IN-VIVO PRODUCTION OF NITRIC-OXIDE CORRELATES WITH NMDA-INDUCED CEREBRAL HYPEREMIA IN NEWBORN SHEEP

被引:36
|
作者
NORTHINGTON, FJ
TOBIN, JR
KOEHLER, RC
TRAYSTMAN, RJ
机构
[1] JOHNS HOPKINS MED INST, DEPT PEDIAT, BALTIMORE, MD 21287 USA
[2] JOHNS HOPKINS MED INST, DEPT ANESTHESIOL CRIT CARE MED, BALTIMORE, MD 21287 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1995年 / 269卷 / 01期
关键词
CEREBRAL BLOOD FLOW; MICRODIALYSIS; CITRULLINE; NITRIC OXIDE SYNTHASE;
D O I
10.1152/ajpheart.1995.269.1.H215
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Stimulation of N-methyl-D-aspartate (NMDA) receptors in brain increases nitric oxide production in vitro. We tested the hypothesis that nitric oxide participates in the increase in local cerebral blood flow (CBF) caused by infusion of NMDA in anesthetized newborn sheep. We used the combined hydrogen clearance and microdialysis technique for simultaneous measurement of local CBF, infusion of drugs, and measurement of interstitial levels of L-[C-14]citrulline in the parietal cortex. Release of L-[C-14]citrulline into the dialysate during continuous infusion of L-[C-14]arginine was used as a marker of nitric oxide production in vivo. Citrulline recovery and CBF were measured hourly during a 4-h infusion of cerebrospinal fluid containing either 1) no additional drugs, 2) 1 mM NMDA, 3) 1 mM N-G-nitro-L-arginine methyl ester (L-NAME, a nitric oxide synthase inhibitor), 4) 1 mM NMDA + 1 mM L-NAME, 5) 0.1 mM 2-chloro-adenosine (adenosine receptor agonist), or 6) 0.1 mM 2-chloroadenosine + 1 mM L-NAME. At 240 min of perfusion, CBF (ml . min(-1). 100 g(-1); means +/- SE) was as follows: control 52 +/- 3, NMDA 116 +/- 11, L-NAME 32 +/- 5, NMDA + L-NAME 40 +/- 4, 2-chloroadenosine 201 +/- 63, and 2-chloroadenosine + L-NAME 129 +/- 18. Citrulline recovery (fmol/min) at 240 min of perfusion was as follows: control 38 +/- 12, NMDA 149 +/- 21, L-NAME 9 +/- 1, NMDA + L-NAME 39 +/- 5, 2-chloroadenosine 13 +/- 5, and 2-chloroadenosine + L-NAME 17 +/- 1. Infusion of NMDA increased CBF and L-[C-14]citrulline release, and these increases were inhibited by addition of L-NAME to the dialysate. In contrast, the cerebral vasodilator, 2-chloroadenosine, with or without L-NAME. increased CBF without an increase in L-[C-14]citrulline release, thereby demonstrating that the effect of L-NAME to block NMDA-mediated increases in CBF was specific and not due to generalized vasoparalysis. These results demonstrate that the local increase in CBF caused by stimulation of cortical NMDA receptors is dependent on production of nitric oxide. This study also demonstrates that microdialysate-measured conversion of L-[C-14]arginine to L-[C-14]citrulline is potentially useful as a marker of nitric oxide production in vivo.
引用
收藏
页码:H215 / H221
页数:7
相关论文
共 50 条
  • [41] CONTINUOUS NITRIC-OXIDE SYNTHESIS BY INDUCIBLE NITRIC-OXIDE SYNTHASE IN NORMAL HUMAN AIRWAY EPITHELIUM IN-VIVO
    GUO, FH
    DERAEVE, HR
    RICE, TW
    STUEHR, DJ
    THUNNISSEN, FBJM
    ERZURUM, SC
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) : 7809 - 7813
  • [42] EFFECT OF NITRIC-OXIDE SYNTHASE INHIBITION ON CEREBRAL HYPEREMIA PRODUCED BY HYPOGLYCEMIA IN PIGLETS
    ICHORD, RN
    KIRSCH, JR
    HELFAER, MA
    TRAYSTMAN, RJ
    FASEB JOURNAL, 1992, 6 (04): : A1462 - A1462
  • [43] METHEMOGLOBIN PRODUCTION BY NITRIC-OXIDE IN FRESH SHEEP BLOOD
    IWAMOTO, J
    KRASNEY, JA
    MORIN, FC
    RESPIRATION PHYSIOLOGY, 1994, 96 (2-3): : 273 - 283
  • [44] Effects of inhibition of neuronal nitric oxide synthase on NMDA-induced changes in cerebral blood flow and oxygen consumption
    Oak Chi
    Xia Liu
    Harvey R. Weiss
    Experimental Brain Research, 2003, 148 : 256 - 260
  • [45] GLUTAMATE-INDUCED CEREBRAL VASODILATION IS MEDIATED BY NITRIC-OXIDE (NO) THROUGH NMDA RECEPTORS IN PIGLETS
    MENG, W
    BUSIJA, D
    FASEB JOURNAL, 1994, 8 (04): : A27 - A27
  • [46] RAT CEREBRAL ARTERIOLAR RESPONSES TO CO2 IN-VIVO - ROLE OF ENDOTHELIUM AND NITRIC-OXIDE
    PELLIGRINO, DA
    WANG, Q
    KOENIG, HM
    ALBRECHT, RF
    ANESTHESIA AND ANALGESIA, 1994, 78 (02): : U183 - U183
  • [47] Effects of inhibition of neuronal nitric oxide synthase on NMDA-induced changes in cerebral blood flow and oxygen consumption
    Chi, OZ
    Liu, X
    Weiss, HR
    EXPERIMENTAL BRAIN RESEARCH, 2003, 148 (02) : 256 - 260
  • [48] SPINAL NITRIC-OXIDE SYNTHESIS INHIBITION BLOCKS NMDA-INDUCED THERMAL HYPERALGESIA AND PRODUCES ANTINOCICEPTION IN THE FORMALIN TEST IN RATS
    MALMBERG, AB
    YAKSH, TL
    PAIN, 1993, 54 (03) : 291 - 300
  • [49] NITRIC-OXIDE (NO) INHIBITION ATTENUATES MG-DEFICIENCY-INDUCED OXIDATIVE INJURY IN-VIVO
    MAK, IT
    STAFFORD, RE
    DICKENS, BF
    PHILLIPS, TM
    WEGLICKI, WB
    FASEB JOURNAL, 1995, 9 (03): : A31 - A31
  • [50] NMDA RECEPTORS INCREASE OH RADICALS IN-VIVO BY USING NITRIC-OXIDE SYNTHASE AND PROTEIN-KINASE-C
    HAMMER, B
    PARKER, WD
    BENNETT, JP
    NEUROREPORT, 1993, 5 (01) : 72 - 74