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ALA question

Bramil

New member
Can ALA be used instead of slin while on HGH?

I have read some reports on the subject. but would like a confim on this.
 
Well isnt ALA also used for type(2) diabetics?

which for the regular person using HGH. this would suffice.
but before making plans. I would like someone to confirm.
 
I am pretty sure that ALA is used for type 2 diabetes but it is administered I.V. not orally. Not 100% sure on this though. I came across a study on it a while back. i will see If I can find it.
 
Gluccophage is

used for type II diabetics and insulin resistance, ALA can be used in its place although there haven't been any conclusive tests that I know of, and as far as doseages I use 500mg a day. My wife on the other hand is insulin resistant and has 2000mg of gluccophage perscribed to her by an endocrinologist. That's about all I can tell ya..
 
macrophage69alpha said:
ala is a good supplement.. it will increase insulin sensitivity and is a great anti-oxident

Thanks Macro.


gethard1: I did at first want to use gluccophage but for me hard to get too. while ALA i can get readily.
 
Oral administration of RAC-alpha-lipoic acid modulates insulin sensitivity in patients with type-2 diabetes mellitus: a placebo-controlled pilot trial.

Jacob S, Ruus P, Hermann R, Tritschler HJ, Maerker E, Renn W, Augustin HJ, Dietze GJ, Rett K.

Hypertension and Diabetes Research Unit, Max Grundig Clinic, Buhl and City Hospital, Baden-Baden, Germany. [email protected]

Alpha-lipoic acid (ALA), a naturally occuring compound and a radical scavenger was shown to enhance glucose transport and utilization in different experimental and animal models. Clinical studies described an increase of insulin sensitivity after acute and short-term (10 d) parenteral administration of ALA. The effects of a 4-week oral treatment with alpha-lipoic acid were evaluated in a placebo-controlled, multicenter pilot study to determine see whether oral treatment also improves insulin sensitivity. Seventy-four patients with type-2 diabetes were randomized to either placebo (n = 19); or active treatment in various doses of 600 mg once daily (n = 19), twice daily (1200 mg; n = 18), or thrice daily (1800 mg; n = 18) alpha-lipoic acid. An isoglycemic glucose-clamp was done on days 0 (pre) and 29 (post). In this explorative study, analysis was done according to the number of subjects showing an improvement of insulin sensitivity after treatment. Furthermore, the effects of active vs. placebo treatment on insulin sensitivity was compared. All four groups were comparable and had a similar degree of hyperglycemia and insulin sensitivity at baseline. When compared to placebo, significantly more subjects had an increase in insulin-stimulated glucose disposal (MCR) after ALA treatment in each group. As there was no dose effect seen in the three different alpha-lipoic acid groups, all subjects receiving ALA were combined in the "active" group and then compared to placebo. This revealed significantly different changes in MCR after treatment (+27% vs. placebo; p < .01). This placebo-controlled explorative study confirms previous observations of an increase of insulin sensitivity in type-2 diabetes after acute and chronic intravenous administration of ALA. The results suggest that oral administration of alpha-lipoic acid can improve insulin sensitivity in patients with type-2 diabetes. The encouraging findings of this pilot trial need to be substantiated by further investigations.
 
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