Evidence map›Paper›PMID 36430204›Full record

ArticleInternational journal of molecular sciences2022

Contrast-Free FLIM Reveals Metabolic Changes in Pathological Islets of Langerhans.

Polina Ermakova, Alena Kashirina, Irina Kornilova, Aleksandra Bogomolova, Darya Myalik, Nasipbek Naraliev, Denis Kuchin, Liya Lugovaya, Elena Zagaynova, Vladimir Zagainov and 1 more

Abstract 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. A Fresh Look at Islet Isolation from Rabbit Pancreases.International journal of molecular sciences · 2024
    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

11 authors.

Polina ErmakovaInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.ORCID 0000-0002-5671-3216
Alena KashirinaInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.ORCID 0000-0001-6827-8787
Irina KornilovaInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.ORCID 0000-0001-6981-4449
Aleksandra BogomolovaInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.
Darya MyalikInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.
Nasipbek NaralievInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.
Denis KuchinInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.
Liya LugovayaInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.
Elena ZagaynovaInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.
Vladimir ZagainovInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.
Aleksandra KashinaInstitute of Experimental Oncology and Biomedical Technologies, Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Pl., 603005 Nizhny Novgorod, Russia.

Funding

Ministry of Health of the Russian Federation State task АААА-А20-120022590096-6 on the topic "Creation of technology encapsulation of pancreatic islets to compensate for absolute insulin-deficient conditions"
6 · The paper itself

Abstract

FLIM (Fluorescence Lifetime Imaging Microscopy) is a powerful tool that could be used in the future to diagnose islet cell recovery after therapy. The identification of appropriate FLIM parameters is required to determine islet quality and islet cell metabolism throughout the organ under various conditions of insulin deficiency. The aim of the work was to identify key FLIM parameters, changes of which are characteristic of pancreatic pathologies. The τm, τ1, τ2, α1, α2 and α1/α2 of free and bound forms of NAD(P)H of the islet cells of animals (rats and pigs) and of humans with and without pathologies were measured and analyzed. The data were confirmed by IHC and histological studies. We identified three FLIM parameters in islet cells from animals with streptozotocin (STZ)-induced diabetes mellitus (DM) and from humans with chronic pancreatitis + type 2 diabetes (T2D), which differ in the same way: τm and α2 take lower values compared to the nonpathological islet cells, while α1/α2 takes higher values. In islet cells from patients with adenocarcinoma (PDAC) and chronic pancreatitis, these parameters had reverse tendency relative to the norm or did not differ. Thus, minimally invasive and non-contrast FLIM methods may, in the future, be used to diagnose pathological islet cells.

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Islets of LangerhansPancreatitis, ChronicAnimalsHumansInsulinNADRatsSwineInsulinNADdiabetesFLIMfluorescence lifetimesinsulin-deficient conditionsislets cellsNAD(P)H

Identifiers

PMID36430204
PMCPMC9698393

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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.