Evidence map›Paper›PMID 37242459›Full record

ReviewPharmaceuticals (Basel, Switzerland)2023

Stable Gastric Pentadecapeptide BPC 157 May Recover Brain-Gut Axis and Gut-Brain Axis Function.

Predrag Sikiric, Slaven Gojkovic, Ivan Krezic, Ivan Maria Smoday, Luka Kalogjera, Helena Zizek, Katarina Oroz, Hrvoje Vranes, Vlasta Vukovic, May Labidi and 14 more

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2023. 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
2.3field-weighted citation impact, top 12% 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, 13 citations in OpenAlex.

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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

24 authors at 3 institutions in 1 country.

Predrag SikiricDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Slaven GojkovicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0003-4020-326X
Ivan KrezicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Ivan Maria SmodayDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Luka KalogjeraDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0002-1703-0033
Helena ZizekDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Katarina OrozDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Hrvoje VranesDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0003-3544-8385
Vlasta VukovicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
May LabidiDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Sanja StrbeDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Lidija Baketic OreskovicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Marko SeverDepartment of Surgery, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Marijan TepesDepartment of Clinical Medicine, Faculty of Dental Medicine and Health, University of Osijek, 31000 Osijek, Croatia.
Mario KnezevicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Ivan BarisicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Vladimir BlagaicDepartment of Obstetrics and Gynecology, Clinical Hospital Sveti Duh, 10000 Zagreb, Croatia.
Josipa VlainicLaboratory for Advanced Genomics, Division of Molecular Medicine, lnstitute Ruder Boskovic, 10000 Zagreb, Croatia.
Ivan DobricDepartment of Surgery, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Mario StaresinicDepartment of Surgery, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Anita SkrticDepartment of Pathology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0002-9275-7283
Ivana JurjevicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Alenka Boban BlagaicDepartment of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Sven SeiwerthDepartment of Pathology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
University of Zagreb · HRRuđer Bošković Institute · HRUniversity of Osijek · HR

Funding

University of Zagreb 099
6 · The paper itself

Abstract

Conceptually, a wide beneficial effect, both peripherally and centrally, might have been essential for the harmony of brain-gut and gut-brain axes' function. Seen from the original viewpoint of the gut peptides' significance and brain relation, the favorable stable gastric pentadecapeptide BPC 157 evidence in the brain-gut and gut-brain axes' function might have been presented as a particular interconnected network. These were the behavioral findings (interaction with main systems, anxiolytic, anticonvulsive, antidepressant effect, counteracted catalepsy, and positive and negative schizophrenia symptoms models). Muscle healing and function recovery appeared as the therapeutic effects of BPC 157 on the various muscle disabilities of a multitude of causes, both peripheral and central. Heart failure was counteracted (including arrhythmias and thrombosis), and smooth muscle function recovered. These existed as a multimodal muscle axis impact on muscle function and healing as a function of the brain-gut axis and gut-brain axis as whole. Finally, encephalopathies, acting simultaneously in both the periphery and central nervous system, BPC 157 counteracted stomach and liver lesions and various encephalopathies in NSAIDs and insulin rats. BPC 157 therapy by rapidly activated collateral pathways counteracted the vascular and multiorgan failure concomitant to major vessel occlusion and, similar to noxious procedures, reversed initiated multicausal noxious circuit of the occlusion/occlusion-like syndrome. Severe intracranial (superior sagittal sinus) hypertension, portal and caval hypertensions, and aortal hypotension were attenuated/eliminated. Counteracted were the severe lesions in the brain, lungs, liver, kidney, and gastrointestinal tract. In particular, progressing thrombosis, both peripherally and centrally, and heart arrhythmias and infarction that would consistently occur were fully counteracted and/or almost annihilated. To conclude, we suggest further BPC 157 therapy applications.

Indexed as

brain–gut axisencephalopathygastric pentadecapeptide BPC 157gut–brain axisheart failuremuscleocclusion-like syndromeocclusion syndrome

Identifiers

PMID37242459
PMCPMC10224484
OpenAlexW4367626429

What OpenQuestion holds

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LicenceCC BY
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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.