
Note (type = bibliography)
Includes bibliographical references
RelatedItem (type = host)
TitleInfo
Title
School of Graduate Studies Electronic Theses and Dissertations
Identifier (type = local)
rucore10001600001
Location
PhysicalLocation (authority = marcorg); (displayLabel = Rutgers, The State University of New Jersey)
NjNbRU
Identifier (type = doi)
doi:10.7282/t3-t727-0x82
Genre (authority = ExL-Esploro)
ETD graduate
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RightsDeclaration (ID = rulibRdec0006)
The author owns the copyright to this work.
RightsHolder (type = personal)
Name
FamilyName
Akal
GivenName
Tasleenpal Kaur
Role
Copyright Holder
RightsEvent
Type
Permission or license
DateTime (encoding = w3cdtf); (qualifier = exact); (point = start)
2020-04-21 15:32:30
AssociatedEntity
Name
Tasleenpal Akal
Role
Copyright holder
Affiliation
Rutgers University. School of Graduate Studies
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Type
License
Name
Author Agreement License
Detail
I hereby grant to the Rutgers University Libraries and to my school the non-exclusive right to archive, reproduce and distribute my thesis or dissertation, in whole or in part, and/or my abstract, in whole or in part, in and from an electronic format, subject to the release date subsequently stipulated in this submittal form and approved by my school. I represent and stipulate that the thesis or dissertation and its abstract are my original work, that they do not infringe or violate any rights of others, and that I make these grants as the sole owner of the rights to my thesis or dissertation and its abstract. I represent that I have obtained written permissions, when necessary, from the owner(s) of each third party copyrighted matter to be included in my thesis or dissertation and will supply copies of such upon request by my school. I acknowledge that RU ETD and my school will not distribute my thesis or dissertation or its abstract if, in their reasonable judgment, they believe all such rights have not been secured. I acknowledge that I retain ownership rights to the copyright of my work. I also retain the right to use all or part of this thesis or dissertation in future works, such as articles or books.
RightsEvent
Type
Embargo
DateTime (encoding = w3cdtf); (qualifier = exact); (point = start)
2020-05-31
DateTime (encoding = w3cdtf); (qualifier = exact); (point = end)
2022-05-31
Detail
Access to this PDF has been restricted at the author's request. It will be publicly available after May 31st, 2022.
Copyright
Status
Copyright protected
Availability
Status
Open
Reason
Permission or license
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Technical

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ETD
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windows xp
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1.7
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Microsoft® Word for Office 365
DateCreated (point = end); (encoding = w3cdtf); (qualifier = exact)
2020-04-20T17:22:45
DateCreated (point = end); (encoding = w3cdtf); (qualifier = exact)
2020-04-20T17:22:45
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