ReviewNaunyn-Schmiedeberg's archives of pharmacology2026
Rhizoma Paridis saponins in respiratory diseases: a narrative review of multi-target mechanisms and therapeutic potential.
Review in Naunyn-Schmiedeberg's archives of pharmacology, 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
Rhizoma Paridis saponins (RPS) are bioactive constituents of Rhizoma Paridis with reported anti-inflammatory and antitumor activities. However, their roles in respiratory diseases remain incompletely understood. This study is a narrative review rather than a systematic review. A narrative literature review was conducted using PubMed and CNKI databases to retrieve studies published between 2014 and 2025. Keywords included "Rhizoma Paridis," "polyphyllin," and "respiratory diseases." Studies were selected based on relevance to respiratory disease mechanisms and pharmacological evidence. RPS and its derivatives exhibit multi-target regulatory activities across respiratory disease models, including chronic obstructive pulmonary disease (COPD), pulmonary hypertension (PH), pulmonary fibrosis (PF), and lung cancer. These effects are primarily mediated through modulation of inflammation, oxidative stress, apoptosis, and key signaling pathways such as NF-κB, PI3K/AKT, MAPK, and Nrf2. Current evidence is exclusively derived from preclinical studies, including in vitro and in vivo experimental models, with no clinical data available in humans. Although RPS demonstrates promising multi-target pharmacological effects in respiratory disease models, these findings should be interpreted with caution. Further pharmacokinetic, toxicological, and clinical studies are required to evaluate its translational potential.
Indexed as
Identifiers
42448932What 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.