Evidence map›Paper›PMID 29402248›Full record

ArticleBMC complementary and alternative medicine2018

Acute and sub-acute oral toxicity of Dracaena cinnabari resin methanol extract in rats.

Nashwan Abdullah Al-Afifi, Aied Mohammed Alabsi, Marina Mohd Bakri, Anand Ramanathan

Abstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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  15. Acute toxicity of aqueous extract ofToxicological research · 2022
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  16. Silibinin Schiff Base Derivatives Counteract CClDrug design, development and therapy · 2022
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  17. Evidence-based complementary and alternative medicine : eCAM · 2022
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  18. Article
  19. Molecules (Basel, Switzerland) · 2021
    Article
  20. A 90-Day Oral Toxicity Study of an Ethanolic Root Extract ofEvidence-based complementary and alternative medicine : eCAM · 2021
    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

4 authors.

Nashwan Abdullah Al-AfifiDepartment of Oral and Craniofacial Sciences, Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Aied Mohammed AlabsiDepartment of Oral Biology and Biomedical Sciences, Faculty of Dentistry, MAHSA University, 42610, Jenjarom, Selangor, Malaysia. aied_absi@yahoo.com.
Marina Mohd BakriDepartment of Oral and Craniofacial Sciences, Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Anand RamanathanDepartment of Oral & Maxillofacial Clinical Sciences, Faculty of Dentistry, University of Malaya, Kuala Lumpur, 50603, Malaysia.

Funding

Ministry of Higher Education, Malaysia (MY) UM.C/625/1/HIR/MoE/DENT /24Universiti Malaya RG422/12HTM
6 · The paper itself

Abstract

backgroundDracaena cinnabari (DC) is a perennial tree that located on the Southern coast of Yemen native to the Socotra Island. This tree produces a deep red resin known as the Dragon's blood, the Twobrother's Blood or Damm Alakhwain. The current study performed to evaluate the safety of the DC resin methanol extract after a single or 28 consecutive daily oral administrations.

methodsIn assessing the safety of DC resin methanol extract, acute and sub-acute oral toxicity tests performed following OECD guidelines 423 and 407, respectively, with slight modifications. In acute oral toxicity test, DC resin methanol extract administered to female Sprague Dawley rats by oral gavage at a single dose of 300 and 2000 mg/kg body weight. Rats observed for toxic signs for 14 days. In sub-acute oral toxicity test, DC resin methanol extract administered to the rats by oral gavage at 500, 1000, and 1500 mg/kg body weight daily up to 28 days to male and female Spradgue Dawley rats. The control and high dose in satellite groups were also maintained and handled as the previous groups to determine the late onset toxicity of DC resin methanol extract. At the end of each test, hematological and biochemical analysis of the collected blood were performed as well as gross and microscopic pathology.

resultsIn acute oral toxicity, no treatment-related death or toxic signs were observed. It revealed that the DC resin methanol extract could be well tolerated up to the dose 2000 mg/kg body weight and could be classified as Category 5. The sub-acute test observations indicated that there are no treatment-related changes up to the high dose level compared to the control. Food consumption, body weight, organ weight, hematological parameters, biochemical parameters and histopathological examination (liver, kidney, heart, spleen and lung) revealed no abnormalities. Water intake was significantly higher in the DC resin methanol extract treated groups compared to the control.

conclusionThis study demonstrates tolerability of DC resin methanol extract administered daily for 28 days up to 1500 mg/kg dose.

Indexed as

Administration, OralAnimalsBody WeightDracaenaDrinkingEatingFemaleHeartKidneyMaleMethanolOrgan SizeRatsRats, Sprague-DawleyResins, PlantToxicity Tests, AcuteMethanolResins, PlantAcute oral toxicityBiochemical parametersDC resin methanol extractHematological parametersHistopathologySub-acute oral toxicity

Identifiers

PMID29402248
PMCPMC5800047

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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.