Techniques of treating neurodegenerative disorders by brain infusion

• US 5,735,814 A
• Filed: 04/30/1996
• Issued: 04/07/1998
• Est. Priority Date: 04/30/1996
• Status: Expired due to Term

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Rise, Mark T., Elsberry, Dennis D.
• Primary Examiner(s): Buiz, Michael
• Assistant Examiner(s): TRUONG, KEVIN THAO
• Application Number:
  US08/640,358
• Time in Patent Office: 707 Days
• Field of Search: 604/43, 604/49, 604/50, 604/51, 604/93, 604/891.1
• US Class Current: 604/43
• CPC Class Codes: A61M 2210/0693 Brain, cerebrum
• CPC Class Codes: A61M 5/14276 specially adapted for implantation
• CPC Class Codes: A61M 5/1723 using feedback of body parameters, e.g. blood-sugar, pressure measurement of body parameters A61B5/00

Abstract

Techniques for infusing drugs into the brain to treat neurodegenerative disorders by an implantable pump and catheter. The drugs are capable of altering the level of excitation of neruons in the brain. A sensor is used to detect an attribute of the nervous system which reflects the hyperexcitation of the nerve cells projecting onto the degenerating nerve cells. A microprocessor algorithm analyzes the output from the sensor in order to regulate the amount of drug delivered to the brain.

Claims

1. A method of treating a neurodegenerative disorder by means of an implantable pump and a catheter having a discharge portion and having a proximal end coupled to said pump, said method comprising the steps of:

surgically implanting said catheter so that said discharge portion lies adjacent a predetermined infusion site in a brain; and

operating said pump to discharge a predetermined dosage of at least one drug capable of altering the level of excitation of neurons of said brain through said discharge portion of said catheter into said infusion site, whereby neurodegeneration is prevented and said neurodegenerative disorder is therapeutically treated.

2. A method, as claimed in claim 1, wherein said step of implanting said catheter is performed as soon as practical after said neurodegenerative disorder is diagnosed.

3. A method, as claimed in claim 1, and further comprising the steps of:

implanting said pump outside said brain; and

periodically refreshing the supply of said at least one drug to said pump outside said brain.

4. A method, as claimed in claim 1, wherein said neurodegenerative disorder is Parkinson'"'"'s disease;

wherein said predetermined infusion site is selected from the group consisting of ventrolateral thalamus (Thal), internal segment of globus pallidus (GPi), substantia nigra pars reticulata (SNr), subthalamic nucleus (STN), external segment of globus pallidus (GPe), neostriatum, cerebral ventricle, subdural space, intrathecal space; and

wherein said drug is selected to reduce hyperexcitation.

5. A method, as claimed in claim 4, wherein said at least one drug increases excitement of the thalamus.

6. A method, as claimed in claim 4, wherein said at least one drug increases inhibition of at least one of said internal segment of globus pallidus (GPi) and said substantia nigra pars reticulata (SNr) that inhibit thalamic output.

7. A method, as claimed in claim 4, wherein said at least one drug decreases excitement of the subthalamus.

8. A method, as claimed in claim 4, wherein said at least one drug decreases inhibition of said external segment of globus pallidus (Gpe).

9. A method, as claimed in claim 4, wherein said at least one drug is selected from the group consisting of a glutamate antagonist, a glutamate agonist, a a γ

aminobutyric acid (GABA) antagonist, a γ

-aminobutyric acid (GABA) agonist, a dopamine (DA) antagonist, a dopamine (DA) agonist and an anesthetic.

10. A method, as claimed in claim 4, wherein said at least one drug decreases inhibition of the thalamus.

11. A method, as claimed in claim 4, wherein said at least one drug decreases excitation of at least one of said internal segment of globus pallidus (GPi) and said substantia nigra pars reticulata (SNr) that inhibit thalamic output.

12. A method, as claimed in claim 4, wherein said at least one drug increases inhibition of the subthalamus.

13. A method, as claimed in claim 4, wherein said at least one drug increases excitation of said external segment of globus pallidus (Gpe).

14. A method, as claimed in claim 1, wherein said neurodegenerative disorder comprises amyotrophic lateral sclerosis,

wherein said predetermined infusion site is selected from the group consisting of ventrolateral thalamus (Thal), internal segment of globus pallidus (GPi), substantia nigra pars reticulata (SNr), subthalamic nucleus (STN), external segment of globus pallidus (GPe), neostriatum, cerebral ventricle, subdural space, intrathecal space;

and

wherein said drugs is selected to reduce hyperexcitation.

15. A method, as claimed in claim 14, wherein said at least one drug decreases excitement of the thalamus.

16. A method, as claimed in claim 14, wherein said at least one drug decreases inhibition at least one of said internal segment of globus pallidus (GPi) and said substantia nigra pars reticulata (Snr).

17. A method, as claimed in claim 14, wherein said at least one drug decrease inhibition of said subthalamic nucleus (STN).

18. A method, as claimed in claim 14, wherein said at least one drug decreases excitation of at least one of said external segment of globus pallidus (GPe) and motorcortex and anterior horn of the spinal cord.

19. A method, as claimed in claim 14, wherein at least one drug decreases excitation of dopaminergic neurons in the neostriatum.

20. A method, as claimed in claim 4, wherein said at least one drug is selected from the group consisting of a glutamate antagonist, a glutamate agonist, a y-aminobutyric acid (GABA) antagonist, a y-aminobutyric acid (GABA) agonist, a dopamine (DA) antagonist, a dopamine (DA) agonist and an anesthetic.

21. A method, as claimed in claim 14, wherein said at least one drug increases inhibition of the thalamus.

22. A method, as claimed in claim 14, wherein said at least one drug increases excitation of at least one of said internal segment of globus pallidus (GPi) and said substantia nigra pars reticulata (Snr).

23. A method, as claimed in claim 14, wherein said at least one drug increases excitation of said subthalamic nucleus (STN).

24. A method, as claimed in claim 14, wherein said at least one drug increases inhibition of at least one of said external segment of globus pallidus (GPe), motorcortex and anterior horn of the spinal cord.

25. A method, as claimed in claim 1, wherein said neurodegenerative disorder comprises Huntington'"'"'s disease;

wherein said predetermined infusion site is selected from the group consisting of ventrolateral thalamus (Thai), internal segment of globus pallidus (GPi), substantia nigra pars reticulata (SNr), subthalamic nucleus (STN), external segment of globus pallidus (GPe), neostriatum, cerebral ventricle, subdural space, intrathecal space; and

wherein said drug is selected to reduce hyperexcitation.