Evidence map›Paper›PMID 32356224›Full record

ArticleNatural products and bioprospecting2020

Genotoxicity and Safety Pharmacology Studies of Indole Alkaloids Extract from Leaves of Alstonia scholaris (L.) R. Br.

Yun-Li Zhao, Min Su, Jian-Hua Shang, Xia Wang, Guang-Lei Bao, Jia Ma, Qing-Di Sun, Fang Yuan, Jing-Kun Wang, Xiao-Dong Luo

Open access · diamondAbstract read
In one paragraph

Article in Natural products and bioprospecting, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. The safety and tolerability of alkaloids fromPharmaceutical biology · 2021
    Trial
  2. PeerJ · 2023
    Article
  3. Antinociceptive efficacy ofJournal of traditional and complementary medicine · 2023
    Article
  4. Article
  5. Safety assessment of HEA-enrichedFood science & nutrition · 2021
    Article
  6. Article
  7. Article
  8. Indole: The After Next Scaffold of Antiplasmodial Agents?Drug design, development and therapy · 2020
    Review
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 at 3 institutions in 1 country.

Yun-Li ZhaoState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, People's Republic of China.
Min SuYunnan Institute of Medical Material, Kunming, 650111, People's Republic of China.
Jian-Hua ShangYunnan Institute of Medical Material, Kunming, 650111, People's Republic of China.
Xia WangYunnan Institute of Medical Material, Kunming, 650111, People's Republic of China.
Guang-Lei BaoYunnan Institute of Medical Material, Kunming, 650111, People's Republic of China.
Jia MaYunnan Institute of Medical Material, Kunming, 650111, People's Republic of China.
Qing-Di SunJiangsu Nhwa Pharmaceutical Co., Ltd, Xuzhou, 221009, People's Republic of China.
Fang YuanYunnan Institute of Medical Material, Kunming, 650111, People's Republic of China.
Jing-Kun WangYunnan Institute of Medical Material, Kunming, 650111, People's Republic of China.
Xiao-Dong LuoState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, People's Republic of China. xdluo@mail.kib.ac.cn.
Yunnan University · CNJiangsu Nhwa Pharmaceutical (China) · CNKunming Institute of Botany · CN

Funding

National Basic Research Program of China (973 Program) (CN) 2017YFC1704007National Major Science and Technology Projects of China (CN) 2019FY003004National Major Science and Technology Projects of China (CN) 2019ZF003
6 · The paper itself

Abstract

Indole alkaloids extract (IAAS) was prepared from leaves of Alstonia scholaris (L.) R. Br., an evergreen tropical plant widely distributed throughout the world. This plant has been used historically by the Dai ethnic people of China to treat respiratory diseases. This study evaluated the genotoxicity and safety pharmacology of IAAS to support clinical use. The bacterial reverse mutation (Ames) test, in vitro mammalian chromosomal aberration test, and in vivo mammalian erythrocyte micronucleus (MN) test were performed to evaluate genotoxicity. Mice were administered IAAS (240, 480, or 960 mg/kg bw) once orally to observe adverse central nervous system effects. Furthermore, beagle dogs were administered IAAS (10, 30, 60 mg/kg bw) once via the duodenum to evaluate its effects on the cardiovascular and respiratory systems. IAAS with or without S9-induced metabolic activation showed no genotoxicity in the Ames test up to 500 μg/plate, in the mammalian chromosomal aberration test up to 710 μg/mL, or in the MN test up to 800 mg/kg bw. No abnormal neurobehavioral effects were observed in mice following treatment with up to 960 mg/kg bw of IAAS. Moreover, blood pressure, heart rate, electrocardiogram parameters, and depth and rate of breathing in anesthetized beagle dogs did not differ among the IAAS doses or from the vehicle group. These data indicated that IAAS did not induce mutagenicity, clastogenicity, or genotoxicity, and no pharmaco-toxicological effects were observed in the respiratory, cardiovascular, or central nervous systems. Our results increased understanding of safety considerations associated with IAAS, and may indicate that IAAS is a possible drug candidate.

Indexed as

AlstoniascholarisDogsGenotoxicityIndole alkaloids extractMiceSafety pharmacology

Identifiers

PMID32356224
PMCPMC7253540
OpenAlexW3023826204

What OpenQuestion holds

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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.