Evidence map›Paper›PMID 37423995›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Assessment of Kidney Mitochondrial Function by High-Resolution Respirometry, Transmission Electron Microscopy, and Histological Techniques.

Marisol Orozco-Ibarra, Omar Emiliano Aparicio-Trejo, Alexis Paulina Jiménez-Uribe, Estefani Yaquelin Hernández-Cruz, Ana Karina Aranda-Rivera, Isabel Amador-Martínez, Francisca Fernández-Valverde, José Pedraza-Chaverri

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 3 institutions in 1 country.

Marisol Orozco-Ibarra *Departamento de Bioquímica, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Omar Emiliano Aparicio-Trejo *Departamento de Fisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Alexis Paulina Jiménez-UribeFacultad de Química, Departamento de Biología, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Estefani Yaquelin Hernández-CruzFacultad de Química, Departamento de Biología, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Ana Karina Aranda-RiveraFacultad de Química, Departamento de Biología, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Isabel Amador-MartínezFacultad de Química, Departamento de Biología, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Francisca Fernández-ValverdeLaboratorio de Patología Experimental, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
José Pedraza-ChaverriFacultad de Química, Departamento de Biología, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico. pedraza@unam.mx.
Universidad Nacional Autónoma de México · MXInstituto Nacional de Cardiología · MXInstituto Nacional de Neurología y Neurocirugía · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proper kidney function depends highly on mitochondria homeostasis. This organelle is the primary source of ATP production in the kidney and regulates other cellular processes such as redox and calcium homeostasis. Although the mitochondria's primary recognized function is cellular energy production, through the function of the Krebs cycle, electron transport system (ETS), as well as oxygen and electrochemical gradient consumption, this function is interconnected with multiple signaling and metabolic pathways, making bioenergetics a central hub in renal metabolism. Furthermore, mitochondrial biogenesis, dynamics, and mass are also strongly related to bioenergetics. This central role is not surprising given that mitochondrial impairment, including functional and structural alterations, has been recently reported in several kidney diseases. Here, we describe assessment of mitochondrial mass, structure, and bioenergetics in kidney tissue and renal-derived cell lines. These methods allow investigation of mitochondrial alterations in kidney tissue and renal cells under different experimental conditions.

Indexed as

Energy MetabolismMitochondriaHistological TechniquesKidneyMicroscopy, Electron, TransmissionEnzyme histochemistryKidney histologyMitochondrial bioenergeticsMitochondrial mass

Identifiers

PMID37423995
OpenAlexW4383711221

What OpenQuestion holds

Textmetadata
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.