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Record W7030147934

Microvascular Function and Remodeling Due to Chronic Changes Within the Skeletal Muscle Microenvironment

2016· other· en· W7030147934 on OpenAlexafffund

Bibliographic record

VenueYorkSpace (York University) · 2016
Typeother
Languageen
FieldComputer Science
TopicHistory of Computing Technologies
Canadian institutionsYork University
FundersYork University
KeywordsArteriogenesisMicrocirculationAngiogenesisTIMP1Vascular remodelling in the embryoBlood vesselVascular smooth muscleVasodilationMatrix metalloproteinaseBlood flow
DOInot available

Abstract

fetched live from OpenAlex

The skeletal muscle microcirculation is a key regulator of local blood distribution, vascular resistance and overall blood pressure (BP). Arterioles and capillaries are two important components of the microcirculation, which can undergo remodeling such as arteriogenesis, angiogenesis, or capillary rarefaction. Vascular remodeling requires the coordinated action of several factors within the microenvironment. These include: matrix metalloproteinases (MMPs) and their endogenous inhibitors, tissue inhibitor of metalloproteinases (TIMPs), vascular endothelial growth factor-A (VEGF-A) and thrombospondin-1 (TSP-1). The objective of this dissertation was to examine how alterations to the microenvironment impacted the appropriate microvascular remodeling responses to alterations in flow. The skeletal muscle microenvironment was altered through manipulation of TIMP1 expression or glucocorticoid (GC) levels. Furthermore, blood flow was altered via femoral artery (FA) ligation or prazosin treatment. This dissertation includes three primary hypotheses and corresponding findings to examine the importance of alterations to the microenvironment on microvascular remodeling. Firstly, the loss of TIMP1 would enhance both ischemia and flow-induced vascular remodeling by increasing MMP activity. Using TIMP1 deficient mice (Timp1-/-), we demonstrated that TIMP1 is integral for vascular network maturation. Additionally, TIMP1 is required for microvascular adaptations to alterations in flow. This was proven by the absence of arteriogenesis and/or angiogenesis in Timp1-/- mice in response to elevations in flow despite an increase in both VEGF-A and eNOS mRNA. Secondly, Corticosterone (CORT) treatment would inhibit endothelial mediated shear stress signaling and subsequently, the microvascular remodeling responses to prazosin administration. Lastly, CORT mediated hypertension and microcirculatory rarefaction would be prevented with 2 weeks of concurrent prazosin or Tempol (a ROS scavenger) administration. Endothelial cell responsiveness to shear stress was partially blunted by CORT pre-treatment. The lack of vascular remodeling (angiogenesis and arteriogenesis) and prevention of GC-mediated capillary rarefaction in CORT-prazosin animals supports this finding. The maintenance of vascular tone and skeletal muscle blood flow, more so then lowering circulating levels of ROS, was responsible for mitigating CORT-induced capillary rarefaction and hypertension. Taken together, these three studies demonstrate that perturbations of the microenvironment, due to the loss of TIMP1 or elevated GCs, results in impaired microvascular remodeling to alterations in flow. Furthermore, alterations to the skeletal muscle microcirculation can impact overall cardiovascular health.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Methods · Consensus signal: none
Teacher disagreement score0.872
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0020.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.008
GPT teacher head0.166
Teacher spread0.159 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designNot applicable
Domainnot available
GenreMethods

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2016
Admission routes2
Has abstractyes

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