Orthostatic Responses to Nitric Oxide Synthase Inhibition in Persons With Tetraplegia

被引:10
|
作者
Wecht, Jill M. [1 ,2 ,3 ]
Radulovic, Miroslav [1 ]
LaFountaine, Michael F. [1 ]
Rosado-Rivera, Dwindally [1 ]
Zhang, Run-Lin [1 ]
Bauman, William A. [1 ,2 ,3 ]
机构
[1] James J Peters VA Med Ctr, Ctr Excellence Med Consequences Spinal Cord Injur, Bronx, NY 10468 USA
[2] Mt Sinai Sch Med, Dept Rehabil Med, New York, NY USA
[3] Mt Sinai Sch Med, Dept Med, New York, NY USA
来源
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION | 2009年 / 90卷 / 08期
关键词
Hypotension; orthostatic; Rehabilitation; Spinal cord injuries; Tilt-table test; SPINAL-CORD-INJURY; SYMPATHETIC PREGANGLIONIC NEURONS; PLASMA-RENIN ACTIVITY; SIMULATED MICROGRAVITY; MYOCARDIAL-INFARCTION; BLOOD-PRESSURE; HYPOTENSION; MECHANISMS; RISK; EXPRESSION;
D O I
10.1016/j.apmr.2009.02.004
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Wecht JM, Radulovic M, LaFountaine MF, Rosado-Rivera D, Zhang R-L, Bauman WA. Orthostatic responses to nitric oxide synthase inhibition in persons with tetraplegia. Arch Phys Med Rehabil 2009;90:1428-34. Objectives: To determine the effects of 1.0mg/kg nitro-L-arginine methyl ester (L-NAME) on orthostatic mean arterial pressure (MAP), serum aldosterone, and plasma renin concentrations in persons with chronic tetraplegia compared with nonspinal cord-injured controls. Design: Prospective placebo-controlled intervention study. Setting: James J. Peters Veterans Affairs Medical Center. Participants: Patients (n=5) with tetraplegia and controls (n=7) participated. The groups were matched for age, height, and weight; the average duration of injury in the tetraplegia group was 22 +/- 14 years. Intervention: Subjects with tetraplegia visited the laboratory twice, receiving placebo on day 1 and L-NAME (1.0mg/kg) on day 2. The agents were infused via an intravenous catheter over 60 minutes with the patient in the supine position. Data were collected during the infusion and then during head-up tilt to 45 degrees for 30 minutes. Control subjects visited the laboratory once for placebo infusion and the head-up tilt maneuver. Main Outcome Measure: Orthostatic MAP. Results: Orthostatic MAP was reduced after placebo infusion in subjects with tetraplegia compared with controls (69 +/- 11 vs 89 +/- 9mmHg, respectively; P <.01) and compared with L-NAME infusion (90 +/- 16mmHg; P <.01). Orthostatic MAP did not differ when comparing the tetraplegia group with controls after L-NAME infusion. Orthostatic aldosterone levels were increased after placebo compared with L-NAME infusion in persons with tetraplegia; plasma renin levels did not differ among the groups. Conclusions: These data suggest that nitric oxide synthase inhibition may have clinical potential for treatment of orthostatic hypotension in persons with chronic tetraplegia.
引用
收藏
页码:1428 / 1434
页数:7
相关论文
共 50 条
  • [41] Influence of nitric oxide synthase inhibition on the motility and sensitivity of distal colon in man
    Corsetti, M.
    Vos, R.
    Gevers, A.
    Demedts, I.
    Janssens, J.
    Tack, J.
    NEUROGASTROENTEROLOGY AND MOTILITY, 2013, 25 (04) : e256 - e262
  • [42] Role of nitric oxide synthase inhibition in the acute hypertensive response to intracerebroventricular cadmium
    Demontis, MP
    Varoni, MV
    Volpe, AR
    Emanueli, C
    Madeddu, P
    BRITISH JOURNAL OF PHARMACOLOGY, 1998, 123 (01) : 129 - 135
  • [43] Cardiovascular effects of chronic nitric oxide synthase inhibition in genetically hypertensive rats
    Orange, SJ
    Ledingham, JM
    Laverty, R
    CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2000, 27 (07) : 488 - 493
  • [44] Inhibition of nitric oxide synthase with pyrazole-1-carboxamidine and related compounds
    Southan, GJ
    Gauld, D
    Lubeskie, A
    Zingarelli, B
    Cuzzocrea, S
    Salzman, AL
    Szabo, C
    Wolff, DJ
    BIOCHEMICAL PHARMACOLOGY, 1997, 54 (03) : 409 - 417
  • [45] Roles of Neuronal Nitric Oxide Synthase and Inducible Nitric Oxide Synthase in Intestinal Transplantation of Rats
    Li, X. L.
    Zou, X. M.
    Nie, G.
    Song, M. L.
    Li, G.
    TRANSPLANTATION PROCEEDINGS, 2013, 45 (06) : 2497 - 2501
  • [46] In vitro modulation of inducible nitric oxide synthase gene expression and nitric oxide synthesis by procalcitonin
    Hoffmann, G
    Totzke, G
    Seibel, M
    Smolny, M
    Wiedermann, FJ
    Schobersberger, W
    CRITICAL CARE MEDICINE, 2001, 29 (01) : 112 - 116
  • [47] Nitric oxide synthase isoforms and the effect of their inhibition on meiotic maturation of porcine oocytes
    Chmelikova, Eva
    Jeseta, Michal
    Sedmikova, Marketa
    Petr, Jaroslav
    Tumova, Lenka
    Kott, Tomas
    Lipovova, Petra
    Jilek, Frantisek
    ZYGOTE, 2010, 18 (03) : 235 - 244
  • [48] Endothelial nitric oxide synthase inhibition triggers inflammatory responses in the brain of male rats exposed to ischemia-reperfusion injury
    Greco, Rosaria
    Demartini, Chiara
    Zanaboni, Anna Maria
    Blandini, Fabio
    Amantea, Diana
    Tassorelli, Cristina
    JOURNAL OF NEUROSCIENCE RESEARCH, 2018, 96 (01) : 151 - 159
  • [49] Inducible nitric oxide synthase-derived extracellular nitric oxide flux regulates proinflammatory responses at the single cell level
    Somasundaram, Veena
    Gilmore, Anne C.
    Basudhar, Debashree
    Palmieri, Erika Mariana
    Scheiblin, David A.
    Heinz, William F.
    Cheng, Robert. Y. S.
    Ridnour, Lisa A.
    Altan-Bonnet, Gregoire
    Lockett, Stephen J.
    McVicar, Daniel W.
    Wink, David A.
    REDOX BIOLOGY, 2020, 28
  • [50] Nitric oxide synthase inhibitors with cardiovascular therapeutic potential
    Hansen, DW
    EXPERT OPINION ON THERAPEUTIC PATENTS, 1999, 9 (05) : 537 - 547