Abstract
The inhibitory impacts of RP 73401, a phosphodiesterase type 4 (PDE4) selective inhibitor of the second generation, versus rolipram, the prototypal PDE4 inhibitor, were evaluated and compared on cAMP phosphodiesterase (PDE) activity and contractility of the myometrium in nonpregnant and pregnant women. In enzymatic studies, RP 73401 and rolipram inhibited the cAMP PDE activity with significantly greater maximal efficiency in the myometrium of pregnant compared with nonpregnant women (75 versus 55%; P < .05). Although myometrial PDE4 presented a single class of interaction with RP 73401 [pD2 (−log [IC50]) = −8.2], it exhibited at least two classes of interaction with rolipram (pD2 = −8.2 and −5.6). In the myometrium of pregnant versus nonpregnant women, rolipram is significantly more efficacious in the concentration range >0.01 to 100 μM (P < .01), whereas no difference was observed for the concentration range <0.01 μM. In contractility studies, RP 73401 was equally effective in relaxing myometrial strips from both nonpregnant and pregnant women (pD2 = −8.8). Conversely, the ability of rolipram to inhibit contractions of the myometrium in pregnant women was significantly lower (pD2 = −7.2) compared with that in nonpregnant women (pD2 = −8.2; P < .01). Concomitantly, in the myometrium of pregnant women, a rise in immunoreactive PDE4B2 signal was detected, whereas the PDE4D3 signal was less intense. These results demonstrate that parallel to an accumulation of PDE4B2 isoform, a modification in the ratio of PDE4 conformers HPDE4 and LPDE4 (conformer that binds rolipram with high and low affinity, respectively) occurs in the myometrium of near-term pregnant women with an increase of LPDE4 functionally implicated in the contractile process. Such modifications provide a strong rationale to propose LPDE4 as potential pharmacologic targets for the design of new tocolytic treatments.
Footnotes
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Send reprint requests to: Marie-Josèphe Leroy, Unité INSERM 361, Pavillon Baudelocque, 123, boulevard Port-Royal, 75014 Paris, France. E-mail: leroy-zamia{at}cochin.inserm.fr
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1 A portion of this work was presented at the Gordon Research Conference on cyclic nucleotide phosphodiesterases, Waterville Valley, NH, 1999.
- Abbreviations:
- HPDE4
- PDE4 conformer that binds rolipram with high affinity
- PDE
- cyclic nucleotide phosphodiesterase
- PDE4
- phosphodiesterase type 4
- LPDE4
- PDE4 conformer that binds rolipram with low affinity
- PAGE
- polyacrylamide gel electrophoresis
- TBST
- tris-buffered saline/Tween 20
- DMSO
- dimethyl sulfoxide
- Received August 6, 1999.
- Accepted October 21, 1999.
- The American Society for Pharmacology and Experimental Therapeutics
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