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Pharmacological curve fitting to analyze cutaneous adrenergic responses

Producción científica: Articlerevisión exhaustiva

27 Citas (Scopus)

Resumen

Although dose-response curves are commonly used to describe in vivo cutaneous α-adrenergic responses, modeling parameters and analyses methods are not consistent across studies. The goal of the present investigation was to compare three analysis methods for in vivo cutaneous vasoconstriction studies using one reference data set. Eight women (22 ±1 yr, 24 ± 1 kg/m 2) were instrumented with three cutaneous microdialysis probes for progressive norepinephrine (NE) infusions (1 × 10 -8, 1 × 10 -6, 1 × 10 -5, 1 × 10 -4, and 1 × 10 -3 logM). NE was infused alone, co-infused with NG-monomethyl-L-arginine (L-NMMA, 10 mM) or Ketorolac tromethamine (KETO, 10 mM). For each probe, doseresponse curves were generated using three commonly reported analyses methods: 1) nonlinear modeling without data manipulation, 2) nonlinear modeling with data normalization and constraints, and 3) percent change from baseline without modeling. Not all data conformed to sigmoidal dose-response curves using analysis 1, whereas all subjects' curves were modeled using analysis 2. When analyzing only curves that fit the sigmoidal model, NE + KETO induced a leftward shift in ED 50 compared with NE alone with analyses 1 and 2 (F test, P < 0.05) but only tended to shift the response leftward with analysis 3 (repeated-measures ANOVA, P = 0.08). Neither maximal vasoconstrictor capacity (E max) in analysis 1 nor %change CVC change from baseline in analysis 3 were altered by blocking agents. In conclusion, although the overall detection of curve shifts and interpretation was similar between the two modeling methods of curve fitting, analysis 2 produced more sigmoidal curves.

Idioma originalEnglish
Páginas (desde-hasta)1703-1709
Número de páginas7
PublicaciónJournal of Applied Physiology
Volumen111
N.º6
DOI
EstadoPublished - dic 2011

Financiación

FinanciadoresNúmero del financiador
National Heart, Lung, and Blood Institute (NHLBI)R01HL071159

    ASJC Scopus subject areas

    • General Medicine

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