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Nitric oxide synthase in dog urethra: a histochemical and pharmacological analysis

机译:狗尿道中一氧化氮合酶的组织化学和药理学分析

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1 To examine the presence of nitric oxide synthase (NOS) activity in female dog urethra, pharmacological experiments were performed using electrical field stimulation (EFS), guanethidine, atropine, N~G-nitro-L-arginine methyl ester and L-arginine, NOS immunohistochemistry using specific anti-NOS antibody, and reduced nicotinamide adenine dinucleotide phosphate (NADPH) diaphorase staining were also performed. 2 EFS caused frequency-dependent contractions in all urethral preparations, but in the presence of guanethidine and atropine, EFS caused significant relaxation in the proximal urethra and was without effect on the distal urethra. 3 In the presence of guanethidine, atropine, and N~G-nitro-L-arginine methyl ester, small contractions to EFS were re-established in the proximal urethra, but not in the distal urethra. N~G-nitro-D-arginine methyl ester had no such effect. 4 In the presence of guanethidine, atropine, and N~G-nitro-L-arginine methyl ester, the addition of L-arginine, restored the EFS-elicited relaxant responses previously seen with guanethidine and atropine alone in the proximal urethra (at 30 Hz; 12.89 ± 5.27% to -2.44 ± 4.43%, mean + s.e., P < 0.05). D-Arginine had no such effect. 5 In the distal urethra, the addition of N~G-nitro-L-arginine methyl ester and then L-arginine had no effect on responses to EFS in preparations treated with guanethidine and atropine. 6 Sodium nitroprusside caused relaxation in both the proximal and distal urethra. The relaxant responses per cm~2 cross sectional area in the proximal and distal urethra were 1.23 ± 0.29, and 2.02 ± 0.54 g cm~(-2) cross sectional area (mean ± s.e.), respectively: there was no significant difference between them. 7 Both NOS and NADPH diaphorase-positive neurones were present in dog urethra, the densities of both being higher in the proximal urethra than in the distal urethra. 8 These results show that female dog urethra possesses NOS nerves and that endogenous NO may play a role in relaxation in the proximal but not the distal urethra.
机译:1为了检查雌性狗尿道中一氧化氮合酶(NOS)活性的存在,使用电场刺激(EFS),胍乙啶,阿托品,N〜G-硝基-L-精氨酸甲酯和L-精氨酸进行了药理实验,还进行了使用特异性抗NOS抗体的NOS免疫组化和减少的烟酰胺腺嘌呤二核苷酸磷酸(NADPH)心肌黄递酶染色。 2 EFS引起所有尿道制剂的频率依赖性收缩,但是在胍乙啶和阿托品存在的情况下,EFS导致尿道近端明显松弛,而对远端尿道无影响。 3在存在胍乙啶,阿托品和N〜G-硝基-L-精氨酸甲酯的情况下,在尿道近端重新建立了对EFS的小收缩,但在尿道远端没有重新收缩。 N〜G-硝基-D-精氨酸甲酯没有这种作用。 4在胍乙啶,阿托品和N〜G-硝基-L-精氨酸甲酯存在下,添加L-精氨酸可恢复先前在尿道近端单独用胍乙啶和阿托品观察到的EFS引起的松弛反应(30 Hz; 12.89±5.27%至-2.44±4.43%,平均值+ se,P <0.05)。 D-精氨酸没有这种作用。 5在尿道远端,先后加入N〜G-硝基-L-精氨酸甲酯和L-精氨酸对用胍乙啶和阿托品治疗的患者对EFS的反应没有影响。 6硝普钠引起尿道近端和远端的松弛。尿道近端和远端的每cm〜2截面积的松弛反应分别为1.23±0.29和2.02±0.54 g cm〜(-2)截面积(平均值±se):两者之间无显着差异。 7狗尿道中同时存在NOS和NADPH心肌黄递酶阳性神经元,尿道近端的密度均高于尿道远端。 8这些结果表明,雌性狗尿道具有NOS神经,内源性NO可能在近端尿道而不是远端尿道中发挥作用。

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