Akgören N, Mathiesen C, Rubin I, Lauritzen M
Department of Medical Physiology, University of Copenhagen, Denmark.
Am J Physiol. 1997 Sep;273(3 Pt 2):H1166-76. doi: 10.1152/ajpheart.1997.273.3.H1166.
The purpose of the present study was to examine mechanisms of activity-dependent changes of cerebral blood flow (CBF) in rat cerebellar cortex by laser-Doppler flowmetry, using two synaptic inputs that excite different regions of the same target cell and with different synaptic strength. The apical part of Purkinje cells was activated by electrical stimulation of parallel fibers, whereas the cell soma and the proximal part of the dendritic tree were activated by climbing fibers using harmaline (40 mg/kg ip) or electrical stimulation of the inferior olive. Glass microelectrodes were used for recordings of field potentials and single-unit activity of Purkinje cells. CBF increases evoked by parallel fibers were most pronounced in the upper cortical layers. In contrast, climbing fiber stimulation increased CBF in the entire cortex. Inhibition of nitric oxide (NO) synthase activity by NG-nitro-L-arginine (L-NNA) or guanylate cyclase activity by 1H-[1,2,4(oxadiazolo)4,3-a]quinoxaline-1-one did not affect basal or harmaline-induced Purkinje cell activity but attenuated harmaline- and parallel fiber-evoked CBF increases by approximately 40-50%. Application of 8-(p-sulfophenyl)theophylline and adenosine deaminase reduced the harmaline-evoked CBF increase without any effect on the parallel fiber-evoked CBF response. The results suggest that CBF increases elicited by activation of Purkinje cells are partially mediated by the NO-guanosine 3',5'-cyclic monophosphate system independent of the input function but that adenosine contributes as well when climbing fibers are activated. This is the first demonstration of variations of coupling as a function of postsynaptic activity in the same cell.
本研究的目的是通过激光多普勒血流仪,利用两种能激发同一靶细胞不同区域且具有不同突触强度的突触输入,来研究大鼠小脑皮质中脑血流(CBF)的活动依赖性变化机制。通过电刺激平行纤维激活浦肯野细胞的顶端部分,而使用哈马灵(40mg/kg腹腔注射)或电刺激下橄榄核来激活细胞体和树突树的近端部分。玻璃微电极用于记录场电位和浦肯野细胞的单单位活动。平行纤维诱发的CBF增加在皮质上层最为明显。相比之下,攀缘纤维刺激使整个皮质的CBF增加。用NG-硝基-L-精氨酸(L-NNA)抑制一氧化氮(NO)合酶活性或用1H-[1,2,4(恶二唑)4,3-a]喹喔啉-1-酮抑制鸟苷酸环化酶活性,并不影响基础或哈马灵诱导的浦肯野细胞活动,但使哈马灵和平行纤维诱发的CBF增加减弱了约40%-50%。应用8-(对磺基苯基)茶碱和腺苷脱氨酶可减少哈马灵诱发的CBF增加,而对平行纤维诱发的CBF反应无任何影响。结果表明,浦肯野细胞激活引起的CBF增加部分由不依赖输入功能的NO-鸟苷3',5'-环磷酸系统介导,但当攀缘纤维被激活时腺苷也起作用。这是首次证明在同一细胞中耦合随突触后活动而变化。