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New proposals for testing drugs with IKr-blocking activity to determine their teratogenic potential

Karlsson, Miriam (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Danielsson, Bengt R (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Nilsson, Mats F (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
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Danielsson, Christian (author)
Webster, William S (author)
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 (creator_code:org_t)
Bentham Science Publishers Ltd. 2007
2007
English.
In: Current pharmaceutical design. - : Bentham Science Publishers Ltd.. - 1381-6128 .- 1873-4286. ; 13:29, s. 2979-2988
  • Research review (peer-reviewed)
Abstract Subject headings
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  • Drugs blocking the potassium current IKr, either as an intended pharmacologic effect (eg antiarrhythmics dofetilide and almokalant) or as an unwanted side-effect (eg antihistamine astemizole, propulsive drug cisapride, antidepressive drugs and macrolide antibiotics) are potential human teratogens. It is the contention of this paper that the existing repeat dose regimen used in teratology studies to fulfil regulatory requirements, does not properly identify the teratogenic risk of these drugs. Results from conventional studies for dofetilide and almokalant showed high rates of postimplantation embryonic death with few malformed fetuses. For astemizole and cisapride only embryonic death was seen. These latter results were not considered important because they occurred either in the presence of maternal toxicity and/or at high doses. Subsequent studies have shown that IKr-blockers are highly teratogenic when administered on single gestational days (GD) during a sensitive period of rat pregnancy (GD 10-14) when they induce a high incidence of stage-specific malformations. This teratogenic activity of astemizole and cisapride was missed in the original teratology studies. Mechanistically IKr-blockers cause bradycardia and arrhythmia of the embryonic heart and while an embryo may be able to survive a single day exposure to a teratogenic dose, repeat dosing often leads to death of the embryo. With this review we suggest that new drugs identified at the preclinical stage of development as having IKr-blocking properties, should undergo more comprehensive teratology testing including single GD dosing and studies using embryo culture. This would further help identify and characterise their teratogenic potential.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

mice gestational days
Dofetilide
Teratogenicity
almokalant
Antidepressant Drugs
non-selective monoamine reuptake inhibitors
PHARMACY
FARMACI

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