Vasopressin Stimulates Urinary Kallikrein Excretion in the Isolated Erythrocyte-Perfused Rat Kidney

Abstract

We have found that arginine vasopressin (AVP) (10 pg/ml) stimulates urinary kallikrein in the isolated erythrocyte perfused rat kidney. (In this model, perfusate flow rate approximates blood flow rates in vivo and morphology is normal.) Urinary kallikrein excretion rose from 6.9 ± 0.8 to 14.9 ± 2.4 ng/min 20 min after the addition of AVP to the perfusate, and then fell towards baseline levels over the next 30 min. 1-Desamino-8-D-AVP (8 pg/ml) caused a comparable increase in kallikrein excretion. Prostaglandin synthesis inhibition with indomethacin did not alter the stimulatory effect of AVP on kallikrein excretion. Parathyroid hormone 1–34 (144 ng/ml) and calcitonin (102 ng/ml) also increased urinary kallikrein. Kallikrein excretion rose from 9.1 ± 2.0 to 24 ± 4.5 ng/min in response to calcitonin and from 8.3 ± 1.6 to 43.7 ± 3.4 ng/min following the addition of parathyroid hormone to the perfusate. Kallikrein was found to accumulate in the perfusate in a linear fashion. Based on the slope of the relationship between perfusate kallikrein and time, the rate of release of kallikrein into the perfusate was estimated to be 0.79 ng/min in control kidneys. The rate of release of kallikrein into the perfusate in kidneys treated with AVP was the same (0.74 ng/min). Thus while kallikrein is released into the perfusate, this process is not influenced by AVP. In conclusion, AVP stimulates release of kallikrein into the urine (but not the perfusate) independently of systemic events. The effect of AVP is not mediated by prostaglandins. This effect of AVP is mediated via stimulation of the V2 receptor and also occurs in response to two other hormones (calcitonin and parathyroid hormone) that are known to stimulate adenyl cyclase in the rat distal nephron.

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“…Water-loaded rats administered ADH also increased their urinary kallikrein . Increased excretion of urinary kallikrein with arginine vasopressin was observed in isolated erythrocyte-perfused rat kidney (Stephens et al, 1988); cortical slices from rat, monkey, and human kidney (Grenfell et al, 1988); and collagenase-dispersed rat and human renal cortical cells (effective by 10-8-9 M of arginine vasopressin) (Marshall et al, 1992). Increased excretion of urinary kallikrein with arginine vasopressin was observed in isolated erythrocyte-perfused rat kidney (Stephens et al, 1988); cortical slices from rat, monkey, and human kidney (Grenfell et al, 1988); and collagenase-dispersed rat and human renal cortical cells (effective by 10-8-9 M of arginine vasopressin) (Marshall et al, 1992).…”