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Record W4403397626 · doi:10.1161/hyp.81.suppl_1.p448

Abstract P448: Follistatin Improves Vascular Function by Regulating Perivascular Adipose Tissue in Essential Hypertension

2024· article· en· W4403397626 on OpenAlexaff
Ann Kuganathan, Vincent Lu, Bo Gao, Melissa E. MacDonald, Jeffrey G. Dickhout, Joan C. Krepinsky

Bibliographic record

VenueHypertension · 2024
Typearticle
Languageen
FieldMedicine
TopicCardiovascular Disease and Adiposity
Canadian institutionsMcMaster University
Fundersnot available
KeywordsFollistatinAdipose tissueMedicineInternal medicineEndocrinologyFunction (biology)PathologyBiologyCell biology

Abstract

fetched live from OpenAlex

Introduction: Essential hypertension is characterized by resistance artery remodeling induced by oxidative stress. Most vessels are surrounded by perivascular adipose tissue (PVAT) which regulates vascular tone via release of vasoactive substances. In physiological conditions, PVAT induces an anticontractile effect. In pathological conditions such as hypertension, PVAT exhibit increased oxidative stress resulting in augmented contraction and reduced relaxation. Follistatin, an antioxidant glycoprotein, has been shown to induce adipose tissue browning which is linked to improved vasorelaxation and BP. We hypothesize that follistatin, through ROS inhibition and PVAT browning, lowers BP and improves vessel function in a model of essential hypertension. Methods: Spontaneously hypertensive rats (SHR) were treated with vehicle or follistatin every other day for 8 weeks. Wistar Kyoto (WKY) rats served as normotensive controls. BP was measured weekly by radiotelemetry. Mesenteric arteries and PVAT were used. KCl-induced smooth muscle contraction was assessed using wire myography. ROS was measured by DHE (dihydroethidium) staining. Vasodilator nitric oxide (NO) bioavailability in PVAT was measured using DAF-2 FM. Protein expression of markers for ROS or PVAT browning was measured by immunohistochemistry. Results: Follistatin significantly lowered BP in SHRs and restored anticontractile effect of PVAT. Increased ROS in SHR vessels and PVAT were also inhibited. Follistatin inhibited SHR PVAT-induced vascular oxidative stress. SHR PVAT NO bioavailability was increased by acute follistatin treatment via ROS inhibition. Follistatin also increased expression of brown adipose tissue markers in SHR PVAT suggesting PVAT browning. Limitations: Above studies do not confirm whether PVAT pathology causes hypertension in this model. Vascular dysfunction is an independent risk factor for CVD and our studies do not yet consider effects of follistatin on end-organ damage. Conclusions: Follistatin lowers BP in SHRs likely via improved vascular and perivascular structure and function. Specifically, follistatin inhibited perivascular ROS, increased NO and induced PVAT browning suggesting improved regulation of vascular function and thus, BP. Future work will utilize proteomic assays to identify novel mediators of follistatin effects on PVAT in the SHR.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.007
Threshold uncertainty score0.022

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0070.001

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 head0.010
GPT teacher head0.231
Teacher spread0.221 · 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 source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

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
Published2024
Admission routes1
Has abstractyes

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