Evidence map›Paper›PMID 27173878›Full record

ArticleBiochemical and biophysical research communications2016

Activation of GPR30 improves exercise capacity and skeletal muscle strength in senescent female Fischer344 × Brown Norway rats.

Hao Wang, Allan Alencar, Marina Lin, Xuming Sun, Roberto T Sudo, Gisele Zapata-Sudo, Dawn A Lowe, Leanne Groban

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Skeletal muscle wasting: the estrogen side of sexual dimorphism.American journal of physiology. Cell physiology · 2022
    Review
  8. Article
  9. Mechanisms of sex differences in exercise capacity.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    Article
  10. Review
  11. Cardioprotection Induced by Activation of GPER in Ovariectomized Rats With Pulmonary Hypertension.The journals of gerontology. Series A, Biological sciences and medical sciences · 2018
    Article
  12. Article
  13. Activation of GPER ameliorates experimental pulmonary hypertension in male rats.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2017
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Hao WangDepartment of Anesthesiology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA; Internal Medicine/Molecular Medicine, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA. Electronic address: haowang@wakehealth.edu.
Allan AlencarDepartment of Anesthesiology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA; Institute of Biomedical Sciences, Drug Development Program, Federal University of Rio de Janeiro, Brazil. Electronic address: allankdc@gmail.com.
Marina LinDepartment of Anesthesiology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA. Electronic address: mlin@wakehealth.edu.
Xuming SunDepartment of Anesthesiology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA. Electronic address: xsun@wakehealth.edu.
Roberto T SudoDepartment of Anesthesiology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA; Institute of Biomedical Sciences, Drug Development Program, Federal University of Rio de Janeiro, Brazil. Electronic address: rtsudo@icb.ufrj.br.
Gisele Zapata-SudoDepartment of Anesthesiology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA; Institute of Biomedical Sciences, Drug Development Program, Federal University of Rio de Janeiro, Brazil. Electronic address: gzsudo@oi.com.br.
Dawn A LowePrograms in Rehabilitation Science and Physical Therapy, Dept. of Physical Medicine and Rehabilitation, University of Minnesota, Minneapolis, MN, USA. Electronic address: lowex017@umn.edu.
Leanne GrobanDepartment of Anesthesiology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA; Internal Medicine/Molecular Medicine, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA; The Hypertension and Vascular Research Center, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA; Sticht Center on Aging, Wake Forest School of Medicine, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, USA. Electronic address: lgroban@wakehealth.edu.
Wake Forest University · USUniversity of Minnesota · US

Funding

Interatction of Estrogen, Age and Activity on Musculoskeletal Strength in FemalesR01AG031743 · NIA · UNIVERSITY OF MINNESOTA · PI DAWN A LOWE · 2009 to 2026
$7.4M
Interplay Between Estrogen, GPR30 and Chymase/RAS in Diastolic FunctionR01AG033727 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI GROBAN, LEANNE · 2009 to 2017
$2.8M
NIA NIH HHS R01 AG031743NIA NIH HHS R01 AG033727
6 · The paper itself

Abstract

The molecular mechanisms of muscle weakness and sarcopenia in postmenopausal women are largely unknown. To determine the effect of a new estrogen receptor, GPR30, in the maintenance of exercise capacity and skeletal muscle function in females, the selective GPR30 agonist, G1 (100 μg/kg/day), or vehicle (V, soybean oil) was administered subcutaneously daily (n = 7 per group) to ovariectomized (OVX) 27-month-old Fischer 344 × Brown Norway (F344BN) female rats. Following 8 weeks of treatment, the exercise capacity (treadmill walk time to exhaustion) was reduced in OVX vs. sham rats (5.1 ± 1.4 vs. 11.0 ± 0.9 min, P < 0.05), and chronic G1 restored exercise capacity (12.9 ± 1.2 min; P < 0.05 vs. OVX-V). Similarly, the peak twitch of electrically stimulated soleus muscles was decreased by 22% in OVX vs. sham rats (P < 0.05), and G1 attenuated this decline (P < 0.05). Western blot analysis showed that chronic G1 treatment attenuated OVX-associated decreases in heat shock protein (HSP) 90, HSP70, and HSP27 expressions. In vitro studies using the L6 myoblast cell line demonstrated that G1 increased mRNA levels of HSPs in cultured cells. Collectively, these data demonstrate that the activation of GPR30 mitigates the adverse effects of estrogen loss on exercise capacity and skeletal muscle contractile function in old F344BN rats. The protective effects of GPR30 might be through its upregulation of heat shock proteins in skeletal muscle.

Indexed as

Muscle StrengthPhysical Conditioning, AnimalAnimalsApoptosisCell LineEstrogensExercise TestFemaleGene Expression RegulationHeat-Shock ProteinsMuscle ContractionMuscle, SkeletalOvariectomyRats, Inbred BNRats, Inbred F344Receptors, G-Protein-CoupledEstrogensGper1 protein, ratHeat-Shock ProteinsReceptors, G-Protein-CoupledRNA, MessengerExercise capacityFischer344 × Brown Norway ratGPR30OvariectomySkeletal muscle

Identifiers

PMID27173878
PMCPMC4884542
OpenAlexW2345318086

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.