Evidence map›Paper›PMID 33456981›Full record

ArticleActa naturae

A Simplified Streptozotocin-Induced Diabetes Model in Nude Mice.

I G Gvazava, A V Kosykh, O S Rogovaya, O P Popova, K A Sobyanin, A C Khrushchev, A V Timofeev, E A Vorotelyak

Open access · diamondAbstract read
In one paragraph

Article in Acta naturae. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Modified streptozotocin-induced diabetic model in rodents.Animal models and experimental medicine · 2024
    Article
  6. Effect ofInternational journal of molecular sciences · 2023
    Article
  7. Article
  8. Review
  9. 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.

I G GvazavaKoltsov Institute of Developmental Biology, Russian Academy of Sciences, Moscow, 119334 Russia.
A V KosykhKoltsov Institute of Developmental Biology, Russian Academy of Sciences, Moscow, 119334 Russia.
O S RogovayaKoltsov Institute of Developmental Biology, Russian Academy of Sciences, Moscow, 119334 Russia.
O P PopovaNational Medical Research Treatment and Rehabilitation Centre, Ministry of Health of the Russian Federation, Moscow, 125367 Russia.
K A SobyaninPirogov Russian National Research Medical University, Ministry of Health of the Russian Federation, Moscow, 117997 Russia.
A C KhrushchevPirogov Russian National Research Medical University, Ministry of Health of the Russian Federation, Moscow, 117997 Russia.
A V TimofeevPirogov Russian National Research Medical University, Ministry of Health of the Russian Federation, Moscow, 117997 Russia.
E A VorotelyakKoltsov Institute of Developmental Biology, Russian Academy of Sciences, Moscow, 119334 Russia.
Ministry of Health of the Russian Federation · RUPirogov Russian National Research Medical University · RUKoltzov Institute of Developmental Biology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preclinical studies of human cellular and tissue-based products (HCT/Ps) for transplantation therapy of type 1 diabetes mellitus (T1DM) necessarily involve animal models, particularly mouse models of diabetes induced by streptozotocin (STZ). These models should mimic the clinical and metabolic manifestations of T1DM in humans (face validity) and be similar to T1DM in terms of the pathogenetic mechanism (construct validity). Furthermore, since HCT/Ps contain human cells, modeling of diabetes in immune-deficient animals is obligatory. Here we describe the most simplified diabetes model in Nude mice. Diabetes was induced in 31 males by a single intraperitoneal injection of STZ in normal saline at a medium-to-high dose of 150 mg/kg body weight. Fourteen control animals received only saline. Non-fasting plasma glucose (PG) levels were measured periodically for 50 days. All STZ-treated mice survived beyond 50 days. By day 15 after STZ administration, 22 of 31 (71%) mice developed stable diabetes based on the following criteria: (1) non-fasting PG ≥ 15 mmol/L on consecutive measurements up until day 50; (2) no diabetes remission. The mean non-fasting PG in mice with stable diabetes over the period of 35 days was equal to 25.7 mmol/L. On day 50, mean plasma insulin concentration, mean pancreatic insulin content, and the average number of β-cells in pancreatic islets were 2.6, 8.4, and 50 times lower, respectively, than in the control animals. We consider that our Nude mouse model of diabetes meets face validity and construct validity criteria and can be used in preclinical studies of HCT/Ps.

Indexed as

animal modeldiabetes mellitusNude micestreptozotocin

Identifiers

PMID33456981
PMCPMC7800597
OpenAlexW3121629685

What OpenQuestion holds

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LicenceCC BY
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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.