Method of treating and preventing brain impairment using Na
The disclosure relates to a method of treating and/or preventing brain impairment in a subject that has or is susceptible to ammonia neurotoxicity (increased plasma ammonia), by administering a Na-; —K+-2CI- cotransporter isoform 1 (“NKCC1”) inhibitor to the selected subject under conditions effective to treat and/or prevent brain impairment. The disclosure further relates to methods of maintaining the fundamental function of astrocytic potassium buffering and inhibiting accumulation of potassium star rounding astrocytes, both of which involve contacting astrocytes with a NKCC 1 inhibitor.
1. A method of treating epileptic seizures in a subject comprising:
selecting a subject susceptible to epileptic seizures and having ammonia neurotoxicity in astrocytes, and
administering a Na + -K + -2Cl − cotransporter isoform 1 (“NKCC1”) inhibitor to the selected subject under conditions effective to treat epileptic seizures.
2. The method of claim 1 , wherein the NKCC1 inhibitor is selected from the group consisting of bumetanide, furosemide, piretanide, azosemide, ethacrynic acid, torsemide, muzolimine, tripamide, and etozolin.
3. The method of claim 1 further comprising:
repeating said administering.
4. The method of claim 1 , wherein said administering is carried out orally, by inhalation, by intranasal instillation, topically, transdermally, parenterally, subcutaneously, intravenous injection, intra-arterial injection, intramuscular injection, intraplurally, intraperitoneally, or by application by mucous membrane.
5. A method of inhibiting accumulation of potassium surrounding astrocytes comprising:
selecting a subject exhibiting accumulation of potassium surrounding astrocytes, and
administering to the selected subject a Na + -K + -2Cl − cotransporter isoform 1 (“NKCC1”) inhibitor under conditions effective to inhibit accumulation of potassium surrounding the astrocytes.
6. The method of claim 5 , wherein the NKCC1 inhibitor is selected from the group consisting of bumetanide, furosemide, piretanide, azosemide, ethacrynic acid, torsemide, muzolimine, tripamide, and etozolin.
7. The method of claim 1 further comprising administering a second agent.