Figure 1. Average nuclear magnetic resonance (NMR) metabolite determinations versus time during nitric oxide synthase (NOS) inhibitor pretreatment and hypoxia studies. The x axis depicts the time in minutes since the beginning of the NMR experiment. Times of hypoxia and recovery (reperfusion with oxygenated artificial cerebrospinal fluid [ACSF]) are indicated on the figure. Data are shown as the mean +/- SD, from experiments with 27 [micro sign]M 7-nitroindozole (7-NI) pretreatment (open circles), 27 [micro sign]M L-nitroarginine methyl ester (L-NAME) pretreatment (solid circles), 27 [micro sign]M L-nitroarginine (L-NOarg) pretreatment (solid triangles), and without NOS inhibitor pretreatment (open triangles); n = 3 for each of these groups. (A)[Greek small letter beta]-Adenosine triphosphate quantitations, and (B) phosphocreatine (phosphocreatine) quantitations. The y axis indicates the integrated NMR signal intensity normalized to its own control value (at t = 0). (C) The intracellular pH was obtained from [Greek small letter delta], the Pi-phosphocreatinechemical shift, using the same formula as in our previous studies. 

Figure 1. Average nuclear magnetic resonance (NMR) metabolite determinations versus time during nitric oxide synthase (NOS) inhibitor pretreatment and hypoxia studies. The x axis depicts the time in minutes since the beginning of the NMR experiment. Times of hypoxia and recovery (reperfusion with oxygenated artificial cerebrospinal fluid [ACSF]) are indicated on the figure. Data are shown as the mean +/- SD, from experiments with 27 [micro sign]M 7-nitroindozole (7-NI) pretreatment (open circles), 27 [micro sign]M L-nitroarginine methyl ester (L-NAME) pretreatment (solid circles), 27 [micro sign]M L-nitroarginine (L-NOarg) pretreatment (solid triangles), and without NOS inhibitor pretreatment (open triangles); n = 3 for each of these groups. (A)[Greek small letter beta]-Adenosine triphosphate quantitations, and (B) phosphocreatine (phosphocreatine) quantitations. The y axis indicates the integrated NMR signal intensity normalized to its own control value (at t = 0). (C) The intracellular pH was obtained from [Greek small letter delta], the Pi-phosphocreatinechemical shift, using the same formula as in our previous studies. 

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