IP Library Granted Patent US 7,689,277
Granted Patent B2
US 7,689,277 · App. 11/338,388 · Granted Mar 30, 2010

Neural stimulation for treatment of metabolic syndrome and type 2 diabetes

Assignee: Leptos Biomedical, Inc.
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Quick Facts
Patent No.
US 7,689,277
App. No.
11/338,388
Granted
Mar 30, 2010
Kind
B2
Abstract

Systems and methods are described for treating metabolic syndrome and/or Type 2 diabetes, and/or one or more of their attendant conditions, by neural stimulation. In one embodiment, an implantable pulse generator is electrically coupled to a peripheral nerve, such as the splanchnic nerve. Neural stimulation configured to either block transmission or stimulate transmission of the peripheral nerve may be used to treat metabolic syndrome and Type 2 diabetes.

Claims (25)

1. A method, of treating at least dyslipidemia comprising:

selecting a patient suffering from dyslipidemia;

electrically modulating a splanchnic nerve of the patient in a stimulation pattern that ameliorates or eliminates dyslipidemia;

wherein said stimulation pattern comprises a stimulation intensity, and said stimulation intensity is between 0.005 and 5.0 mA-msec;

wherein said stimulation pattern comprises an on time and an off time; and wherein said off time is no less than said on time;

wherein said stimulation pattern comprises a frequency, a pulse width, and a current; and

wherein said frequency is between 0.1 Hz and 50 Hz; said pulse width is between 100 microseconds and 1 millisecond; and said current is between 0.1 mA and 10 mA.

2. The method of claim 1 , further comprising: providing a first electrical signal to said nerve at a first stimulation intensity during a first portion of a first stimulation time period; applying a second electrical signal to said nerve at a second stimulation intensity during a second portion of a first stimulation time period; ceasing or substantially reducing said applying of said second signal during a first no-stimulation time period; thereafter, applying a third electrical signal to said nerve at a third stimulation intensity during a first portion of a second stimulation time period; applying a fourth electrical signal to the nerve at a fourth stimulation intensity during a second portion of a second stimulation time period; and ceasing or substantially reducing said applying of said fourth signal during a second no-stimulation period.

3. The method of claim 1 , further comprising:

applying a first plurality of temporally sequential electrical signals during a first plurality of respective stimulation periods, each of said first plurality of signals having a stimulation intensity that is greater than the stimulation intensity of the preceding signal;

thereafter, ceasing or substantially reducing electrical stimulation to said nerve during a first no-stimulation period;

thereafter, applying a second plurality of temporally sequential electrical signals during a second plurality of respective stimulation periods, each of said second plurality of signals having a stimulation intensity that is greater than the stimulation intensity of the preceding signal; and

thereafter, ceasing or substantially reducing electrical stimulation to said nerve during a second no-stimulation period.

4. The method of claim 1 , further comprising;

electrically stimulating said nerve for a first time and at a first stimulation intensity;

thereafter, electrically stimulating said nerve for a second time and at a second stimulation intensity, said second stimulation intensity being greater than said first stimulation intensity; and

thereafter, providing a period during which electrical stimulation at said nerve is absent or substantially less than the second stimulation intensity.

5. The method of claim 1 , wherein said patient has dyslipidemia and hypertension.

6. The method of claim 1 , wherein said patient has dyslipidemia and hyperglycemia.

7. The method of claim 1 , wherein said patient has dyslipidemia and hyperinsulinemia.

8. The method of claim 1 , wherein said patient has dyslipidemia and insulin resistance.

9. The method of claim 1 , wherein said dyslipidemia comprises decreased HDL, and said stimulation pattern increases HDL.

10. The method of claim 1 , wherein said dyslipidemia comprises elevated triglycerides, and said stimulation pattern decreases triglycerides.

11. The method of claim 1 , wherein said dyslipidemia comprises elevated LDL, and said stimulation pattern decreases LDL.

12. The method of claim 1 , wherein said stimulation pattern includes a stimulation intensity ramping portion extending over a plurality of days and a substantial reduction in stimulation intensity portion occurring after the stimulation intensity ramping portion.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2010
From: LEPTOS BIOMEDICAL INC.
To: ADVANCED NEUROMODULATION SYSTEMS, INC. D/B/A ST. JUDE MEDICAL NEUROMODULATION DIVISION
Reel/Frame 024369/0898 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2006
From: DOBAK, JOHN D. III
To: LEPTOS BIOMEDICAL, INC.
Reel/Frame 017824/0896 →
Continuity (17)
Continuation In Part 1092073400 · Aug 18, 2004
Continuation In Part 1078572600 · Feb 24, 2004
Continuation In Part 1027243000 · Oct 16, 2002
Continuation In Part 1024361200 · Sep 13, 2002
Provisional Application 6049643700 · Aug 20, 2003
Provisional Application 6036675000 · Mar 22, 2002
Provisional Application 6037031100 · Apr 5, 2002
Provisional Application 6037960500 · May 10, 2002
Provisional Application 6038421900 · May 30, 2002
Provisional Application 6038669900 · Jun 10, 2002
Provisional Application 6045053400 · Feb 25, 2003
Provisional Application 6045236100 · Mar 5, 2003
Provisional Application 6046689000 · Apr 30, 2003
Provisional Application 6046680500 · Apr 30, 2003
Provisional Application 6047993300 · Jun 19, 2003
Provisional Application 6049643700 · Aug 20, 2003
Related Publication 20060190053A1 · Aug 24, 2006