Dickerman J D, Chalmer B, Horner S R
Pediatr Res. 1980 Oct;14(10):1139-41. doi: 10.1203/00006450-198010000-00011.
In experiment 1, splenectomized mice exposed to 1 X 10(9) colony-forming units (cfu) of type 3 Streptococcus pneumoniae experienced no mortality when given 40,000 or 4,000 units of procaine penicillin IM starting 2 days before exposure and continuing for 4 days. On day 5, Bicillin was given once in the same dosages. In experiment 2, splenectomized mice exposed to 2.2 X 10(9) cfu were significantly protected by 400 but not 40 units of penicillin when compared to controls (P less than 0.005). In experiment 3, splenectomized mice exposed to 2.7 X 10(9) cfu were significantly protected when compared to controls if 4,000 units of procaine penicillin were given either 2 days postexposure for 2 days followed by 1 day of Bicillin in the same dosage or 4 days postexposure with the same schedule and dosage (P less than 0.005 and 0.01, respectively) but not 6 days postexposure.
在实验1中,接受1×10⁹个3型肺炎链球菌集落形成单位(cfu)的脾切除小鼠,在接触前2天开始给予40000或4000单位普鲁卡因青霉素肌肉注射,并持续4天,未出现死亡情况。在第5天,以相同剂量给予苄星青霉素一次。在实验2中,与对照组相比,接受2.2×10⁹ cfu的脾切除小鼠,给予400单位而非40单位青霉素时受到显著保护(P<0.005)。在实验3中,与对照组相比,接受2.7×10⁹ cfu的脾切除小鼠,如果在接触后2天给予4000单位普鲁卡因青霉素,持续2天,随后给予1天相同剂量的苄星青霉素,或者在接触后4天按相同方案和剂量给药(分别为P<0.005和0.01),则受到显著保护,但在接触后6天给药则无保护作用。