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Developmental Aspects of Drug Transport Across the Blood-Brain Barrier

Bengtsson, Jörgen, 1976- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Margareta Hammarlund-Udenaes
Hammarlund-Udenaes, Margareta, Prof (preses)
Uppsala universitet,Avdelningen för farmakokinetik och läkemedelsterapi
Engwall, Ann-Cathrin (preses)
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Björkman, Sven, Prof (preses)
Uppsala universitet,Avdelningen för farmakokinetik och läkemedelsterapi
de Lange, Elizabeth C.M. Dr (opponent)
Leiden/Amsterdam Center for Drug Research, Division of Pharmacology, The Netherlands
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 (creator_code:org_t)
ISBN 9789155476274
Uppsala : Acta Universitatis Upsaliensis, 2009
Engelska 60 s.
Serie: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Pharmacy, 1651-6192 ; 110
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
Stäng  
  • The developmental aspect of drug transport across the blood-brain barrier (BBB) was investigated. Microdialysis was used to study unbound morphine BBB transport at different ages in sheep. An in vitro study was performed to find differentially expressed genes in brain capillary-rich fractions of the brain in rats of different ages. Microdialysis and brain-to-plasma ratios were used to study the contribution of breast cancer resistance protein (Bcrp) to the transport of nitrofurantoin (NTF) across the BBB of rats during development as well as in adult rats and mice. A method of analysing morphine and its metabolites in plasma and microdialysis samples was developed and validated. The in vivo recovery of deuterated morphine, used as a calibrator in microdialysis experiments, was not affected by the presence of morphine in the tissue. A net influx of morphine was observed in premature lambs and adult sheep, in contrast to the efflux seen in other species. This influx decreased with age, indicating that the morphine transport across the BBB changes with age. In contrast, the transport of the morphine metabolite morphine-3-glucuronide (M3G) did not change with age. Microarray data indicated that several active transporters are differentially expressed with age. Moreover, the mRNA expression levels of Abcg2 (Bcrp) and Slc22a8 (organic anion transporter 3) changed with age when quantified using real-time polymerase chain reaction. In contrast, the expression of Abcb1 (P-glycoprotein) and occludin (a tight junction protein) did not change with age. In rats, the brain distribution of NTF decreased with age due to increased protein binding in plasma. The concentration ratio of unbound NTF across the BBB was low in the adult rat, due to intra-brain metabolism and/or efflux by other transporters. Bcrp did not appear to have a significant contribution in the developing rat or in knock-out mice compared to wild-type controls with regard to NTF BBB transport. In conclusion, in vitro studies showed that the expression levels of some genes changed with age, presumably affecting subsequent drug distribution to the brain. Further, in vivo studies showed that distribution across the BBB changed with age for morphine but not for M3G or NTF.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Nyckelord

Blood-brain barrier
development
active transport
tight junction proteins
microdialysis
recovery
morphine
nitrofurantoin
Bcrp
microarray
real-time PCR
in vitro
in vivo
LC-MS/MS
Biopharmacy
Biofarmaci
Pharmacokinetics and Drug Therapy
Farmakokinetik och läkemedelsterapi

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