Cited by 119Metabolism, Diabetes, and CancerMuscle metabolism and nutritionCardiovascular and exercise physiology

The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.

Increased AS160 phosphorylation, but not TBC1D1 phosphorylation, with increased postexercise insulin sensitivity in rat skeletal muscle

Open access
Funai, Katsuhiko, Schweitzer, George G., Sharma, Naveen, Kanzaki, Makoto, Cartee, Gregory D.·2009·American Journal of Physiology-Endocrinology and Metabolism

Abstract

A single exercise bout can increase insulin-independent glucose transport immediately postexercise and insulin-dependent glucose transport (GT) for several hours postexercise. Akt substrate of 160 kDa (AS160) and TBC1D1 are paralog Rab GTPase-activating proteins that have been proposed to contribute to these exercise effects. Previous research demonstrated greater AS160 and Akt threonine phosphorylation in rat skeletal muscle at 3–4 h postexercise concomitant with enhanced insulin-stimulated GT. To further probe whether these signaling events or TBC1D1 phosphorylation were important for the enhanced postexercise insulin-stimulated GT, male Wistar rats were studied using four experimental protocols (2-h swim exercise, differing with regard to timing of muscle sampling and whether food was provided postexercise) that were known to vary in their influence of insulin-independent and insulin-dependent GT postexercise. The results indicated that, in isolated rat epitrochlearis muscle, 1) elevated phosphorylation of AS160 (measured using anti-phospho-Akt substrate, PAS-AS160, and phosphospecific anti-Thr 642-AS160, pThr 642-AS160) consistently tracked with elevated insulin-stimulated GT; 2) PAS-TBC1D1 was not different from sedentary values at 3 or 27 h postexercise, when insulin sensitivity was increased; 3) insulin-stimulated Akt activity was not increased postexercise in muscles with increased insulin sensitivity; 4) PAS-TBC1D1 was increased immediately postexercise, when insulin-independent GT was elevated, and reversed at 3 and 27 h postexercise, when insulin-independent GT was also reversed; and 5) there was no significant effect of exercise or insulin on total abundance of AS160, TBC1D1, Akt, or GLUT4 protein with any of the protocols. The results are consistent with increased AS160 phosphorylation (PAS-AS160 or pThr 642-AS160) but not increased PAS-TBC1D1 or Akt activity, which is important for increased postexercise insulin-stimulated GT in rat skeletal muscle. They also support the idea that increased TBC1D1 phosphorylation may play a role in the insulin-independent increase in GT postexercise.

Overview

Integrity signals

Registry

Crossref · 10.1152/ajpendo.00194.2009

Cites

56 of 56 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Refeeding rather than fasting following exercise reduced the enhanced effects of insulin on glucose uptake as well as TBC1D4 T642 and PAS phosphorylation.

    “Funai et al. [142] found that refeeding rather than fasting following exercise reduced the enhanced effects of insulin on glucose uptake as well as TBC1D4 T642 and PAS phosphorylation.”

    From AMPK and Exercise: Glucose Uptake and Insulin Sensitivity (2013) · cites this paper as [142]

Citations

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Metadata

Authors
Funai, K., Schweitzer, G. G., Sharma, N., Kanzaki, M., & Cartee, G. D.
Affiliations
University of Michigan (US)
Venue
American Journal of Physiology-Endocrinology and Metabolism
Published
2009-07
Volume
297
Issue
1
Pages
E242-E251
ISSN
  • 0193-1849 (ISSN-L)
  • 1522-1555
OpenAlex
W1985381832
Cited by
119
References
56
Citations by year
2026: 3 · 2025: 2 · 2024: 6 · 2023: 4 · 2022: 2 · 2021: 8 · 2020: 5 · 2019: 10 · 2018: 10 · 2017: 11 · 2016: 9 · 2015: 11 · 2014: 13 · 2013: 4 · 2012: 7
FWCI
2.82
Type
journal article
Language
en
Open access
Locations
  • American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01ag011026-21)
  • National Institute on Aging (AG-011026)
  • National Institute of Diabetes and Digestive and Kidney Diseases (DK071771, R01DK071771)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
  • Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
  • Health Sciences › Medicine › Physiology (medical) › Cardiovascular and exercise physiology
Keywords
AS160 phosphorylation, insulin sensitivity, insulin-independent glucose transport, insulin-stimulated glucose transport, Akt signaling, Rab GTPase-activating protein, skeletal muscle, epitrochlearis muscle, GLUT4, physical activity
MeSH terms
Animals, Biological Transport, Glucose, Glycogen, Insulin Resistance, Male, Phosphorylation, Physical Conditioning, Animal, Protein Kinases, Proteins, Threonine, Up-Regulation, Rats, Wistar, Muscle, Skeletal, GTPase-Activating Proteins, Oncogene Protein v-akt, Rats

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review