Destache C J, Pakiz C B, Dash A K, Larsen C
Department of Pharmacy Practice, Creighton University School of Pharmacy and Allied Health Professions, Omaha, Nebraska 68178, USA.
Pharmacotherapy. 1998 May-Jun;18(3):612-9.
Streptococcus pneumoniae is a common cause of meningitis. Nitric oxide (NO) has been implicated in causing cerebral edema. Modulating NO production in cerebrospinal fluid (CSF) may have a role in the treatment of bacterial meningitis. Experimental S. pneumoniae meningitis was induced in a rabbit model to determine CSF parameters and NO concentrations. An electrochemical probe in the CSF throughout the 7-hour experiment monitored NO concentrations. The animals had S. pneumoniae (10(5)) injected intracisternally and incubated for 1 hour. Cerebrospinal fluid 200-300 microl was obtained by intracisternal puncture at zero, 2, 4, and 7 hours after drug administration to measure glucose, protein, and lactic acid by standard chemical methods. White blood cell count was measured by hemocytometry. Three groups of five animals were used-control (C), ceftriaxone (CTX), and ceftriaxone plus dexamethasone (CTX+D). Ceftriaxone concentrations in CSF were obtained by microdialysis and analyzed by high-performance liquid chromatography. Mean (+/- SEM) CSF white blood cell count was significantly higher at 2 hours in the C group than in the other two groups (C 7307 +/- 1302, CTX 605 +/- 345, CTX+D 730 +/- 43/mm3, p<0.002). Ceftriaxone induced a significant rise in protein at 4 hours compared with the other groups (C 364 +/- 107, CTX 1158 +/- 797, CTX+D 365 +/- 100 mg/dl, p<0.02). Cerebrospinal fluid lactic acid was significantly different at 4 and 7 hours between C and CTX+D groups (4-hr C 8.0 +/- 2.2, CTX+D 2.0 +/- 0.4 mmol/L, p<0.05; 7-hr C 10.2 +/- 2.4, CTX+D 2.8 +/- 0.8 mmol/L, p<0.01). Median NO concentrations were significantly elevated in the control group compared with the other two groups (C 11.7, CTX 6.8, CTX+D 6.5 micro, p<0.02 C vs CTX, p<0.01 C vs CTX+D). Average (+/- SEM) NO concentrations were significantly higher in the C group at 4 hours (18.1 +/- 0.4, CTX 5.8 +/- 1.8 microM, p<0.05; CTX+D 11.5 +/- 4.0 microM, p>0.05), whereas they did not rise significantly until 7 hours in the CTX group (CTX 18.7 +/- 0.7, C 8.9 +/- 0.4 microM, p=0.055; CTX+D 8.1 +/- 2.2 microM, p<0.05). These results indicate that ceftriaxone with or without dexamethasone significantly decreases lactic acid concentrations and white cell penetration into the CSF in an experimental model of S. pneumoniae meningitis. In addition, ceftriaxone induced a significant elevation in CSF protein. Median NO production in the CSF was significantly attenuated by ceftriaxone.
肺炎链球菌是脑膜炎的常见病因。一氧化氮(NO)被认为与脑水肿的发生有关。调节脑脊液(CSF)中NO的产生可能在细菌性脑膜炎的治疗中发挥作用。在兔模型中诱导实验性肺炎链球菌脑膜炎,以确定脑脊液参数和NO浓度。在整个7小时的实验过程中,通过脑脊液中的电化学探头监测NO浓度。向动物脑池内注射肺炎链球菌(10⁵)并孵育1小时。在给药后0、2、4和7小时通过脑池穿刺获取200 - 300微升脑脊液,用标准化学方法测量葡萄糖、蛋白质和乳酸。通过血细胞计数法测量白细胞计数。使用三组,每组五只动物——对照组(C)、头孢曲松(CTX)组和头孢曲松加地塞米松(CTX + D)组。通过微透析获取脑脊液中的头孢曲松浓度,并通过高效液相色谱法进行分析。对照组在2小时时脑脊液白细胞计数平均值(±SEM)显著高于其他两组(C组7307±1302,CTX组605±345,CTX + D组730±43/mm³,p < 0.002)。与其他组相比,头孢曲松在4小时时导致蛋白质显著升高(C组364±107,CTX组1158±797,CTX + D组365±100mg/dl,p < 0.02)。C组和CTX + D组在4小时和7小时时脑脊液乳酸有显著差异(4小时时,C组8.0±2.2,CTX + D组2.0±0.4mmol/L,p < 0.05;7小时时,C组10.2±2.4,CTX + D组2.8±0.8mmol/L,p < 0.01)。与其他两组相比,对照组的NO浓度中位数显著升高(C组11.7,CTX组6.8,CTX + D组6.5微摩尔,C组与CTX组相比p < 0.02,C组与CTX + D组相比p < 0.01)。C组在4小时时平均(±SEM)NO浓度显著更高(18.1±0.4,CTX组5.8±1.8微摩尔,p < 0.05;CTX + D组11.5±4.0微摩尔,p > 0.05),而CTX组直到7小时NO浓度才显著升高(CTX组18.7±0.7,C组8.9±0.4微摩尔,p = 0.055;CTX + D组8.1±2.2微摩尔,p < 0.05)。这些结果表明,在实验性肺炎链球菌脑膜炎模型中,无论有无地塞米松,头孢曲松均能显著降低乳酸浓度以及白细胞进入脑脊液的数量。此外,头孢曲松使脑脊液蛋白质显著升高。头孢曲松显著降低了脑脊液中NO的产生中位数。