Evidence map›Paper›PMID 27367654›Full record

ArticleMolecules (Basel, Switzerland)2016

Relevance of the Pharmacokinetic and Pharmacodynamic Profiles of Puerariae lobatae Radix to Aggregation of Multi-Component Molecules in Aqueous Decoctions.

Bili Su, Yongjun Kan, Jianwei Xie, Juan Hu, Wensheng Pang

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Protein Tyrosine Phosphatase 1B Inhibitors ofMolecules (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Self-assembled aggregations inChinese herbal medicines · 2021
    Article
  5. Review
  6. 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

5 authors.

Bili SuThe Institute of Drug Research, Fujian Academy of Traditional Chinese Medicine, Fuzhou 350003, China. hzf_ketizu@163.com.
Yongjun KanThe Institute of Drug Research, Fujian Academy of Traditional Chinese Medicine, Fuzhou 350003, China. cld_ketizu@163.com.
Jianwei XieThe College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China. 13860662716@163.com.
Juan HuThe Institute of Drug Research, Fujian Academy of Traditional Chinese Medicine, Fuzhou 350003, China. huj@fjtcm.edu.cn.
Wensheng PangThe College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China. pws@fjtcm.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complexity of traditional Chinese medicines (TCMs) is related to their multi-component system. TCM aqueous decoction is a common clinical oral formulation. Between molecules in solution, there exist intermolecular strong interactions to form chemical bonds or weak non-bonding interactions such as hydrogen bonds and Van der Waals forces, which hold molecules together to form "molecular aggregates". Taking the TCM Puerariae lobatae Radix (Gegen) as an example, we explored four Gegen decoctions of different concentration of 0.019, 0.038, 0.075, and 0.30 g/mL, named G-1, G-2, G-3, and G-4. In order of molecular aggregate size (diameter) the four kinds of solution were ranked G-1 < G-2 < G-3 < G-4 by Flow Cell 200S IPAC image analysis. A rabbit vertebrobasilar artery insufficiency (VBI) model was set up and they were given Gegen decoction (GGD) at a clinical dosage of 0.82 g/kg (achieved by adjusting the gastric perfusion volume depending on the concentration). The HPLC fingerprint of rabbit plasma showed that the chemical component absorption into blood in order of peak area values was G-1 < G-2 > G-3 > G-4. Puerarin and daidzin are the major constituents of Gegen, and the pharmacokinetics of G-1 and G-2 puerarin conformed with the two compartment open model, while for G-3 and G-4, they conformed to a one compartment open model. For all four GGDs the pharmacokinetics of daidzin complied with a one compartment open model. FQ-PCR assays of rabbits' vertebrobasilar arterial tissue were performed to determine the pharmacodynamic profiles of the four GGDs. GGD markedly lowered the level of AT₁R mRNA, while the AT₂R mRNA level was increased significantly vs. the VBI model, and G-2 was the most effective. In theory the dosage was equal to the blood drug concentration and should be consistent; however, the formation of molecular aggregates affects drug absorption and metabolism, and therefore influences drugs' effects. Our data provided references for the rational use of Chinese medicines in the clinic, such as the best oral preparation and decoction concentration.

Indexed as

AnimalsChromatography, High Pressure LiquidDisease Models, AnimalDrugs, Chinese HerbalFemaleGene ExpressionIsoflavonesMaleMedicine, Chinese TraditionalPuerariaRabbitsReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2Regional Blood FlowReproducibility of ResultsSensitivity and SpecificitydaidzinDrugs, Chinese HerbalIsoflavonespuerarinReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2Solutionsmolecular aggregationpharmacodynamic profilespharmacokinetic profilesPuerariae lobatae Radix decoction

Identifiers

PMID27367654
PMCPMC6274100

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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.