Graduate School of Human Development and Environment, Kobe University; 3-11, Tsurukabuto, Nada, Kobe 657-8501, Japan.
Comp Biochem Physiol A Mol Integr Physiol. 2011 Sep;160(1):94-9. doi: 10.1016/j.cbpa.2011.05.010. Epub 2011 May 23.
Multiple pathways from three types of multiple receptor sites to three types of metabotropic signal transduction pathways were investigated in the whole cell-clamp experiments using isolated labellar sugar receptor neurons (cells) of the adult blowfly, Phormia regina. First, the concentration-response curves of three types of sweet taste components specialized to multiple receptor sites were obtained: sucrose for the pyranose sites (P-sites), fructose for the furanose sites (F-sites), and l-valine for the alkyl sites (R-sites). Next, the effects of inhibitors such as 2', 5'-dideoxyadenosine on adenylyl cyclase in the cAMP pathway, LY 83583 on guanylyl cyclase in the cGMP pathway, and U-73122 on phospholipase C in the IP₃ pathway were examined. The results showed that all of the inhibitors affected each specific target in the second-messenger transduction pathways. The obtained results verified that the P-site corresponded to the cAMP, the F-site to the cGMP, and the R-site to the IP₃ transduction pathway, and that these three signal pathways did not have crossing points.
使用成年摇蚊的分离的唇瓣糖受体神经元(细胞),在全细胞钳位实验中研究了来自三种类型的多受体位点和三种类型的代谢型信号转导途径的多条途径。首先,获得了三种类型的甜味成分专门针对多种受体位点的浓度-反应曲线:吡喃糖位点(P-位点)的蔗糖、呋喃糖位点(F-位点)的果糖和烷基位点(R-位点)的 l-缬氨酸。接下来,研究了 2',5'-二脱氧腺苷等抑制剂对 cAMP 途径中腺苷酸环化酶、LY 83583 对 cGMP 途径中鸟苷酸环化酶和 U-73122 对 IP₃ 途径中磷脂酶 C 的影响。结果表明,所有抑制剂均影响第二信使转导途径中的每个特定靶标。所得结果证实 P-位点对应于 cAMP、F-位点对应于 cGMP,而 R-位点对应于 IP₃ 转导途径,并且这三个信号途径没有交叉点。