Angiotensin II-induced contraction is attenuated by nitric oxide in afferent arterioles from the nonclipped kidney in 2K1C

被引:22
|
作者
Helle, Frank [2 ]
Hultstrom, Michael [2 ]
Skogstrand, Trude [2 ]
Palm, Fredrik [3 ]
Iversen, Bjarne M. [1 ,2 ]
机构
[1] Haukeland Hosp, Renal Res Grp, N-5021 Bergen, Norway
[2] Univ Bergen, Inst Med, Renal Res Grp, Bergen, Norway
[3] Uppsala Univ, Dept Med Cell Biol, Uppsala, Sweden
关键词
two-kidney; one-clip; renovascular hypertension; ONE-CLIP HYPERTENSION; BILATERAL RENAL-FUNCTION; RENOVASCULAR HYPERTENSION; EFFERENT ARTERIOLES; TYPE-2; RECEPTOR; L-ARGININE; RATS; 2-KIDNEY; SYNTHASE; MICE;
D O I
10.1152/ajprenal.90518.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Helle F, Hultstrom M, Skogstrand T, Palm F, Iversen BM. Angiotensin II-induced contraction is attenuated by nitric oxide in afferent arterioles from the nonclipped kidney in 2K1C. Am J Physiol Renal Physiol 296: F78-F86, 2009. First published October 22, 2008; doi: 10.1152/ajprenal.90518.2008.-Two-kidney, one-clip (2K1C) is a model of renovascular hypertension where we previously found an exaggerated intracellular calcium (Ca-i(2+)) response to ANG II in isolated afferent arterioles (AAs) from the clipped kidney (Helle F, Vagnes OB, Iversen BM. Am J Physiol Renal Physiol 291: F140-F147, 2006). To test whether nitric oxide (NO) ameliorates the exaggerated ANG II response in 2K1C, we studied ANG II (10(-7) mol/l)-induced calcium signaling and contractility with or without the NO synthase (NOS) inhibitor N-G-nitro-L-arginine methyl ester (L-NAME). In AAs from the nonclipped kidney, L-NAME increased the ANG II-induced Ca-i(2+) response from 0.28 +/- 0.05 to 0.55 +/- 0.09 (fura 2, 340 nm/380 nm ratio) and increased contraction from 80 +/- 6 to 60 +/- 6% of baseline (P < 0.05). In vessels from sham and clipped kidneys, L-NAME had no effect. In diaminofluorescein-FM diacetate-loaded AAs from the nonclipped kidney, ANG II increased NO-derived fluorescence to 145 +/- 34% of baseline (P < 0.05 vs. sham), but not in vessels from the sham or clipped kidney. Endothelial NOS (eNOS) mRNA and ser-1177 phosphorylation were unchanged in both kidneys from 2K1C, while eNOS protein was reduced in the clipped kidney compared with sham. Cationic amino acid transferase-1 and 2 mRNAs were increased in 2K1C, indicating increased availability of L-arginine for NO synthesis, but counteracted by decreased scavenging of the eNOS inhibitor asymmetric dimethylarginine by dimethylarginine dimethylaminohydrolase 2. In conclusion, the Ca-i(2+) and contractile responses to ANG II are blunted by NO release in the nonclipped kidney. This may protect the nonclipped kidney from the hypertension and elevated ANG II levels in 2K1C.
引用
收藏
页码:F78 / F86
页数:9
相关论文
共 50 条
  • [1] AT1 receptors mediate angiotensin II-induced release of nitric oxide in afferent arterioles
    Patzak, A
    Lai, EY
    Mrowka, R
    Steege, A
    Persson, PB
    Persson, AEG
    KIDNEY INTERNATIONAL, 2004, 66 (05) : 1949 - 1958
  • [2] Nitric oxide counteracts angiotensin II induced contraction in efferent arterioles in mice
    Patzak, A
    Kleinmann, F
    Lai, EY
    Kupsch, E
    Skelweit, A
    Mrowka, R
    ACTA PHYSIOLOGICA SCANDINAVICA, 2004, 181 (04): : 439 - 444
  • [3] Angiotensin II activates the nitric oxide system via AT1 receptors in afferent arterioles
    Patzak, A
    Lai, FY
    Steege, A
    Mrowka, R
    Kupsch, E
    Persson, PB
    Persson, EG
    FASEB JOURNAL, 2004, 18 (04): : A289 - A289
  • [4] Regulation of intrarenal Angiotensin II in 2K1C rats
    Ingert, C
    Grima, M
    Coquard, C
    Steger, J
    Barthelmebs, M
    Imbs, JL
    JOURNAL OF HYPERTENSION, 2000, 18 : S14 - S14
  • [5] Endogenous nitric oxide and epoxyeicosatrienoic acids modulate angiotensin II-induced constriction in the rabbit afferent arteriole
    Kohagura, K
    Endo, Y
    Ito, O
    Arima, S
    Omata, K
    Ito, S
    ACTA PHYSIOLOGICA SCANDINAVICA, 2000, 168 (01): : 107 - 112
  • [6] Neuronal nitric oxide synthase-dependent afferent arteriolar function in angiotensin II-induced hypertension
    Ichihara, A
    Imig, JD
    Navar, LG
    HYPERTENSION, 1999, 33 (01) : 462 - 466
  • [7] Regulation of intrarenal angiotensin II in 2K1C rats.
    Ingert, C
    Grima, M
    Coquard, C
    Steger, J
    Barthelmebs, M
    Imbs, JL
    FASEB JOURNAL, 2000, 14 (08): : A1567 - A1567
  • [8] Neuronal nitric oxide synthase mediated regulation of afferent arteriolar diameter is reduced in angiotensin II-Induced hypertension
    Ichihara, A
    Imig, JD
    Inscho, EW
    Navar, LG
    HYPERTENSION, 1998, 32 (03) : 599 - 599
  • [9] Protective role of nitric oxide in the development of 2K1C Goldblatt hypertension
    Cervenka, L.
    Kopkan, L.
    Vaneckova, I.
    JOURNAL OF HYPERTENSION, 2007, 25 : S122 - S123
  • [10] Angiotensin (Ang) II AT-2-receptor-induced nitric oxide (NO) release sustains blood perfusion and oxygen availability in the post-clip kidney of two-kidney, one clip hypertensive (2K1C) rats
    Palm, Fredrik
    Connors, Stephanie G.
    Welch, William J.
    Wilcox, Christopher S.
    FASEB JOURNAL, 2007, 21 (05): : A497 - A498