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Heme oxygenase metabolites inhibit tubuloglomerular feedback (TGF)

Division of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan

Submitted 7 April 2008 ; accepted in final form 12 August 2008

Tubuloglomerular feedback (TGF) is the mechanism by which the macula densa (MD) senses increases in luminal NaCl concentration and sends a signal to constrict the afferent arteriole (Af-Art). The kidney expresses constitutively heme oxygenase-2 (HO-2) and low levels of HO-1. HOs release carbon monoxide (CO), biliverdin, and free iron. We hypothesized that renal HOs inhibit TGF via release of CO and biliverdin. Rabbit Af-Arts and attached MD were simultaneously microperfused in vitro. The TGF response was determined by measuring Af-Art diameter before and after increasing NaCl in the MD perfusate. When HO activity was inhibited by adding stannous mesoporphyrin (SnMP) to the MD perfusate, the TGF response increased from 2.1 ± 0.2 to 4.1 ± 0.4 µm (P = 0.003, control vs. SnMP, n = 7). When a CO-releasing molecule, (CORM-3; 50 µM), was added to the MD perfusate, the TGF response decreased by 41%, from 3.6 ± 0.3 to 2.1 ± 0.2 µm (P < 0.001, control vs. CORM-3, n = 12). When CORM-3 at 100 µM was added to the perfusate, it completely blocked the TGF response, from 4.2 ± 0.4 to –0.2 ± 0.3 µm (P < 0.001, control vs. CORM-3, n = 6). When biliverdin was added to the perfusate, the TGF response decreased by 79%, from 3.4 ± 0.3 to 0.7 ± 0.4 µm (P = 0.001, control vs. biliverdin, n = 6). The effects of SnMP and CORM-3 were not blocked by inhibition of nitric oxide synthase. We concluded that renal HO inhibits TGF probably via release of CO and biliverdin. HO regulation of TGF is a novel mechanism that could lead to a better understanding of the control of renal microcirculation and function.

carbon monoxide; biliverdin; afferent arteriole; macula densa