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Home: Papers of the Week
Annotation


Wang J, Ho L, Chen L, Zhao Z, Zhao W, Qian X, Humala N, Seror I, Bartholomew S, Rosendorff C, Pasinetti GM. Valsartan lowers brain beta-amyloid protein levels and improves spatial learning in a mouse model of Alzheimer disease. J Clin Invest. 2007 Nov;117(11):3393-402. PubMed Abstract

  
Comments on Paper and Primary News
  Primary News: Anti-hypertensives for AD?—Remembrances of NSAIDs Past

Comment by:  P.F. Jennings
Submitted 30 October 2007  |  Permalink Posted 30 October 2007

Perhaps the effect that is being seen is related to C-reactive protein. CRP is clearly implicated in Alzheimer's, and apparently valsartan reduces CRP.

Here are a few quotes to illustrate:

"Inflammation plays an important role in the pathogenesis of Alzheimer's disease.... [T]he level of systemic inflammation markers, particularly C-reactive protein and interleukin-6, can predict cognitive decline or dementia.” (1)

"Blood levels of CRP... are associated with higher risk of Alzheimer disease and cognitive decline during aging.” (2)

"C-reactive protein has been shown to co-deposit with C fragments in a number of disorders, including Alzheimer's disease..." (3)

"Angiotensin receptor blockers (ARBs) (valsartan, irbesartan, olmesartan, telmisartan) markedly reduce serum levels of CRP." (4)

References:
1. Dziedzic T. Systemic inflammatory markers and risk of dementia. Am J Alzheimers Dis Other Demen. 2006 Aug-Sep;21(4):258-62. Abstract

2. Finch CE, Morgan TE. Systemic inflammation, infection, ApoE alleles, and Alzheimer disease: a position paper. Curr Alzheimer Res. 2007 Apr;4(2):185-9. Abstract

3. Klegeris A, Singh EA, McGeer PL. Effects of C-reactive protein and pentosan polysulphate on human complement activation. Immunology. 2002 July; 106(3): 381–388. Abstract

4. Prasad K. C-reactive protein (CRP)-lowering agents. Cardiovasc Drug Rev. 2006 Spring;24(1):33-50. Abstract

View all comments by P.F. Jennings


  Comment by:  Boris Schmidt (Disclosure)
Submitted 7 November 2007  |  Permalink Posted 8 November 2007
  I recommend this paper

The analysis of the pleitropic effects of Valsartan is striking. The potential of a class effect amongst the sartan drug family should be investigated further. Several of the inactive compounds in the first assay round are not the real Valsartan competing agent: Losartan (a primary alcohol) is active as its acidic metabolite EXP3174; Candesartan Cilexitil is a prodrug, which requires metabolic activation.

Tasosartan, Telmisartan and Irbesartan lack a crucial acid moiety common to the other three.

References:
Schmidt B, Schieffer B. Angiotensin II AT1 Receptor Antagonists: Clinical Implications of Active Metabolites. J Med Chem. 2003 Jun 5;46(12):2261-70. Review. No abstract available. Abstract

View all comments by Boris Schmidt

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REAGENTS/MATERIAL:
Antibodies used in this study are:
mouse monoclonal anti-Aβ (6E10) (Signet); rabbit anti-Aβ oligomers (A11) (Biosource); rabbit anti-APP, full length (C8) (D. Selkoe, Brigham and Women’s Hospital, Boston); ELISA kit anti-total Aβ1-40 and total Aβ1-42 (Biosource); mouse monoclonal anti-APP (4G8) (Signet Covance); ELISA kit anti-α-secretase (R&D Systems); ELISA kit anti-β-secretase (R&D Systems); ELISA kit anti-γ-secretase (R&D Systems); rabbit anti-mouse NEP (Alpha Diagnostics International); rabbit anti-mouse IDE (Abcam); rabbit anti-actin (Sigma-Aldrich)

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