Citalopram and fluoxetine affects blood chemistry, hematology and brain serotonin in rats.

O A T Ebuehi, A A Akinbode, A R Erinfolami, A A Badaru, M A Yusuf, M O Ojajuni
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Abstract

Background: Depression is caused as a result of combination of genetic, biochemical, environmental, and psychological factors. Citalopram and fluoxetine are antidepressants which are considered the current standard for depression treatment. There are little or no reports as to whether these antidepressants affect blood chemistry and haematological parameters in humans.

Objective: The effects of citalopram and fluoxetine on blood chemistry, hematology and brain serotonin in rats were investigated.

Methods: Forty-five Sprague Dawley male albino rats (140.69 +/- 5.86g) were divided into 3 equal groups. The first group of rats were orally administered 2 ml of 0.25 mg/ml of citalopram, the second group was administered 2 ml of 0.25 mg/ml of fluoxetine and the third group was administered 2 ml of saline (0.89% NaCl) daily for 4 weeks. The body weights and feed intake of rats were recorded every other day throughout the duration of drug administration. Five rats from each group were sacrificed by cervical dislocation after 7, 14, 21 and 28 days of drug administration. Blood was taken intravenously into lithium heparinized tubes and brain excised. Blood chemistry and hematology were determined by auto analyzer, while brain serotonin levels were determined using High Performance Liquid Chromatography. Serum levels of creatinine, urea, albumin, protein, glucose and activities of aspartate aminotransferase (AST) and alanine amino transferase (ALT) were determined in rats administered citalopram, fluoxetine and saline. The packed cell volume, white blood cells, red blood cells and platelets of rats administered the respective drugs were determined.

Results: There was no significant (P > 0.01) difference in the mean body weight of rats administered fluoxetine, citalopram or saline for 2 weeks. There were no significant differences in the hematological parameters of rats. The results of the study showed that citalopram increase the body weight of rats in the third and fourth week and was reduced in fluoxetine administered rats. The drugs also affected brain serotonin level, lipid profile of rats and increased levels of albumin, glucose and activities of liver enzymes; aspartate aminotransferase and alanine aminotransferase.

Conclusion: Data of the study indicate that oral administration of citalopram and fluoxetine in rats for 4 weeks daily affected blood chemistry and do not affect haematological parameters.

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西酞普兰和氟西汀影响大鼠血液化学、血液学和脑血清素。
背景:抑郁症是遗传、生化、环境、心理等多种因素共同作用的结果。西酞普兰和氟西汀是抗抑郁药,被认为是目前治疗抑郁症的标准药物。关于这些抗抑郁药是否影响人类血液化学和血液学参数的报道很少或没有。目的:观察西酞普兰和氟西汀对大鼠血液化学、血液学及脑血清素的影响。方法:雄性白化大鼠45只(140.69±5.86g),随机分为3组。第一组大鼠每日口服0.25 mg/ml西酞普兰2 ml,第二组大鼠每日口服0.25 mg/ml氟西汀2 ml,第三组大鼠每日口服生理盐水2 ml (0.89% NaCl),连续4周。在给药期间每隔一天记录大鼠的体重和采食量。给药7、14、21、28 d后,每组取5只大鼠颈椎脱臼处死。血液被静脉注射到肝素化锂管中,大脑被切除。采用自动分析仪测定血液化学和血液学,高效液相色谱法测定脑血清素水平。测定西酞普兰、氟西汀和生理盐水给药大鼠血清肌酐、尿素、白蛋白、蛋白、葡萄糖水平和天冬氨酸转氨酶(AST)、丙氨酸氨基转移酶(ALT)活性。测定给药大鼠的堆积细胞体积、白细胞、红细胞和血小板的变化。结果:氟西汀、西酞普兰和生理盐水对大鼠平均体重的影响均无统计学意义(P > 0.01)。两组大鼠血液学指标无明显差异。研究结果表明,西酞普兰在第3周和第4周增加了大鼠的体重,而氟西汀则减少了大鼠的体重。这些药物还会影响大鼠的脑血清素水平、血脂水平,并增加白蛋白、葡萄糖水平和肝酶活性;谷草转氨酶和丙氨酸转氨酶。结论:本研究数据表明,大鼠口服西酞普兰和氟西汀4周,对血液化学有影响,对血液学参数无影响。
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