Evidence map›Paper›PMID 38980576›Full record

ReviewInflammopharmacology2024

New studies with stable gastric pentadecapeptide protecting gastrointestinal tract. significance of counteraction of vascular and multiorgan failure of occlusion/occlusion-like syndrome in cytoprotection/organoprotection.

Predrag Sikiric, Marko Sever, Ivan Krezic, Hrvoje Vranes, Luka Kalogjera, Ivan Maria Smoday, Vlasta Vukovic, Katarina Oroz, Luka Coric, Marija Skoro and 12 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Inflammopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

22 authors.

Predrag SikiricDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia. sikiric@mef.hr.ORCID http://orcid.org/0000-0002-7952-2252
Marko SeverDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Ivan KrezicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Hrvoje VranesDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Luka KalogjeraDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Ivan Maria SmodayDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Vlasta VukovicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Katarina OrozDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Luka CoricDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Marija SkoroDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Ivana KaveljDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Slavica ZubcicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Suncana SikiricDepartment of Pathology, School of Medicine, University of Zagreb, 10000, Zagreb, Croatia.
Lidija Beketic OreskovicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Ivana OreskovicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Vladimir BlagaicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Klara BrcicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Sanja StrbeDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Mario StaresinicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Alenka Boban BlagaicDepartment of Pharmacology, School of Medicine, University of Zagreb, Zagreb, Croatia.
Anita SkrticDepartment of Pathology, School of Medicine, University of Zagreb, 10000, Zagreb, Croatia.
Sven SeiwerthDepartment of Pathology, School of Medicine, University of Zagreb, 10000, Zagreb, Croatia.

Funding

Sveučilište u Zagrebu 10106-22-3071
6 · The paper itself

Abstract

Since the early 1990s, when Robert's and Szabo's cytoprotection concept had already been more than one decade old, but still not implemented in therapy, we suggest the stable gastric pentadecapeptide BPC 157 as the most relevant mediator of the cytoprotection concept. Consequently, it can translate stomach and gastrointestinal mucosal maintenance, epithelium, and endothelium cell protection to the therapy of other tissue healing (organoprotection), easily applicable, as native and stable in human gastric juice for more than 24 h. These overwhelm current clinical evidence (i.e., ulcerative colitis, phase II, no side effects, and no lethal dose (LD1) in toxicology studies), as BPC 157 therapy effectively combined various tissue healing and lesions counteraction. BPC 157 cytoprotection relevance and vascular recovery, activation of collateral pathways, membrane stabilizer, eye therapy, wound healing capability, brain-gut and gut-brain functioning, tumor cachexia counteraction, muscle, tendon, ligament, and bone disturbances counteraction, and the heart disturbances, myocardial infarction, heart failure, pulmonary hypertension, arrhythmias, and thrombosis counteraction appeared in the recent reviews. Here, as concept resolution, we review the counteraction of advanced Virchow triad circumstances by activation of the collateral rescuing pathways, depending on injury, activated azygos vein direct blood flow delivery, to counteract occlusion/occlusion-like syndromes starting with the context of alcohol-stomach lesions. Counteraction of major vessel failure (congested inferior caval vein and superior mesenteric vein, collapsed azygos vein, collapsed abdominal aorta) includes counteraction of the brain (intracerebral and intraventricular hemorrhage), heart (congestion, severe arrhythmias), lung (hemorrhage), and congestion and lesions in the liver, kidney, and gastrointestinal tract, intracranial (superior sagittal sinus), portal and caval hypertension, aortal hypotension, and thrombosis, peripherally and centrally.

Indexed as

CytoprotectionGastrointestinal TractMultiple Organ FailurePeptide FragmentsProtective AgentsAnimalsArterial Occlusive DiseasesBrain-Gut AxisDisease Models, AnimalHumansProteinsVenous ThrombosisBPC 157Peptide FragmentsProtective AgentsProteinsCytoprotectionOcclusion/occlusion-like syndromesOrganoprotectionSelye’s stress responseStable gastric pentadecapeptide BPC 157TherapyVascular recovery

Identifiers

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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.