2006
DOI: 10.1016/j.yrtph.2006.06.003
|View full text |Cite
|
Sign up to set email alerts
|

Long-term safety of α-lipoic acid (ALA) consumption: A 2-year study

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
51
0
6

Year Published

2007
2007
2022
2022

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 91 publications
(60 citation statements)
references
References 29 publications
1
51
0
6
Order By: Relevance
“…Since the early 1990s, ·-lipoic acid has been used as a dietary supplement for humans, typically at doses in the range of 60-200 mg/day. In addition, the no observable adverse effect level (NOAEL) is considered to be 60 mg/kg wt/day (35). However, despite growing evidence of the benefits of ET or LA for the health and function of AD patients, there is little clinical evidence that supports the recommendations for ·-lipoic acid supplementation and ET guidelines in AD patients.…”
Section: Discussionmentioning
confidence: 99%
“…Since the early 1990s, ·-lipoic acid has been used as a dietary supplement for humans, typically at doses in the range of 60-200 mg/day. In addition, the no observable adverse effect level (NOAEL) is considered to be 60 mg/kg wt/day (35). However, despite growing evidence of the benefits of ET or LA for the health and function of AD patients, there is little clinical evidence that supports the recommendations for ·-lipoic acid supplementation and ET guidelines in AD patients.…”
Section: Discussionmentioning
confidence: 99%
“…Прегабалін -модулятор ноцицептивної та антиноцицептивної систем центральної дії з доведеною ефективністю щодо невропатичного болю, але з седативним ефектом (15%-25%), який обмежує титрацію дози. В дослідженнях, що вивчали дози α-ЛК 1200 мг на добу та більше, повідомлялося про такі побічні ефекти як нудота та блювання [39]. Проте в дослідженні безпеки в дозах 900 мг/день протягом 6 тижнів, а потім 1200 мг на день ще 6 тижнів, у поєднанні з пероральними цукрознижувальними засобами (метформіном, похідними сульфонілсечовини, глітазонами) та інсулінотерапією у хворих на ЦД 2 типу не спостерігалося серйозних побічних явищ чи відхилень біохімічних показників крові [40].…”
Section: патофізіологічні передумови та ефекти α-лкunclassified
“…Both in vitro and in vivo studies revealed that a new α-LA (DHL-HisZn, sodium zinc histidine dithiooctanamide) reduced serum levels of BUN and SCr, decreased MDA levels and ROS levels as well as alleviated the severity of kidney lesions (tubular cell necrosis, cytoplasmic vacuolation, hemorrhage and tubular dilatation) [27]. No acute, subacute and long-term toxicity by α-LA were found in both in vitro and in vivo studies [28,29]. LA was also shown to protect cisplatin-induced nephrotoxicity via oxidant defense system [29,34].…”
Section: Mechanisms Of La Cardioprotectionmentioning
confidence: 99%
“…In this context, LA has been shown to improve glucose and ascorbate handling, increase endothelial nitric oxide synthase activity, activate phase II detoxification via the transcription factor Nrf2 and lower expression of matrix metalloproteinase-9 and vascular cell adhesion molecule-1 through repression of nuclear factor-κB (NF-κB) [17]. In addition, animal studies have revealed that myocardial IRI [18,19,20,21,22,23] and renal IRI [24,25,26,27] could be protected by a naturally occurring cellular antioxidant LA, without being toxic to rats [28,29]. The mechanisms whereby LA exerts its protective effects are not entirely understood, but may be related to the phosphatidylinositol 3-kinase (PI3K)/Akt/Nrf2 pathway [23] and the PI3-kinase/Akt pathway, as ischemic preconditioning (IPC) reduces IRI of the rat liver via these pathways [30].…”
Section: Introductionmentioning
confidence: 99%