Studies on pharmacokinetic mechanism of phenytoin resistance in refractory epilepsy. Issue 9 (8th May 2013)
- Record Type:
- Journal Article
- Title:
- Studies on pharmacokinetic mechanism of phenytoin resistance in refractory epilepsy. Issue 9 (8th May 2013)
- Main Title:
- Studies on pharmacokinetic mechanism of phenytoin resistance in refractory epilepsy
- Authors:
- Lai, Ming‐Liang
Tien, Yu‐En
Huang, Ying‐Syuan
Huang, Jin‐Ding
Nakashima, Emi
Brouwer, Kim
Hammarlund‐Udenaes, Margareta
Terasaki, Tetsuya - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>P‐glycoprotein (P‐gp) is a drug efflux pump in many organs, including the intestine and liver. Two single nucleotide polymorphisms (SNPs) of P‐gp gene, 2677G&gt;T and 3435C&gt;T, were reported to influence function and expression of P‐gp and have the controversial effects on drug disposition. Phenytoin is one substrate of P‐gp. Persistent low phenytoin levels in plasma and P‐gp overexpression in brain in several refractory epilepsy patients were reported. P‐gp polymorphisms may also affect phenytoin efficacy by altering its bioavailability (<italic>F</italic>). Because two P‐gp SNPs, 2677G&gt;T and 3435C&gt;T, may affect P‐gp expression in tissue, we examined phenytoin disposition in patients of different P‐gp haplotypes, G/G2677C/C3435 and T/T2677T/T3435. We found that the mean absolute <italic>F</italic> of phenytoin in T/T2677T/T3435 subjects (91%) is slightly higher than in G/G2677C/C3435 subjects (82%). There was no difference in the maximum concentration (<italic>C</italic><sub>max</sub>) and the area under the serum concentration–time curve of phenytoin administered orally between two genotypic groups. However, the time of maximum concentration was higher in T/T2677T/T3435 subjects (10 h) than in G/G2677C/C3435 subjects (6 h). The study ruled out the possibility that genetic polymorphisms of P‐gp may affect phenytoin efficacy through the decreased absorption or the increased elimination. P‐gp<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>P‐glycoprotein (P‐gp) is a drug efflux pump in many organs, including the intestine and liver. Two single nucleotide polymorphisms (SNPs) of P‐gp gene, 2677G&gt;T and 3435C&gt;T, were reported to influence function and expression of P‐gp and have the controversial effects on drug disposition. Phenytoin is one substrate of P‐gp. Persistent low phenytoin levels in plasma and P‐gp overexpression in brain in several refractory epilepsy patients were reported. P‐gp polymorphisms may also affect phenytoin efficacy by altering its bioavailability (<italic>F</italic>). Because two P‐gp SNPs, 2677G&gt;T and 3435C&gt;T, may affect P‐gp expression in tissue, we examined phenytoin disposition in patients of different P‐gp haplotypes, G/G2677C/C3435 and T/T2677T/T3435. We found that the mean absolute <italic>F</italic> of phenytoin in T/T2677T/T3435 subjects (91%) is slightly higher than in G/G2677C/C3435 subjects (82%). There was no difference in the maximum concentration (<italic>C</italic><sub>max</sub>) and the area under the serum concentration–time curve of phenytoin administered orally between two genotypic groups. However, the time of maximum concentration was higher in T/T2677T/T3435 subjects (10 h) than in G/G2677C/C3435 subjects (6 h). The study ruled out the possibility that genetic polymorphisms of P‐gp may affect phenytoin efficacy through the decreased absorption or the increased elimination. P‐gp SNPs could affect phenytoin efficacy in refractory epilepsy patients probably because of central nervous system. © 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:3189–3195, 2013</p> </abstract> … (more)
- Is Part Of:
- Journal of pharmaceutical sciences. Volume 102:Issue 9(2013:Sep.)
- Journal:
- Journal of pharmaceutical sciences
- Issue:
- Volume 102:Issue 9(2013:Sep.)
- Issue Display:
- Volume 102, Issue 9 (2013)
- Year:
- 2013
- Volume:
- 102
- Issue:
- 9
- Issue Sort Value:
- 2013-0102-0009-0000
- Page Start:
- 3189
- Page End:
- 3195
- Publication Date:
- 2013-05-08
- Subjects:
- Pharmacy -- Periodicals
615.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-6017 ↗
http://www.jpharmsci.org/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jps.23593 ↗
- Languages:
- English
- ISSNs:
- 0022-3549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5031.900000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3000.xml