Department of Human Anatomy and Embryology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Department of Human Anatomy and Embryology, Faculty of Medicine, Helwan University, Cairo, Egypt.
Folia Morphol (Warsz). 2020;79(4):672-680. doi: 10.5603/FM.a2019.0127. Epub 2019 Nov 28.
Manganese (Mn) is widely used for industrial purposes and exposure to high levels of Mn may cause an irreversible brain disease. Propolis is a natural plant product; it acts as a powerful reactive oxygen species scavenger and improves the neurodegeneration process.
In this study 40 adult male albino rats were divided randomly into four groups 10 rats each: group I (control group), group II manganese chloride (MnCl2) received 10 mg/kg/day/orally for 4 weeks by intra-gastric tube, group III (propolis group) received 50 mg/kg/day/orally for 4 weeks by intra-gastric tube, and group IV (MnCl2 + propolis group) received the same doses with the same duration and route as in groups II and III. Rats were sacrificed after 24 h of last dose. The olfactory bulbs removed, the right bulb cut to be processed for haematoxylin and eosin, immunohistochemical staining and the left cut for electron microscopic studies.
Results revealed that rat olfactory bulb from MnCl2 group showed darkly stained mitral cells with dark pyknotic nuclei, some show pericellular spaces and vacuolation, dark apoptotic cells in granular cells, neuropil vacuolation and pyknotic astrocyte. Electron microscopic examination showed abnormal granular cell with irregular damaged nuclear membrane, rupture of myelin fibre. Mitral nerve cell with destructed nucleus, many cytoplasmic vacuoles, swollen rough endoplasmic reticulum, vacuolated mitochondria and neuropil were observed. Manganese chloride + propolis group showed improvement compared to MnCl2 group.
It was concluded that propolis can ameliorate the toxic changes of manganese chloride on rat olfactory bulb.
锰(Mn)广泛用于工业目的,接触高水平的 Mn 可能会导致不可逆的脑部疾病。蜂胶是一种天然植物产品;它作为一种强大的活性氧物质清除剂,可以改善神经退行性过程。
在这项研究中,40 只成年雄性白化大鼠被随机分为四组,每组 10 只:第 I 组(对照组)、第 II 组(氯化锰组)每天经胃管给予 10mg/kg,连续 4 周,第 III 组(蜂胶组)每天经胃管给予 50mg/kg,连续 4 周,第 IV 组(MnCl2+蜂胶组)给予相同剂量和相同途径与第 II 组和第 III 组相同。最后一次给药后 24 小时处死大鼠。取出嗅球,将右侧嗅球切成小块用于苏木精和伊红染色、免疫组织化学染色,将左侧嗅球切成小块用于电镜研究。
结果表明,MnCl2 组大鼠嗅球的颗粒细胞中出现深染的颗粒细胞,细胞核深染固缩,部分颗粒细胞出现胞质间隙和空泡化,颗粒细胞中出现暗凋亡细胞,神经胶质细胞固缩。电镜检查显示,颗粒细胞异常,核膜不规则损伤,髓鞘纤维破裂。嗅球内的嗅丝细胞出现核破坏,胞质内有许多空泡,内质网肿胀,线粒体空泡化,神经胶质细胞空泡化。MnCl2+蜂胶组与 MnCl2 组相比有所改善。
蜂胶可以改善氯化锰对大鼠嗅球的毒性变化。