Inhibitors of ABC drug transporters at the blood-brain barrier
The present invention relates to inhibitors of drug transporters of the ABC protein superfamily, particularly transporters present at the blood brain barrier. ABC transporter inhibitors identified according to the invention increase brain concentrations of CNS-active agents. Such inhibitors increase the influx into the brain and/or reduce the efflux from the brain of such CNS-active agents.
1. A composition comprising
(a) a non-opioid CNS-active agent, wherein the said non-opioid CNS agent is selected from the group consisting of diazepam, lithium, triazolam, and zolpidem, and
(b) an ABC drug transporter protein-inhibiting amount of an opioid inhibitor of an ABC drug transporter, wherein the amount is in the range of from 3 ng/kg to 3000 ng/kg.
2. The composition of claim 1 , wherein the ABC drug transporter is a PGP drug transporter.
3. The composition of claim 2 , wherein the PGP drug transporter is a PGP1a drug transporter.
4. The composition of claim 1 , wherein the opioid inhibitor is an opioid receptor antagonist.
5. The composition of claim 4 , wherein the opioid receptor antagonist is a compound of the formula:
wherein R 1 is CH 2 or O;
wherein R 2 is a cycloalkyl, unsubstituted aromatic, alkyl or alkenyl; and
wherein R 3 is O, CH 2 or NH.
6. The composition of claim 4 , wherein the opioid receptor antagonist is selected from the group consisting of naltrexone, naloxone, and nalmefene.
7. The composition of claim 1 , wherein the inhibitor is a compound of the formula:
wherein R 1 is CH 2 or O;
wherein R 2 is a cycloalkyl, unsubstituted aromatic, alkyl or alkenyl; and
wherein R 3 is O, CH 2 or NH.
8. A composition comprising:
(a) a non-opioid CNS-active agent wherein the said non-opioid CNS agent is selected from the group consisting of diazepam, lithium, triazolam, and zolpidem, and
(b) an ABC drug transporter protein-inhibiting amount of an opioid receptor antagonist that is an inhibitor of an ABC drug transporter, wherein the amount is in the range of from 3 ng/kg to 3000 ng/kg;
wherein the composition is for the treatment of chronic pain, for controlling pain without dependence, tolerance, or withdrawal.
9. The composition of claim 8 , wherein the opioid receptor antagonist is selected from the group consisting of naltrexone, naloxone, and nalmefene.
10. The composition of claim 8 , wherein the opioid receptor antagonist is a compound of the formula:
wherein R 1 is CH 2 or O;
wherein R 2 is a cycloalkyl, unsubstituted aromatic, alkyl or alkenyl; and
wherein R 3 is O, CH 2 or NH.