尼克酰胺腺嘌呤二核苷酸

本实验采用还原型尼克酰胺腺嘌呤二核苷酸脱氢酶（NADPH-d）方法，观察扬子鳄食管颈段NOS阳性神经元和神经纤维的分布。

NADPH-diaphorase histochemistry was used to study the distribution of NOS-positive neurons and in the cervical esophagus in Alligator Sinensis .

还原型尼克酰胺腺嘌呤二核苷酸脱氢酶（NADPH－d）组化方法操作步骤中各种参数的选择

Determination of optimal conditions for various parameters in the protocol of histochemical technique on reduced nicotinamide adenine dinucleotide phosphate ( nadph ) - diaphorase

采用β-还原型尼克酰胺腺嘌呤二核苷酸磷酸-黄递酶（β-NADPH-d）组织化学技术研究不同剂量蛋白磷酸酶抑制剂岗田酸（OA）对嗜铬细胞瘤细胞株（PC12）一氧化氮合成酶（NOS）活性的影响。

Rat pheochromocytoma cells were cultured with different dose of okadaic acid ( OA ), and the activity of nitric oxide synthase ( NOS ) was detected by β NADPH diaphorase histochemistry .

本文采用还原型尼克酰胺腺嘌呤二核苷酸脱氢酶（NADPHd）组织化学和γ氨基丁酸（GABA）免疫组化双重染色相结合的方法，观察杏仁皮质核（Co）神经元内GABA与NADPHd的共存。

By using the method of NADPH-diaphorase ( NADPH-d ) histochemistry combined with GABA immunocytochemistry , we explored the coexistence of NADPH-d and GABA in the neurons of the rat cortical amygdaloid nucleus ( Co ) .

方法：用还原型尼克酰胺腺嘌呤二核苷酸磷酸脱氢酶-黄递酶（NADPH-d）组织化学法及图像分析，对不同年龄组翼腭神经节NOS阳性神经细胞进行观察。

Methods : The NOS positive cells in pterygopalatine ganglion of rats on development were observed by histochemical technique of reduced nicotinamide adenine dinucleotide phosphate diaphorase ( NADPH d ) activity and image analysis .

机体内有多种酶参与了ROS的生成，其中尼克酰胺腺嘌呤二核苷酸磷酸盐氧化酶（nicotinamideadeninedinucleotidephosphateoxidase，NADPHOxidase）目前被认为是血管内生成ROS的主要酶体。

There are many kinds of enzymes in vivo which participate in the formation of ROS , and nicotinamide adenine dinucleotide phosphate oxidase ( NADPH oxidase ) is now considered as the main enzyme of the endovascular ROS generation .

方法应用还原型尼克酰胺腺嘌呤二核苷酸磷酸脱氢酶（NADPH-d）组织化学方法观察孕14d起至生后14d大鼠端脑内NOS阳性神经元的形态和分布。

Methods NADPH-d histochemical method was used to investigate the micromorphology and distribution of NOS positive neurons in rat telencephalon from embryonic day 14 ( El4 ) to postnatal day 14 ( P14 ) .

应用光学显微镜下观察并计数脊髓后角Ⅰ～Ⅱ板层内尼克酰胺腺嘌呤二核苷酸-黄递酶阳性细胞数目；

NADPH-d positive cells in laminae ⅰ - ⅱ of spinal cord posterior horn were enumerated and observed with light microscope ;