Evidence map›Paper›PMID 42445281›Full record

ReviewExperimental biology and medicine (Maywood, N.J.)2026

Advances in research on pharmacological mechanisms of anatabine: from nicotinic modulation to multitarget therapeutic potential.

Xiaonan Li, Xiaomin Liu, Huaquan Sheng, Jianfeng Guo, Leihao Zhang, Ting Fei, Yihan Gao

Abstract readReview
In one paragraph

Review in Experimental biology and medicine (Maywood, N.J.), 2026. 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

7 authors.

Xiaonan Li *Basic Research Department, Shanghai New Tobacco Product Research Institute Co., Ltd. (SNTPRI), Shanghai, China.
Xiaomin Liu *Basic Research Department, Shanghai New Tobacco Product Research Institute Co., Ltd. (SNTPRI), Shanghai, China.
Huaquan ShengBasic Research Department, Shanghai New Tobacco Product Research Institute Co., Ltd. (SNTPRI), Shanghai, China.
Jianfeng GuoBasic Research Department, Shanghai New Tobacco Product Research Institute Co., Ltd. (SNTPRI), Shanghai, China.
Leihao ZhangBasic Research Department, Shanghai New Tobacco Product Research Institute Co., Ltd. (SNTPRI), Shanghai, China.
Ting FeiBasic Research Department, Shanghai New Tobacco Product Research Institute Co., Ltd. (SNTPRI), Shanghai, China.
Yihan GaoBasic Research Department, Shanghai New Tobacco Product Research Institute Co., Ltd. (SNTPRI), Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anatabine, a characteristic minor alkaloid derived from tobacco byproducts, exhibits unique structural analogy to nicotine but possesses a superior safety profile and lower addictive liability, rendering it a promising natural multi-target therapeutic candidate. Accumulating preclinical evidence has demonstrated that anatabine exerts neuroprotective, anti-inflammatory, and antioxidant effects mainly through modulating α7/α4β2 nicotinic acetylcholine receptors, suppressing NF-κB/STAT3 inflammatory signaling, and activating the Nrf2-mediated antioxidant pathway. It effectively ameliorates typical pathological alterations, including β-amyloid deposition, tau hyperphosphorylation, and microglial overactivation, thereby improving cognitive and behavioral deficits in neurodegenerative disease models. Additionally, anatabine displays broad pharmacological potentials in chronic inflammation, autoimmune thyroiditis, asthma, and hypertension. Differing from previous reviews that merely focused on single receptor regulation, the present work systematically summarizes the multi-target pharmacological characteristics of anatabine, comprehensively collates its preclinical efficacy across multiple disease categories, and highlights its advantages over nicotine in safety and addiction risk. Furthermore, we analyze the current limitations, druggability optimization challenges, and clinical translation prospects, and propose sustainable strategies for high-value utilization of tobacco byproducts. This review provides an updated and systematic theoretical basis for further mechanism exploration and therapeutic development of anatabine.

Indexed as

AlkaloidsPyridinesReceptors, NicotinicAnimalsAnti-Inflammatory AgentsAntioxidantsHumansNeuroprotective AgentsAlkaloidsanatabineAnti-Inflammatory AgentsAntioxidantsNeuroprotective AgentsPyridinesReceptors, NicotinicalkaloidsAlzheimer’s diseaseanatabineanti-inflammatoryneurological disordersNF-κBpharmacological mechanisms

Identifiers

PMID42445281
PMCPMC13357314

What OpenQuestion holds

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LicenceCC BY
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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.