Júnior Jairo Izidro Rossetti Navarro, Aires Rafaela, de Sousa Cutrim Thiago Antonio, Vasquez Elisardo Corral, Pereira Thiago Melo Costa, Campagnaro Bianca Prandi
Laboratory of Translational Physiology and Pharmacology, Pharmaceutical Sciences Graduate Program, Vila Velha University (UVV), R Mercurio s/n, Vila Velha, ES, 29102623, Brazil.
Federal Institute of Education, Science and Technology (IFES), Vila Velha, ES, Brazil.
Pharmacol Rep. 2025 Apr;77(2):463-473. doi: 10.1007/s43440-024-00690-6. Epub 2025 Jan 14.
The therapeutic targeting of the intestinal microbiota has gained increasing attention as a promising avenue for addressing mood disorders. This study aimed to assess the potential effect of supplementing standard pharmacological treatment with the probiotic kefir in patients with Major Depressive Disorder (MDD).
Thirty-eight female participants diagnosed with moderate MDD by the Hamilton Rating Scale for Depression (HAM-D) were selected to receive the probiotic kefir in conjunction with antidepressant therapy for 12 weeks. The participants were evaluated at baseline (T0) and 90 days after probiotic kefir supplementation (T90). HAM-D scores and blood samples were collected at both time points.
Probiotic supplementation significantly reduced MDD severity, as evidenced by lower HAM-D scores compared to baseline. Probiotic consumption for 90 days also significantly decreased interleukin-6 (IL-6), C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR) levels compared to baseline. However, probiotic kefir supplementation did not significantly affect serum serotonin levels. Additionally, after 90 days of probiotic consumption, insulin and morning cortisol levels were significantly reduced. In contrast, no significant changes were observed in serum levels of prolactin, vitamin D, and afternoon cortisol.
This study provides valuable insights into the potential benefits of probiotics, specifically kefir, as adjunctive therapy for female patients with MDD. The findings highlight promising results in ameliorating depressive symptoms and modulating inflammatory and hormonal markers.
肠道微生物群的治疗靶向作为解决情绪障碍的一种有前景的途径,已受到越来越多的关注。本研究旨在评估用益生菌开菲尔补充标准药物治疗对重度抑郁症(MDD)患者的潜在效果。
选取38名通过汉密尔顿抑郁量表(HAM-D)诊断为中度MDD的女性参与者,接受益生菌开菲尔联合抗抑郁治疗12周。在基线(T0)和补充益生菌开菲尔90天后(T90)对参与者进行评估。在两个时间点收集HAM-D评分和血样。
补充益生菌显著降低了MDD的严重程度,与基线相比HAM-D评分更低证明了这一点。与基线相比,食用90天益生菌还显著降低了白细胞介素-6(IL-6)、C反应蛋白(CRP)和红细胞沉降率(ESR)水平。然而,补充益生菌开菲尔对血清5-羟色胺水平没有显著影响。此外,食用90天益生菌后,胰岛素和早晨皮质醇水平显著降低。相比之下,催乳素、维生素D和下午皮质醇的血清水平没有观察到显著变化。
本研究为益生菌,特别是开菲尔,作为MDD女性患者辅助治疗的潜在益处提供了有价值的见解。研究结果突出了在改善抑郁症状以及调节炎症和激素标志物方面的有前景的结果。