Evidence map›Paper›PMID 31392398›Full record

ArticleLung2019

Growth Hormone-Releasing Hormone Receptor Antagonist Modulates Lung Inflammation and Fibrosis due to Bleomycin.

Chongxu Zhang, Renzhi Cai, Aaron Lazerson, Gaetan Delcroix, Medhi Wangpaichitr, Mehdi Mirsaeidi, Anthony J Griswold, Andrew V Schally, Robert M Jackson

Open access · hybridAbstract read
In one paragraph

Article in Lung, 2019. 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
4.5field-weighted citation impact, top 5% 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, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Growth hormone - releasing hormone in the immune system.Reviews in endocrine & metabolic disorders · 2025
    Review
  4. Review
  5. Growth hormone-releasing hormone and cancer.Reviews in endocrine & metabolic disorders · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Alleviation of LPS-induced Endothelial Injury due to GHRH Antagonist Treatment.International journal of peptide research and therapeutics · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Growth Hormone and the Human Hair Follicle.International journal of molecular sciences · 2021
    Review
  18. Article
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Chongxu ZhangResearch Service, Miami VAHS, Miami, FL, 33125, USA.
Renzhi CaiResearch Service, Miami VAHS, Miami, FL, 33125, USA.
Aaron LazersonDepartment of Comparative Pathology, University of Miami, Miami, FL, 33101, USA.
Gaetan DelcroixResearch Service, Miami VAHS, Miami, FL, 33125, USA.
Medhi WangpaichitrResearch Service, Miami VAHS, Miami, FL, 33125, USA.
Mehdi MirsaeidiResearch Service, Miami VAHS, Miami, FL, 33125, USA.
Anthony J GriswoldDr. John T. MacDonald Foundation Department of Human Genetics, University of Miami, Miami, FL, 33101, USA.
Andrew V SchallyResearch Service, Miami VAHS, Miami, FL, 33125, USA.
Robert M JacksonResearch Service, Miami VAHS, Miami, FL, 33125, USA. rjackson2@med.miami.edu.ORCID 0000-0001-5892-1193
University of Miami · USMiami VA Healthcare System · US

Funding

BLRD VA I01 BX004371BLRD VA I01 BX005051
6 · The paper itself

Abstract

purposeGrowth hormone-releasing hormone (GHRH) is a 44-amino acid peptide that regulates growth hormone (GH) secretion. We hypothesized that a GHRH receptor (GHRH-R) antagonist, MIA-602, would inhibit bleomycin-induced lung inflammation and/or fibrosis in C57Bl/6J mice.

methodsWe tested whether MIA-602 (5 μg or vehicle given subcutaneously [SC] on days 1-21) would decrease lung inflammation (at day 14) and/or fibrosis (at day 28) in mice treated with intraperitoneal (IP) bleomycin (0.8 units on days 1, 3, 7, 10, 14, and 21). Bleomycin resulted in inflammation and fibrosis around airways and vessels evident histologically at days 14 and 28.

resultsInflammation (histopathologic scores assessed blindly) was visibly less evident in mice treated with MIA-602 for 14 days. After 28 days, lung hydroxyproline (HP) content increased significantly in mice treated with vehicle; in contrast, lung HP did not increase significantly compared to naïve controls in mice treated with GHRH-R antagonist. GHRH-R antagonist increased basal and maximal oxygen consumption of cultured lung fibroblasts. Multiple genes related to chemotaxis, IL-1, chemokines, regulation of inflammation, and extracellular signal-regulated kinases (ERK) were upregulated in lungs of mice treated with bleomycin and MIA-602. MIA-602 also prominently suppressed multiple genes related to the cellular immune response including those for T-cell differentiation, receptor signaling, activation, and cytokine production.

conclusionsMIA-602 reduced lung inflammation and fibrosis due to bleomycin. Multiple genes related to immune response and T-cell functions were downregulated, supporting the view that MIA-602 can modulate the cellular immune response to bleomycin lung injury.

Indexed as

BleomycinAnimalsCells, CulturedCytoprotectionDisease Models, AnimalExtracellular Signal-Regulated MAP KinasesFibroblastsGene Expression RegulationGrowth Hormone-Releasing HormoneHormone AntagonistsHydroxyprolineInflammation MediatorsLungMaleMice, Inbred C57BLPneumoniaBleomycinExtracellular Signal-Regulated MAP KinasesGHRH(1-29)NH2, (PhAc-Ada)(0)-Tyr(1), Arg(2), Fpa(5,6), Ala(8), Har(9), Tyr(Me)(10), His(11), Orn(12,) Abu(15), His(20), Orn(21), Nle(27), Arg(28), Har(29)-Growth Hormone-Releasing HormoneHormone AntagonistsHydroxyprolineInflammation MediatorsSermorelinBleomycinGrowth hormone-releasing hormoneIdiopathic pulmonary fibrosisMIA-602

Identifiers

PMID31392398
PMCPMC6778540
OpenAlexW2964807003

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.