Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Claude, Dagenais"'
Autor:
Richard R. Desrosiers, Delara Karkan, Tran Nguyen, Julie Lanthier, Yanick Bertrand, Wilfred A. Jefferies, Michel Demeule, Sam Tsai, Roméo Cecchelli, Claude Dagenais, Richard Béliveau, Julie Poirier, Laurence Fenart, Reinhard Gabathuler, Malcolm L. Kennard, Julie Jodoin
Publikováno v:
Journal of Neurochemistry. 83:924-933
The blood-brain barrier (BBB) performs a neuroprotective function by tightly controlling access to the brain; consequently it also impedes access of proteins as well as pharmacological agents to cerebral tissues. We demonstrate here that recombinant
Publikováno v:
Neuroscience Letters. 301:155-158
P-glycoprotein (P-gp) and organic anion transporting polypeptides (Oatp) are expressed at the blood–brain barrier (BBB). There is little functional evidence for Oatp-mediated transport at the BBB. The peptidic delta opioid-receptor agonist [D-penic
Autor:
Richard Béliveau, Alain Laplante, Anthony Regina, Berthelet F, Albert Moghrabi, Michel Demeule, Julie Jodoin, Claude Dagenais
Publikováno v:
Cancer and Metastasis Reviews. 20:13-25
Malignant brain tumors and brain metastases present a formidable clinical challenge against which no significant advances have been made over the last decade. Multidrug resistance (MDR) is one of the main factors in the failure of chemotherapy agains
Publikováno v:
Pharmaceutical Research. 18:957-963
Purpose. This study assessed the influence of mdr1a P-glycoprotein (P-gp) gene disruption, gender and concentration on initial brain uptake clearance (Clup) of morphine, quinidine and verapamil.
Publikováno v:
Pharmaceutical Research. 18:183-190
Purpose. This study was conducted to assess the influence of P-glycoprotein (P-gp) on brain uptake of multidrug resistance sensitive drugs using an in situbrain perfusion technique in P-gp-deficient (mdr1a[−/−]) and wild-type mice.
Autor:
Linda Foster-Brown, Joseph Milano, Anna Zacco, Claude Dagenais, Barry D. Greenberg, Robert Toms Jacobs, Paul J. Ciaccio, Jenny McKay, Francois Pognan, Reto Gadient
Publikováno v:
Toxicological sciences : an official journal of the Society of Toxicology. 82(1)
It is anticipated that gamma-secretase inhibitors (gamma-Sec-I) that modulate Notch processing will alter differentiation in tissues whose architecture is governed by Notch signaling. To explore this hypothesis, Han Wistar rats were dosed for up to 5
Publikováno v:
Biochemical pharmacology. 67(2)
The efflux transporter P-glycoprotein (P-gp) is an important component of the blood-brain barrier (BBB) that limits accumulation of many compounds in brain. Some opioids have been shown to interact with P-gp in vitro and in vivo. Genetic or chemical
Drug transport to the brain: key roles for the efflux pump P-glycoprotein in the blood-brain barrier
Autor:
Michel Demeule, Anthony Régina, Julie Jodoin, Alain Laplante, Claude Dagenais, France Berthelet, Albert Moghrabi, Richard Béliveau
Publikováno v:
Vascular pharmacology. 38(6)
1. The blood-brain barrier (BBB) contributes to brain homeostastis and fulfills a protective function by controlling the access of solutes and toxic substances to the central nervous system (CNS). The efflux transporter P-glycoprotein (P-gp) is a key
Autor:
Michel, Demeule, Julie, Poirier, Julie, Jodoin, Yanick, Bertrand, Richard R, Desrosiers, Claude, Dagenais, Tran, Nguyen, Julie, Lanthier, Reinhard, Gabathuler, Malcolm, Kennard, Wilfred A, Jefferies, Delara, Karkan, Sam, Tsai, Laurence, Fenart, Roméo, Cecchelli, Richard, Béliveau
Publikováno v:
Journal of neurochemistry. 83(4)
The blood-brain barrier (BBB) performs a neuroprotective function by tightly controlling access to the brain; consequently it also impedes access of proteins as well as pharmacological agents to cerebral tissues. We demonstrate here that recombinant
Publikováno v:
Journal of pharmaceutical sciences. 91(1)
Many opioids are substrates of the efflux transporter P ‐glycoprotein (P‐gp) in the blood–brain barrier (BBB). In situ brain perfusion in wild‐type and mdr 1a (−/−) P‐gp‐deficient mice was utilized to investigate potential P‐gp‐me