Evidence map›Paper›PMID 39737035›Full record

ArticleOpen veterinary journal2024

Effect of

Nurmawati Fatimah, Sri Agus Sudjarwo, Arifa Mustika, Suharjono Suharjono, Jusak Nugraha, Hari Basuki Notobroto, Rochmah Kurnijasanti, Reny I'tishom, Wibi Riawan, Alphania Rahniayu

Abstract read
In one paragraph

Article in Open veterinary journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Nurmawati FatimahDoctoral Program of Medical Science, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
Sri Agus SudjarwoFaculty of Veterinary Medicine, Universitas Airlangga, Surabaya, Indonesia.
Arifa MustikaDepartment of Anatomy, Histology and Pharmacology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
Suharjono SuharjonoDepartment of Pharmacy Practice, Faculty of Pharmacy, Universitas Airlangga, Surabaya, Indonesia.
Jusak NugrahaDepartment of Clinical Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
Hari Basuki NotobrotoDepartment Biostatistics, Faculty of Public Health Airlangga University, Surabaya, Indonesia.
Rochmah KurnijasantiFaculty of Veterinary Medicine, Universitas Airlangga, Surabaya, Indonesia.
Reny I'tishomDepartment of Medical Biology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
Wibi RiawanDepartment of Biochemistry and Biology Molecular, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
Alphania RahniayuDepartment of Anatomical Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hyperglycemia is a condition in which blood sugar levels increase excessively due to a variety of factors, one of which is the body's inability to regulate insulin properly. Diabetes closely relates to this condition, which significantly contributes to premature death and disability. Long-term diabetes treatment accompanied by a strict diet provides real results in controlling blood glucose levels but can cause side effects. Therefore, it is necessary to conduct research on the potential for new drug sources with minimal side effects. Traditional medicine empirically uses the plant Aim: This study was conducted to determine the effect of Methods: The experimental animals were divided into 5 groups: 1 normal group, 1 group induced with Streptozotocin (STZ) 50 mg/kgBW to treat hyperglycemia, and 3 other groups induced with STZ 50 mg/kgBW and given 70% ethanol extract of Results: It was found that giving STZ to rat can cause hyperglycemia. This was shown by measuring fasting blood glucose in rat and then measuring Bcl2 as an antiapoptotic agent. Bcl2 levels rose compared to the hyperglycemic control group and can lower apoptosis expression in heart cells of hyperglycemic model rat with an optimal dose of 90 mg/kgBW. In addition, the results showed that isoarborinol acetate and myricitrin compounds have inhibition of alpha-glucosidase and caspase-3. Conclusion: It can be concluded that EEPa is one of the alternative choices to overcome hyperglycemia.

Indexed as

ApoptosisCaspase InhibitorsFlavonoidsGlycoside Hydrolase InhibitorsHyperglycemiaPhytolaccaceaePlant ExtractsPlant LeavesTriterpenesalpha-GlucosidasesAnimalsBlood GlucoseCaspase 3Disease Models, AnimalMaleMyocytes, Cardiac3-hydroxydiploptenealpha-GlucosidasesBcl2 protein, ratBlood GlucoseCaspase 3Caspase InhibitorsFlavonoidsGlycoside Hydrolase InhibitorsmyricitrinPlant ExtractsProto-Oncogene Proteins c-bcl-2StreptozocinTriterpenesApoptosisBcl2DiabetesHyperglycemiaPetiveria alliacea

Identifiers

PMID39737035
PMCPMC11682742

What OpenQuestion holds

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LicenceCC BY-NC
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.