Role of metabolism by intestinal microbiota in pharmacokinetics of oral baicalin

Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension, cardiovascular diseases, and viral hepatitis. In this study, the effects of intestinal microbiota on the pharmacokinetics of baicalin were in...

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Published inArchives of pharmacal research Vol. 37; no. 3; pp. 371 - 378
Main Authors Kang, Mi Jeong, Ko, Gyu Sub, Oh, Do Gyeong, Kim, Jin Sung, Noh, Keumhan, Kang, Wonku, Yoon, Won Ki, Kim, Hyoung Chin, Jeong, Hye Gwang, Jeong, Tae Cheon
Format Journal Article
LanguageEnglish
Published Heidelberg Pharmaceutical Society of Korea 01.03.2014
대한약학회
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Online AccessGet full text
ISSN0253-6269
1976-3786
1976-3786
DOI10.1007/s12272-013-0179-2

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Abstract Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension, cardiovascular diseases, and viral hepatitis. In this study, the effects of intestinal microbiota on the pharmacokinetics of baicalin were investigated in normal and antibiotic-pretreated rats following p.o. administration of 100 mg/kg baicalin by using liquid chromatography/ion trap mass spectrometry. When rats were pretreated orally with cefadroxil, oxytetracycline and erythromycin for 3 days to control the number of intestinal bacteria, the pharmacokinetic parameters of oral baicalin were significantly affected by antibiotics: C max , T 1/2(β) , K el and AUC values were significantly changed compared to those in normal rats. These results indicate that intestinal microbiota might play a key role in the oral pharmacokinetics of baicalin.
AbstractList Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension, cardiovascular diseases, and viral hepatitis. In this study, the effects of intestinal microbiota on the pharmacokinetics of baicalin were investigated in normal and antibiotic-pretreated rats following p.o. administration of 100 mg/kg baicalin by using liquid chromatography/ion trap mass spectrometry. When rats were pretreated orally with cefadroxil, oxytetracycline and erythromycin for 3 days to control the number of intestinal bacteria, the pharmacokinetic parameters of oral baicalin were significantly affected by antibiotics: Cmax, T1/2(β), Kel and AUC values were significantly changed compared to those in normal rats. These results indicate that intestinal microbiota might play a key role in the oral pharmacokinetics of baicalin.
Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension, cardiovascular diseases, and viral hepatitis. In this study, the effects of intestinal microbiota on the pharmacokinetics of baicalin were investigated in normal and antibiotic-pretreated rats following p.o. administration of 100 mg/kg baicalin by using liquid chromatography/ion trap mass spectrometry. When rats were pretreated orally with cefadroxil, oxytetracycline and erythromycin for 3 days to control the number of intestinal bacteria, the pharmacokinetic parameters of oral baicalin were significantly affected by antibiotics: Cmax, T1/2(β), Kel and AUC values were significantly changed compared to those in normal rats. These results indicate that intestinal microbiota might play a key role in the oral pharmacokinetics of baicalin.Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension, cardiovascular diseases, and viral hepatitis. In this study, the effects of intestinal microbiota on the pharmacokinetics of baicalin were investigated in normal and antibiotic-pretreated rats following p.o. administration of 100 mg/kg baicalin by using liquid chromatography/ion trap mass spectrometry. When rats were pretreated orally with cefadroxil, oxytetracycline and erythromycin for 3 days to control the number of intestinal bacteria, the pharmacokinetic parameters of oral baicalin were significantly affected by antibiotics: Cmax, T1/2(β), Kel and AUC values were significantly changed compared to those in normal rats. These results indicate that intestinal microbiota might play a key role in the oral pharmacokinetics of baicalin.
Baicalin (baicalein-7-glucuronide) is a flavonoidpurified from Scutellaria baicalensis Georgi that hastraditionally been used for treatment of hypertension, cardiovasculardiseases, and viral hepatitis. In this study, theeffects of intestinal microbiota on the pharmacokinetics ofbaicalin were investigated in normal and antibiotic-pretreatedrats following p.o. administration of 100 mg/kgbaicalin by using liquid chromatography/ion trap massspectrometry. When rats were pretreated orally with cefadroxil,oxytetracycline and erythromycin for 3 days tocontrol the number of intestinal bacteria, the pharmacokineticparameters of oral baicalin were significantly affectedby antibiotics: Cmax, T1/2(b), Kel and AUC values weresignificantly changed compared to those in normal rats. These results indicate that intestinal microbiota might playa key role in the oral pharmacokinetics of baicalin. KCI Citation Count: 51
Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension, cardiovascular diseases, and viral hepatitis. In this study, the effects of intestinal microbiota on the pharmacokinetics of baicalin were investigated in normal and antibiotic-pretreated rats following p.o. administration of 100 mg/kg baicalin by using liquid chromatography/ion trap mass spectrometry. When rats were pretreated orally with cefadroxil, oxytetracycline and erythromycin for 3 days to control the number of intestinal bacteria, the pharmacokinetic parameters of oral baicalin were significantly affected by antibiotics: Cₘₐₓ, T₁/₂₍ᵦ₎, Kₑₗand AUC values were significantly changed compared to those in normal rats. These results indicate that intestinal microbiota might play a key role in the oral pharmacokinetics of baicalin.
Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension, cardiovascular diseases, and viral hepatitis. In this study, the effects of intestinal microbiota on the pharmacokinetics of baicalin were investigated in normal and antibiotic-pretreated rats following p.o. administration of 100 mg/kg baicalin by using liquid chromatography/ion trap mass spectrometry. When rats were pretreated orally with cefadroxil, oxytetracycline and erythromycin for 3 days to control the number of intestinal bacteria, the pharmacokinetic parameters of oral baicalin were significantly affected by antibiotics: C max , T 1/2(β) , K el and AUC values were significantly changed compared to those in normal rats. These results indicate that intestinal microbiota might play a key role in the oral pharmacokinetics of baicalin.
Author Kang, Mi Jeong
Noh, Keumhan
Oh, Do Gyeong
Kim, Hyoung Chin
Jeong, Tae Cheon
Yoon, Won Ki
Jeong, Hye Gwang
Ko, Gyu Sub
Kang, Wonku
Kim, Jin Sung
Author_xml – sequence: 1
  givenname: Mi Jeong
  surname: Kang
  fullname: Kang, Mi Jeong
  organization: College of Pharmacy, Yeungnam University
– sequence: 2
  givenname: Gyu Sub
  surname: Ko
  fullname: Ko, Gyu Sub
  organization: College of Pharmacy, Yeungnam University
– sequence: 3
  givenname: Do Gyeong
  surname: Oh
  fullname: Oh, Do Gyeong
  organization: College of Pharmacy, Yeungnam University
– sequence: 4
  givenname: Jin Sung
  surname: Kim
  fullname: Kim, Jin Sung
  organization: College of Pharmacy, Yeungnam University
– sequence: 5
  givenname: Keumhan
  surname: Noh
  fullname: Noh, Keumhan
  organization: College of Pharmacy, Yeungnam University
– sequence: 6
  givenname: Wonku
  surname: Kang
  fullname: Kang, Wonku
  organization: College of Pharmacy, Yeungnam University
– sequence: 7
  givenname: Won Ki
  surname: Yoon
  fullname: Yoon, Won Ki
  organization: Korea Research Institute of Bioscience and Biotechnology
– sequence: 8
  givenname: Hyoung Chin
  surname: Kim
  fullname: Kim, Hyoung Chin
  organization: Korea Research Institute of Bioscience and Biotechnology
– sequence: 9
  givenname: Hye Gwang
  surname: Jeong
  fullname: Jeong, Hye Gwang
  organization: College of Pharmacy, Chungnam National University
– sequence: 10
  givenname: Tae Cheon
  surname: Jeong
  fullname: Jeong, Tae Cheon
  email: taecheon@yumail.ac.kr, taecheon@ynu.ac.kr
  organization: College of Pharmacy, Yeungnam University
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Metabolism
Baicalin
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Snippet Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension,...
Baicalin (baicalein-7-glucuronide) is a flavonoid purified from Scutellaria baicalensis Georgi that has traditionally been used for treatment of hypertension,...
Baicalin (baicalein-7-glucuronide) is a flavonoidpurified from Scutellaria baicalensis Georgi that hastraditionally been used for treatment of hypertension,...
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SubjectTerms Administration, Oral
Animals
baicalin
cefadroxil
erythromycin
Flavonoids - administration & dosage
Flavonoids - pharmacokinetics
Intestinal Absorption - drug effects
Intestinal Absorption - physiology
intestinal microorganisms
Intestinal Mucosa - drug effects
Intestinal Mucosa - metabolism
liquid chromatography
Male
mass spectrometry
Medicine
Microbiota - drug effects
Microbiota - physiology
oxytetracycline
pharmacokinetics
Pharmacology/Toxicology
Pharmacy
Rats
Rats, Sprague-Dawley
Research Article
Scutellaria
Scutellaria baicalensis
약학
Title Role of metabolism by intestinal microbiota in pharmacokinetics of oral baicalin
URI https://link.springer.com/article/10.1007/s12272-013-0179-2
https://www.ncbi.nlm.nih.gov/pubmed/23771520
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