Evidence map›Paper›PMID 39903548›Full record

ArticleEndocrinology2025

Vasoinhibin is Generated by the Renin-angiotensin System.

Francisco Freinet Núñez, Lourdes Siqueiros-Marquez, Elva Adán-Castro, Magdalena Zamora, Juan Pablo Robles, Xarubet Ruíz-Herrera, Thomas Bertsch, Jakob Triebel, Gonzalo Martínez de la Escalera, Carmen Clapp

Abstract read
In one paragraph

Article in Endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Francisco Freinet NúñezInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.ORCID 0009-0004-1158-8441
Lourdes Siqueiros-MarquezInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.
Elva Adán-CastroInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.
Magdalena ZamoraInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.ORCID 0000-0001-5579-1004
Juan Pablo RoblesInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.ORCID 0000-0001-8429-1914
Xarubet Ruíz-HerreraInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.
Thomas BertschInstitute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, Nuremberg General Hospital and Paracelsus Medical University, 90419 Nuremberg, Germany.
Jakob TriebelInstitute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, Nuremberg General Hospital and Paracelsus Medical University, 90419 Nuremberg, Germany.ORCID 0000-0002-1989-8645
Gonzalo Martínez de la EscaleraInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.ORCID 0000-0002-4309-3476
Carmen ClappInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), 76230 Querétaro, México.ORCID 0000-0002-7670-6718

Funding

Consejo Nacional de Humanidades, Ciencia y Tecnología (CONAHCYT) 923115
6 · The paper itself

Abstract

Vasoinhibin is a fragment of the hormone prolactin (PRL) that inhibits angiogenesis, vasopermeability, and vasodilation. Cathepsin D (CTSD) cleaves the N-terminal of PRL to generate vasoinhibin in the retina of neonate mice as revealed by the CTSD inhibitor, pepstatin A. However, pepstatin A also inhibits renin. Because renin is expressed in the retina and the renin-angiotensin system gives rise to peptides with positive and negative effects on blood vessel growth and function, we investigated whether renin cleaves PRL to vasoinhibin in the newborn mouse retina and in the circulation. Newborn mouse retinal extracts from wild-type and CTSD-null newborn mice cleaved PRL to a 14 kDa vasoinhibin and such cleavage was prevented by heat-inactivation, pepstatin A, and the selective renin inhibitor VTP-27999 suggesting the contribution of renin. In agreement, recombinant renin cleaved different species PRLs to the expected 14-kDa vasoinhibin, a mass consistent with a consensus renin cleavage site located at Leu124-Leu125 in rat and mouse PRLs and at Leu126-Leu127 in human, bovine, and ovine PRLs. Dehydration followed by rehydration (D/R) in rats increased the levels of renin and PRL in plasma. Further increase in PRL circulating levels by the dopamine D2 receptor blocker, sulpiride, enabled detection of 14 kDa vasoinhibin in D/R rats. Moreover, the incubation of PRL with plasma from D/R rats generated a 14-kDa vasoinhibin that was prevented by VTP-27999. These findings add renin to the list of PRL-cleaving proteases and introduce vasoinhibin as a putative renin-angiotensin system-mediated mechanism for regulating blood vessel growth and function.

Indexed as

ProlactinRenin-Angiotensin SystemAnimalsAnimals, NewbornCell Cycle ProteinsHumansMaleMiceMice, KnockoutRatsReninRenin InhibitorsCell Cycle ProteinsProlactinReninRenin InhibitorsVASH1 protein, humancomparative endocrinologyprolactinreninrenin-angiotensin systemretinavasoinhibin

Identifiers

PMID39903548
PMCPMC11833480

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.