Department of Anatomical Sciences, Medical School, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Animal Model Exp Med. 2022 Apr;5(2):133-140. doi: 10.1002/ame2.12217. Epub 2022 Mar 11.
Nicotine administration can generate severe oxidative stress and lipid peroxidation. Royal jelly, with its antioxidant properties, acts as a scavenger of reactive oxygen species. This study describes the apitherapy effects of royal jelly on testicular damage following nicotine administration.
Forty-eight male BALB/c mice were divided into 8 groups (n = 6): saline, 3 different doses of royal jelly (100, 150, and 200 mg/kg body weight (BW) per day), nicotine (1.5 mg/kg), and 3 different groups of Nic + Roy (1.5 mg/kg of Nic + 100, 150, and 200 mg/kg BW per day of royal jelly). Nicotine was administrated intraperitoneally, and royal jelly was prescribed orally for 10 consecutive days. Serum levels of hormones (testosterone, luteinizing hormone, and follicle-stimulating hormone), total antioxidant capacity, nitric oxide (NO) status, malondialdehyde levels, sperm DNA fragmentation, sperm parameters, histopathological changes (H&E staining), immunohistochemistry against apoptotic proteins, and gene expression of Bcl-2, p53, Caspase-3, and Nrf2 (real-time PCR) were assessed to evaluate the molecular and histological changes.
Hormone levels, sperm parameters, and status of antioxidants were decreased significantly (p < .05) following nicotine administration. Moreover, royal jelly treatment normalized hormonal and antioxidant characteristics, decreased apoptotic gene expression, increased Nfr2 gene expression, and restored histopathological alteration to the physiological status significantly (p < .05).
Royal jelly upregulates the antioxidant status, inhibits the mitochondrial-dependent apoptosis pathway, and increases the rate of proliferation. This therapeutic agent effectively protected the testis against nicotine-associated damages by antioxidant and anti-apoptotic effects.
尼古丁给药会产生严重的氧化应激和脂质过氧化。蜂王浆具有抗氧化特性,可作为活性氧的清除剂。本研究描述了蜂王浆对尼古丁给药后睾丸损伤的蜂疗作用。
将 48 只雄性 BALB/c 小鼠分为 8 组(n=6):生理盐水、蜂王浆(100、150 和 200mg/kg 体重/天)3 个不同剂量组、尼古丁(1.5mg/kg)和尼古丁+蜂王浆(1.5mg/kg 尼古丁+100、150 和 200mg/kg 体重/天蜂王浆)3 个不同组。尼古丁经腹腔给药,蜂王浆经口连续 10 天给药。评估血清激素(睾酮、黄体生成素和卵泡刺激素)、总抗氧化能力、一氧化氮(NO)状态、丙二醛水平、精子 DNA 碎片化、精子参数、组织病理学变化(H&E 染色)、凋亡蛋白免疫组化以及 Bcl-2、p53、Caspase-3 和 Nrf2 基因表达(实时 PCR),以评估分子和组织学变化。
尼古丁给药后,激素水平、精子参数和抗氧化状态显著降低(p<0.05)。此外,蜂王浆治疗可使激素和抗氧化特征正常化,降低凋亡基因表达,增加 Nfr2 基因表达,并使组织病理学改变显著恢复到生理状态(p<0.05)。
蜂王浆上调抗氧化状态,抑制线粒体依赖性凋亡途径,增加增殖率。这种治疗剂通过抗氧化和抗凋亡作用,有效保护睾丸免受尼古丁相关损伤。