Evidence map›Paper›PMID 26474831›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Beneficial effects of growth hormone-releasing hormone agonists on rat INS-1 cells and on streptozotocin-induced NOD/SCID mice.

Xianyang Zhang, Tengjiao Cui, Jinlin He, Haibo Wang, Renzhi Cai, Petra Popovics, Irving Vidaurre, Wei Sha, Janine Schmid, Barbara Ludwig and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. GHRH in diabetes and metabolism.Reviews in endocrine & metabolic disorders · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. GHRH agonist MR-409 protects β-cells from streptozotocin-induced diabetes.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. Agonist of growth hormone-releasing hormone improves the disease features of spinal muscular atrophy mice.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Agonistic analog of growth hormone-releasing hormone promotes neurofunctional recovery and neural regeneration in ischemic stroke.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

13 authors at 3 institutions in 2 countries.

Xianyang ZhangInterdisciplinary Stem Cell Institute, Miller School of Medicine, University of Miami, Miami, FL 33136; Endocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; South Florida Veterans Affairs Foundation for Research and Education, Miami, FL 33125; xyzhang@med.miami.edu andrew.schally@va.gov.
Tengjiao CuiInterdisciplinary Stem Cell Institute, Miller School of Medicine, University of Miami, Miami, FL 33136; Endocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; South Florida Veterans Affairs Foundation for Research and Education, Miami, FL 33125;
Jinlin HeEndocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; South Florida Veterans Affairs Foundation for Research and Education, Miami, FL 33125;
Haibo WangInterdisciplinary Stem Cell Institute, Miller School of Medicine, University of Miami, Miami, FL 33136; Endocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125;
Renzhi CaiInterdisciplinary Stem Cell Institute, Miller School of Medicine, University of Miami, Miami, FL 33136; Endocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; South Florida Veterans Affairs Foundation for Research and Education, Miami, FL 33125;
Petra PopovicsEndocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; Department of Medicine III, University Hospital Carl Gustav Carus, 01307 Dresden, Germany;
Irving VidaurreEndocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; South Florida Veterans Affairs Foundation for Research and Education, Miami, FL 33125;
Wei ShaInterdisciplinary Stem Cell Institute, Miller School of Medicine, University of Miami, Miami, FL 33136; Endocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125;
Janine SchmidDepartment of Medicine III, University Hospital Carl Gustav Carus, 01307 Dresden, Germany;
Barbara LudwigDepartment of Medicine III, University Hospital Carl Gustav Carus, 01307 Dresden, Germany;
Norman L BlockEndocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; South Florida Veterans Affairs Foundation for Research and Education, Miami, FL 33125; Department of Pathology, Miller School of Medicine, University of Miami, Miami, FL 33136; Division of Hematology and Oncology, Department of Medicine, Miller School of Medicine, University of Miami, Miami, FL 33136;
Stefan R BornsteinDepartment of Medicine III, University Hospital Carl Gustav Carus, 01307 Dresden, Germany;
Andrew V SchallyEndocrine, Polypeptide, and Cancer Institute, Veterans Affairs Medical Center, Miami, FL 33125; South Florida Veterans Affairs Foundation for Research and Education, Miami, FL 33125; Department of Pathology, Miller School of Medicine, University of Miami, Miami, FL 33136; Division of Hematology and Oncology, Department of Medicine, Miller School of Medicine, University of Miami, Miami, FL 33136; Division of Endocrinology, Department of Medicine, Miller School of Medicine, University of Miami, Miami, FL 33136 xyzhang@med.miami.edu andrew.schally@va.gov.
South Florida Veterans Affairs Foundation for Research and Education · USUniversity Hospital Carl Gustav Carus · DEUniversity of Miami · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Agonists of growth hormone-releasing hormone (GHRH) have been previously reported to promote growth, function, and engraftment of islet cells following transplantation. Here we evaluated recently synthesized GHRH agonists on the proliferation and biological functions of rat pancreatic β-cell line (INS-1) and islets. In vitro treatment of INS-1 cells with GHRH agonists increased cell proliferation, the expression of cellular insulin, insulin-like growth factor-1 (IGF1), and GHRH receptor, and also stimulated insulin secretion in response to glucose challenge. Exposure of INS-1 cells to GHRH agonists, MR-356 and MR-409, induced activation of ERK and AKT pathways. Agonist MR-409 also significantly increased the levels of cellular cAMP and the phosphorylation of cAMP response element binding protein (CREB) in INS-1 cells. Treatment of rat islets with agonist, MR-409 significantly increased cell proliferation, islet size, and the expression of insulin. In vivo daily s.c. administration of 10 μg MR-409 for 3 wk dramatically reduced the severity of streptozotocin (STZ)-induced diabetes in nonobese diabetic severe combined immunodeficiency (NOD/SCID) mice. The maximal therapeutic benefits with respect to the efficiency of engraftment, ability to reach normoglycemia, gain in body weight, response to high glucose challenge, and induction of higher levels of serum insulin and IGF1 were observed when diabetic mice were transplanted with rat islets preconditioned with GHRH agonist, MR-409, and received additional treatment with MR-409 posttransplantation. This study provides an improved approach to the therapeutic use of GHRH agonists in the treatment of diabetes mellitus.

Indexed as

AnimalsCell Line, TumorGrowth Hormone-Releasing HormoneMiceMice, Inbred NODMice, SCIDRatsStreptozocinGrowth Hormone-Releasing HormoneStreptozocindiabetesGHRH agonistsINS-1signaling pathwaystransplantation

Identifiers

PMID26474831
PMCPMC4640729
OpenAlexW2206985864

What OpenQuestion holds

Textmetadata
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.