Methods of treating and/or preventing neurodevelopmental disorders (autism) using aminosterols
This invention relates to methods of stimulating the activity of the human and animal enteric nervous system. The method comprises orally administering an aminoserol, such as squalamine, a naturally occurring aminosterol isolated from Squalus acanthias , or derivatives thereof, to a subject in need.
1. A method of treating a neurodegenerative disease which is autism in a subject, comprising orally administering to the subject a composition comprising a pharmaceutically acceptable grade of at least one aminosterol, or a pharmaceutically acceptable salt or derivative thereof, in an amount sufficient to produce a beneficial effect.
2. The method of claim 1 , wherein administration of the aminosterol induces production of neuro-protective hormones which provide a therapeutic benefit.
3. The method of claim 1 , wherein the beneficial effect results from the effects of the aminosterol on enteric neurons.
4. The method of claim 1 , wherein the beneficial effect is the result of the aminosterol triggering the stimulation of electrical signals flowing through the afferent arm of the vagus.
5. The method of claim 1 , wherein the compound is an aminosterol that can inhibit the formation of actin stress fibers in endothelial cells stimulated by a ligand known to induce stress fiber formation, having the chemical structure of Formula I:
wherein:
W is 24S—OSO 3 H or 24R—OSO 3 H;
X is 3β-H 2 N—(CH 2 ) 4 —NH—(CH 2 ) 3 —NH— or 3α-H 2 N—(CH 2 ) 4 —NH—(CH 2 ) 3 —NH—;
Y is 20R—CH 3 ; and
Z is 7α or 7β —OH.
6. The method of claim 1 , wherein the aminosterol is represented by the family of related compounds (compounds 1-8) isolated from Squalus acanthias :
7. The method of claim 1 , wherein the aminosterol is Aminosterol 1436 (Compound 7).
8. The method of claim 1 , wherein the aminosterol is a squalamine isomer.
9. The method of claim 1 , wherein the aminosterol comprises a sterol nucleus and a polyamine, attached at any position on the sterol, such that the molecule exhibits a net charge of at least +1, the charge being contributed by the polyamine.
10. The method of claim 1 , wherein the aminosterol comprises a bile acid nucleus and a polyamine, attached at any position on the bile acid, such that the molecule exhibits a net charge of at least +1, the charge being contributed by the polyamine.
11. The method of claim 1 , wherein the aminosterol is modified to include one or more of the following:
(1) substitutions of the sulfate by a sulfonate, phosphate, carboxylate, or other anionic moiety chosen to circumvent metabolic removal of the sulfate moiety and oxidation of the cholesterol side chain;
(2) replacement of a hydroxyl group by a non-metabolizable polar substituent, such as a fluorine atom, to prevent its metabolic oxidation or conjugation; and
(3) substitution of various ring hydrogen atoms to prevent oxidative or reductive metabolism of the steroid ring system.
12. The method of claim 1 , wherein the aminosterol is a derivative of squalamine or natural aminosterol modified through medical chemistry to improve bio-distribution, ease of administration, metabolic stability, or any combination thereof.
13. The method of claim 1 , wherein the effective daily dosing amount is about 0.1 to about 20 mg/kg body weight.
14. The method of claim 1 , wherein the effective dose is established by defining the initial dose required to induce an Aminosterol-Induced GI Response, which is the initial dose required to stimulate a change in bowel activity, nausea, secretory diarrhea, or any combination thereof.
15. The method of claim 1 , wherein the squalamine or aminosterol is administered in combination with at least one additional active agent to achieve either an additive or synergistic effect.
16. The method of claim 15 , wherein the additional active agent is administered via a method selected from the group consisting of
(a) concomitantly;
(b) as an admixture;
(c) separately and simultaneously or concurrently; and
(d) separately and sequentially.
17. The method of claim 1 , wherein the oral dosage form is a liquid, capsule, or tablet designed to disintegrate in either the stomach, upper small intestine, or more distal portions of the intestine.
18. The method of claim 1 , wherein essentially no aminosterol is detected in the blood stream of the subject following oral administration.
19. The method of claim 1 , wherein the composition further comprises at least one pharmaceutically acceptable carrier.
20. The method of claim 1 , wherein the subject is human.
21. The method of claim 1 , wherein the at least one aminosterol is squalamine.