Enhanced neutrophil superoxide anion production and its modification by beraprost sodium in spontaneously hypertensive rats

To clarify the function of polymorphonuclear leukocytes (PMN) in spontaneously hypertensive rats (SHR) and the effect of beraprost sodium (BS) on these functions, we examined superoxide anion (O2−) production and adherent activity by PMN, as well as modification of these functions by BS ex vivo and in vitro. In study 1, we measured PMN functions in 4-week-old SHR and Wistar-Kyoto (WKY) rats. In study 2 (ex vivo), 14-week-old SHR received vehicle (n = 6) and BS (30 μg/kg/day [n = 6] and 100 μg/kg/day [n = 7]) once daily for 4 weeks. In study 3 (in vitro), PMN from 18-week-old SHR were incubated with BS (0.1 and 1 μmol/L) and theophylline (200 μmol/L), which is reported to inhibit the PMN O2− production. Systolic blood pressure, platelet counts, and PMN O2− production stimulated by phorbol ester myristate acetate were significantly elevated in 4-week-old SHR compared with WKY (P< .05). Beraprost sodium decreased the ex vivo PMN O2− production, serum superoxide dismutase activity, and platelet counts (P< .05); however, BS did not reduce the in vitro PMN O2− production. These data support our hypothesis that the enhanced PMN function contributes to the cardiovascular damages during the early phase of SHR, and that BS has merit for preventing the O2− related organ damages in this model.