ArticleProtoplasma2026
Exploring the dual benefits: acute and subacute toxicity, hypolipidemic, slimming and hypoglycemic effects of Moringa oleifera lam : Leaf extract in female wistar albino rats.
Article in Protoplasma, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Moringa oleifera (MO) from the Ghardaia region (southern Algeria) is traditionally used to manage metabolic disorders. This study evaluates the biochemical and histological effects MO hydro-methanolic leaf extract (MHE) following toxicological assessment in rats to provide safety data supporting its use as a slimming, hypolipidemic and hypoglycemic nutraceutical. For this, an acute toxicity study was assessed following Guideline 425 of OECD, using doses of 4000 and 6000 mg/kg, while a sub-acute toxicity study was evaluated according to Guideline 407 of OECD, involving daily oral administration of 400, 700, and 1000 mg/kg to female Wistar Albino rats (FWA) for 7 and 28 days, respectively. Following the treatment period, the rats were sacrificed for biochemical and histological analyses in accordance with standard protocols. As a result, no mortality or overt toxicity was observed, indicating a lethal dose (LD50) exceeding 6000 mg/kg (Acute) and 1000 mg/kg (Sub-acute). Following single-dose administration, liver relative weight increased alongside elevated transaminase levels indicating hepatocellular necrosis. In contrast, repeated dosing led to reductions in weight gain, glucose levels, improved lipid profile, and lowered transaminases without signs of liver damage. Histology revealed inflammatory infiltration in the renal glomeruli and reversible destruction of intestinal villi and glands in all treated groups. We can conclude that the extract shows promise for managing metabolic disorders but poses potential toxicity risks at repeated doses exceeding 400 mg/kg.
Indexed as
Identifiers
41826532What OpenQuestion holds
Registered trials
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.