Kang Ning, Ma Jie-hua, Zhou Xin, Fan Xiao-bo, Shang Xue-jun, Huang Yu-feng
College of Life Science, Nanjing Normal University, Nanjing, Jiangsu 210046, China.
Zhonghua Nan Ke Xue. 2011 May;17(5):422-6.
To explore the effects of L-carnitine (LC) on the apoptosis of spermatogenic cells and on the count and motility of epididymal sperm in rats with diabetes mellitus (DM).
Twenty-four SD rats (200-230 g) were randomly divided into a control group, a DM model group and an LC group. After the establishment of DM models in the latter two groups by injection of streptozotocin (STZ) at 65 mg/kg, the controls and DM models were treated intragastrically with physiological saline, while the rats in the LC group with LC at 300 mg/kg, all for 6 consecutive weeks. Twenty-four hours after the last administration, all the rats were killed for the detection of the count and motility of epididymal sperm and the apoptosis of spermatogenic cells.
The motilities of caput and cauda epididymal sperm were (53.7 +/- 1.8)% and (60.3 +/- 1.6)% in the LC group, significantly higher than in the DM model group ([32.2 +/- 2.0]% and [40.5 +/- 1.4]%, P < 0.05), but remarkably lower than in the control ([63.1 +/- 2.4 ]% and [68.9 +/- 1.3]%, P < 0.05). The count of cauda epididymal sperm was (25.5 +/- 1.1) x 10(6)/100 mg in the DM models, and was increased to (32.0 +/- 1.5) x 10(6)/100 mg after LC treatment (P < 0.05), but still markedly lower than in the controls ([37.8 +/- 1.1] x 10(6)/100 mg) (P < 0.05). The apoptosis rate of spermatogenic cells was (52.5 +/- 4.4)% in the DM model group, and it was reduced to (35.3 +/- 3.5)% after LC administration (P < 0.05), but still significantly higher than in the control group ([3.7 +/- 1.3]%) (P < 0.05).
Intragastrically gavage of LC at 300 mg/kg for 6 weeks increased the epididymal sperm count, improved sperm motility, and reduced the apoptosis of spermatogenic cells in rats with DM.
探讨左旋肉碱(LC)对糖尿病(DM)大鼠生精细胞凋亡及附睾精子计数和活力的影响。
将24只体重200 - 230 g的SD大鼠随机分为对照组、DM模型组和LC组。后两组通过腹腔注射链脲佐菌素(STZ)65 mg/kg建立DM模型,对照组和DM模型组灌胃生理盐水,LC组灌胃300 mg/kg LC,均连续给药6周。末次给药24小时后,处死所有大鼠,检测附睾精子计数和活力以及生精细胞凋亡情况。
LC组附睾头和附睾尾精子活力分别为(53.7±1.8)%和(60.3±1.6)%,显著高于DM模型组([32.2±2.0]%和[40.5±1.4]%,P < 0.05),但明显低于对照组([63.1±2.4]%和[68.9±1.3]%,P < 0.05)。DM模型组附睾尾精子计数为(25.5±1.1)×10⁶/100 mg,LC治疗后增加至(32.0±1.5)×10⁶/100 mg(P < 0.05),但仍显著低于对照组([37.8±1.1]×10⁶/100 mg)(P < 0.05)。DM模型组生精细胞凋亡率为(52.5±4.4)%,LC给药后降至(35.3±3.5)%(P < 0.05),但仍显著高于对照组([3.7±1.3]%)(P < 0.05)。
DM大鼠连续6周灌胃300 mg/kg LC可增加附睾精子计数,提高精子活力,减少生精细胞凋亡。