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Papillary plasma flow in rats. II. Hormonal control.
Pflugers Archiv : European Journal of Physiology
|August 1, 1983
Summary
Papillary plasma flow (PPF) is lower in male rats due to sex hormones and angiotensin II. Female rats have higher PPF, influenced by vasodilator prostaglandins. Captopril and indomethacin impact PPF by affecting these pathways.
Area of Science:
- Physiology
- Endocrinology
- Pharmacology
Background:
- Sex differences in papillary plasma flow (PPF) are significant, with males exhibiting lower flow than females.
- Hormonal and vasoactive factors are implicated in regulating PPF, but their specific roles remain unclear.
Purpose of the Study:
- To investigate the influence of sex hormones, angiotensin II (AII), prostaglandins (PGs), and pharmacological agents on papillary plasma flow (PPF) in Wistar rats.
- To elucidate the mechanisms underlying sex-based differences in PPF and the effects of captopril and indomethacin.
Main Methods:
- Papillary plasma flow (PPF) was quantified using the albumin accumulation technique in male and female Wistar rats.
- Experimental manipulations included castration, testosterone administration, indomethacin and captopril treatment, dehydration, and angiotensin II infusion.
- Measurements were taken under various physiological and pharmacological conditions to assess their impact on PPF.
Main Results:
- Male rats showed significantly lower PPF than females; castration increased PPF in males, while testosterone decreased it.
- Indomethacin reduced PPF in both sexes, whereas captopril increased it in males and maintained high levels in females, normalizing flow.
- Dehydration decreased PPF, an effect blunted by captopril. Angiotensin II infusion did not restore PPF in captopril-treated males, but AII combined with indomethacin did.
Conclusions:
- Male sex hormones and angiotensin II contribute to reduced papillary plasma flow (PPF) in male rats.
- Vasodilator prostaglandins play a crucial role in the higher PPF observed in female rats.
- Captopril exerts its vasodilatory effect on papillary circulation through both reduced AII formation and enhanced PG synthesis.