Evidence map›Paper›PMID 30122142›Full record

ArticlePharmaceutical biology2018

Some pharmacokinetic parameters of salvianolic acid A following single-dose oral administration to rats.

Jialin Sun, Junke Song, Wen Zhang, Fanbo Jing, Wen Xu, Ping Leng, Xianghua Quan, Guanhua Du, Zhongguo Sui

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Salvianolic Acids and Their Pharmacological Promise in Kidney Diseases: A Narrative Review.International journal of nephrology and renovascular disease · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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

9 authors at 3 institutions in 1 country.

Jialin Suna Department of Pharmacy , The Affiliated Hospital of Qingdao University , Qingdao , People's Republic of China.
Junke Songb Beijing Key Laboratory of Drug Target Identification and Drug Screening , Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing , People's Republic of China.
Wen Zhangb Beijing Key Laboratory of Drug Target Identification and Drug Screening , Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing , People's Republic of China.
Fanbo Jinga Department of Pharmacy , The Affiliated Hospital of Qingdao University , Qingdao , People's Republic of China.
Wen Xua Department of Pharmacy , The Affiliated Hospital of Qingdao University , Qingdao , People's Republic of China.
Ping Lenga Department of Pharmacy , The Affiliated Hospital of Qingdao University , Qingdao , People's Republic of China.
Xianghua Quana Department of Pharmacy , The Affiliated Hospital of Qingdao University , Qingdao , People's Republic of China.
Guanhua Dub Beijing Key Laboratory of Drug Target Identification and Drug Screening , Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing , People's Republic of China.
Zhongguo Suia Department of Pharmacy , The Affiliated Hospital of Qingdao University , Qingdao , People's Republic of China.
Affiliated Hospital of Qingdao University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextSalvianolic acid A (Sal A) is a hydrophilic bioactive compound isolated from Salvia miltiorrhiza Bunge (Lamiaceae). It exerts beneficial effects after oral administration on diabetic complications.

objectiveTo systematically study the absorption, distribution and excretion of Sal A after single-dose oral administration. MATERIALS AND

methodsAnimal experiments were conducted in Sprague-Dawley rats. Plasma was sampled at designated times after oral doses of 5, 10 and 20 mg/kg, and an intravenous dose of 50 μg/kg. Tissues were harvested at 10, 60 and 120 min postdosing. Bile, urine and feces were collected at specified intervals before and after dosing. Absorption and distribution characteristics were analyzed by LC-MS, and excretion characteristics were analyzed by UPLC-MS/MS. The Caco-2 cell model was applied to investigate potential mechanisms.

resultsThe C DISCUSSION AND

conclusionsThese results support the future development of Sal A as an oral drug for the treatment of diabetic complications. Future research should be conducted to investigate the reason for its poor bioavailability and improve this situation.

Indexed as

Salvia miltiorrhizaAdministration, OralAnimalsCaco-2 CellsCaffeic AcidsCell Membrane PermeabilityFemaleHumansLactatesMaleProton Pump InhibitorsRatsRats, Sprague-DawleyCaffeic AcidsLactatesProton Pump Inhibitorssalvianolic acid AAbsorptionbioavailabilityeliminationfirst-pass metabolismtransportation

Identifiers

PMID30122142
PMCPMC6130628
OpenAlexW2885767250

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.