Journal
HYPERTENSION
Volume 48, Issue 4, Pages 711-716Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/01.HYP.0000238442.33463.94
Keywords
kidney; cytokines; hypertension; endothelin
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Funding
- NHLBI NIH HHS [HL38499, HL078147, HL076145, HL51971] Funding Source: Medline
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The purpose of this study was to determine the role of interleukin (IL) 6 in mediating the increase in arterial pressure (AP) in response to chronic reductions in uterine perfusion pressure (RUPP) in pregnant rats. AP was higher in RUPP rats (138 +/- 1 mm Hg) than in normal pregnant (NP) rats (104 +/- 1 turn Hg). Serum IL-6 levels in the RUPP rats were 104.5 +/- 28.6 pg/mL as compared with 36.6 +/- 7.4 pg/mL in NP rats. To determine the long-term effects of a 2- to 3-fold elevation in plasma IL-6 on renal function and AP in pregnant rats, we infused IL-6 for 5 days (2.5 ng/day) in NP rats starting at day 14 of gestation. Five days later, serum IL-6 levels were 55.5 +/- 6.5 pg/mL in the control NP rats and 157.0 +/- 36.1 pg/mL in the IL-6-treated NP rats. AP was higher in the IL-6-treated NP rats (115 +/- 3 mm Hg) as compared with NP controls (101 +/- 1 turn Hg) at day 19 of gestation. Renal plasma flow and GFR were lower in the IL-6-treated NP rats than in the NP group. IL-6 increased plasma renin activity but did not affect endothelin in IL-6-treated NP rats. In contrast to the NP rats, IL-6 had no effect on AP or renal hemodynamics in virgin rats. In summary, these data indicate that plasma IL-6 is elevated in response to chronic reductions in uterine perfusion in pregnant rats and that a comparable elevation in plasma IL-6 increases AP and reduces renal function in pregnant rats.
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