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Continuous inhibiti...
Continuous inhibition of 11 beta-hydroxysteroid dehydrogenase type I in adipose tissue leads to tachyphylaxis in humans and rats but not in mice
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- Gutierrez, P. Morentin (författare)
- AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England.
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- Gyte, A. (författare)
- AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England.
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- deSchoolmeester, J. (författare)
- AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England.
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- Ceuppens, P. (författare)
- AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England.
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- Swales, J. (författare)
- AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England.
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- Stacey, C. (författare)
- AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England.
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- Eriksson, Jan W. (författare)
- Uppsala universitet,Klinisk diabetologi och metabolism,AstraZeneca R&D, Molndal, Sweden.
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- Sjostrand, M. (författare)
- AstraZeneca R&D, Molndal, Sweden.
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- Nilsson, C. (författare)
- AstraZeneca R&D, Molndal, Sweden.
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- Leighton, B. (författare)
- AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England.
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AstraZeneca R&D, Mereside, Macclesfield SK10 4TG, Cheshire, England Klinisk diabetologi och metabolism (creator_code:org_t)
- 2015-10-08
- 2015
- Engelska.
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Ingår i: British Journal of Pharmacology. - : Wiley. - 0007-1188 .- 1476-5381. ; 172:20, s. 4806-4816
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https://bpspubs.onli...
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
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- Background and Purpose11-hydroxysteroid dehydrogenase type I (11-HSD1), a target for Type 2 diabetes mellitus, converts inactive glucocorticoids into bioactive forms, increasing tissue concentrations. We have compared the pharmacokinetic-pharmacodynamic (PK/PD) relationship of target inhibition after acute and repeat administration of inhibitors of 11-HSD1 activity in human, rat and mouse adipose tissue (AT). Experimental ApproachStudies included abdominally obese human volunteers, rats and mice. Two specific 11-HSD1 inhibitors (AZD8329 and COMPOUND-20) were administered as single oral doses or repeat daily doses for 7-9days. 11-HSD1 activity in AT was measured ex vivo by conversion of H-3-cortisone to H-3-cortisol. Key ResultsIn human and rat AT, inhibition of 11-HSD1 activity was lost after repeat dosing of AZD8329, compared with acute administration. Similarly, in rat AT, there was loss of inhibition of 11-HSD1 activity after repeat dosing with COMPOUND-20 with continuous drug cover, but effects were substantially reduced if a drug holiday' period was maintained daily. Inhibition of 11-HSD1 activity was not lost in mouse AT after continuous cover with COMPOUND-20 for 7days. Conclusions and ImplicationsHuman and rat AT, but not mouse AT, exhibited tachyphylaxis for inhibition of 11-HSD1 activity after repeat dosing. Translation of observed efficacy in murine disease models to human for 11-HSD1 inhibitors may be misleading. Investigators of the effects of 11-HSD1 inhibitors should confirm that desired levels of enzyme inhibition in AT can be maintained over time after repeat dosing and not rely on results following a single dose.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
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Gutierrez, P. Mo ...
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Gyte, A.
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deSchoolmeester, ...
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Ceuppens, P.
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Swales, J.
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Stacey, C.
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visa fler...
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Eriksson, Jan W.
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Sjostrand, M.
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Nilsson, C.
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Leighton, B.
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visa färre...
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