Evidence map›Paper›PMID 30170600›Full record

ArticleLipids in health and disease2018

Comparative study on the independent and combined effects of omega-3 and vitamin B12 on phospholipids and phospholipase A2 as phospholipid hydrolyzing enzymes in PPA-treated rats as a model for autistic traits.

Hanan Alfawaz, Ramesa Shafi Bhat, Manar Al-Mutairi, Osima M Alnakhli, Abeer Al-Dbass, Mona AlOnazi, Majidh Al-Mrshoud, Iman H Hasan, Afaf El-Ansary

Open access · goldAbstract read
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Article in Lipids in health and disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 12 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

9 authors at 3 institutions in 1 country.

Hanan AlfawazDepartment of Food Science and Nutrition, College of Food and Agriculture Sciences, King Saud University, P.O. Box 22452, Riyadh, Saudi Arabia.
Ramesa Shafi BhatBiochemistry Department, College of Science, King Saud University, Riyadh, 11451, Kingdom of Saudi Arabia.
Manar Al-MutairiCentral Laboratory, Center for Female Scientific and Medical Colleges, King Saud University, Riyadh, Saudi Arabia.
Osima M AlnakhliCentral Laboratory, Center for Female Scientific and Medical Colleges, King Saud University, Riyadh, Saudi Arabia.
Abeer Al-DbassBiochemistry Department, College of Science, King Saud University, Riyadh, 11451, Kingdom of Saudi Arabia.
Mona AlOnaziBiochemistry Department, College of Science, King Saud University, Riyadh, 11451, Kingdom of Saudi Arabia.
Majidh Al-MrshoudCentral Laboratory, Center for Female Scientific and Medical Colleges, King Saud University, Riyadh, Saudi Arabia.
Iman H HasanPharmacology and Toxicology Department, College of Pharmacy, Riyadh, Saudi Arabia.
Afaf El-AnsaryCentral Laboratory, Center for Female Scientific and Medical Colleges, King Saud University, Riyadh, Saudi Arabia. afafkelansary@gmail.com.ORCID http://orcid.org/0000-0002-1404-5248
King Saud University · SAKing Saud Medical City · SARiyadh Elm University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAbnormal phospholipid metabolism is a major component of many neurodevelopmental disorders including autism. Oral administration of propionic acid (PPA) can produce behavioral abnormalities and biochemical features in rodents similar to those observed in autism and can thus be used as a model to understand impaired brain fatty acid metabolism in autism.

methodsThe present study was designed to understand alterations in phospholipid metabolism in the brain of a rodent model of autism and to explore omega-3 and vitamin B12 as remedies. Five groups of rats were selected: Group 1 was the control. Group 2 was the rodent model of autism treated with a neurotoxic dose of PPA. Group 3 was given vitamin B12 cobalamin (16.7 mg/kg/day) for 30 days after PPA treatment. Group 4 was given pharmaceutical grade Omega-3 (200 mg cholesterol free-DHA/kg body weight/day), a product of Madre lab, Germany, for 30 days after PPA treatment for 3 days. Group 5 was given a combined dose of ω-3 + Vitamin B12 for the same duration post-PPA treatment. Phospholipid levels and Phospholipase A2 were measured in the brain homogenates of all the groups. ELISA and western blotting were used to detect the cPLA2 protein level.

resultsA significant decrease in phospholipid levels and a significant increase in cPLA2 were found in brain tissue of PPA-treated rats; however, both ω-3 and vitamin B12 were efficient in ameliorating the neurotoxic effect of PPA.

conclusionBoth ω-3 and vitamin B12 may play a role in ameliorating impaired phospholipid metabolism in autism; however, proper clinical trials are needed.

Indexed as

AnimalsAutistic DisorderCholesterolDietary SupplementsDisease Models, AnimalFatty Acids, Omega-3HumansHydrolysisLipid MetabolismMalePhospholipases A2PhospholipidsPropionatesRatsVitamin B 12CholesterolFatty Acids, Omega-3Phospholipases A2PhospholipidsPropionatespropionic acidVitamin B 12AutismOmega-3Phospholipase A2PhospholipidsPropionic acidVitamin B12

Identifiers

PMID30170600
PMCPMC6119280
OpenAlexW2889130856

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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.