Evidence map›Paper›PMID 36077579›Full record

ArticleInternational journal of molecular sciences2022

Systemic Beta-Hydroxybutyrate Affects BDNF and Autophagy into the Retina of Diabetic Mice.

Maria Consiglia Trotta, Carlo Gesualdo, Hildegard Herman, Sami Gharbia, Cornel Balta, Caterina Claudia Lepre, Marina Russo, Annalisa Itro, Giovanbattista D'Amico, Luisa Peluso and 7 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 21 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

17 authors at 2 institutions in 2 countries.

Maria Consiglia TrottaDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via Santa Maria di Costantinopoli 16, 80138 Naples, Italy.ORCID 0000-0001-9813-5955
Carlo GesualdoEye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania "Luigi Vanvitelli", Via Luigi de Crecchio 6, 80138 Naples, Italy.
Hildegard Herman"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 86 Revolutiei Av., 310414 Arad, Romania.ORCID 0000-0002-6741-0245
Sami Gharbia"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 86 Revolutiei Av., 310414 Arad, Romania.
Cornel Balta"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 86 Revolutiei Av., 310414 Arad, Romania.ORCID 0000-0001-5734-0071
Caterina Claudia LepreDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via Santa Maria di Costantinopoli 16, 80138 Naples, Italy.
Marina RussoDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via Santa Maria di Costantinopoli 16, 80138 Naples, Italy.
Annalisa ItroPhD Course in Translational Medicine (XXXV Cycle), Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via Santa Maria di Costantinopoli 16, 80138 Naples, Italy.ORCID 0000-0002-0226-7521
Giovanbattista D'AmicoDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via Santa Maria di Costantinopoli 16, 80138 Naples, Italy.
Luisa PelusoDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via Santa Maria di Costantinopoli 16, 80138 Naples, Italy.
Iacopo PanareseDepartment of Mental and Physical Health and Preventive Medicine, University of Campania "Luigi Vanvitelli", Largo Madonna Delle Grazie 1, 80138 Naples, Italy.
Gorizio PierettiEye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania "Luigi Vanvitelli", Via Luigi de Crecchio 6, 80138 Naples, Italy.
Giuseppe FerraroEye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania "Luigi Vanvitelli", Via Luigi de Crecchio 6, 80138 Naples, Italy.
Francesca SimonelliEye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania "Luigi Vanvitelli", Via Luigi de Crecchio 6, 80138 Naples, Italy.
Michele D'AmicoDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via Santa Maria di Costantinopoli 16, 80138 Naples, Italy.ORCID 0000-0002-6899-0595
Settimio RossiEye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania "Luigi Vanvitelli", Via Luigi de Crecchio 6, 80138 Naples, Italy.
Anca Hermenean"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 86 Revolutiei Av., 310414 Arad, Romania.ORCID 0000-0001-8510-6653
University of Campania "Luigi Vanvitelli" · ITVasile Goldis Western University of Arad · RO

Funding

Italian Ministry of Education, University and Research PRIN 2020FR7TCL_002
6 · The paper itself

Abstract

Background: Diabetic retinopathy (DR) is a neurovascular disease, characterized by a deficiency of brain-derived neurotrophic factor (BDNF), a regulator of autophagy. Beta-hydroxybutyrate (BHB), previously reported as a protective agent in DR, has been associated with BDNF promotion. Here, we investigated whether systemic BHB affects the retinal levels of BDNF and local autophagy in diabetic mice with retinopathy; Methods: C57BL/6J mice were administered with intraperitoneal (i.p.) streptozotocin (STZ) (75 mg/kg) injection to develop diabetes. After 2 weeks, they received i.p. injections of BHB (25−50−100 mg/kg) twice a week for 10 weeks. Retinal samples were collected in order to perform immunofluorescence, Western blotting, and ELISA analysis; Results: BHB 50 mg/kg and 100 mg/kg significantly improved retinal BDNF levels (p < 0.01) in diabetic mice. This improvement was negatively associated with autophagosome−lysosome formations (marked by LC3B and ATG14) and to higher levels of connexin 43 (p < 0.01), a marker of cell integrity. Moreover, BHB administration significantly reduced M1 microglial activation and autophagy (p < 0.01); Conclusions: The systemic administration of BHB in mice with DR improves the retinal levels of BDNF, with the consequent reduction of the abnormal microglial autophagy. This leads to retinal cell safety through connexin 43 restoration.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic Retinopathy3-Hydroxybutyric AcidAnimalsAutophagyBrain-Derived Neurotrophic FactorConnexin 43MiceMice, Inbred C57BLRetina3-Hydroxybutyric AcidBrain-Derived Neurotrophic FactorConnexin 43autophagybeta-hydroxybutyratebrain-derived neurotrophic factordiabetic retinopathyhydroxycarboxylic acid receptor 2microglia

Identifiers

PMID36077579
PMCPMC9455989
OpenAlexW4294733827

What OpenQuestion holds

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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.