1.Ginkgo biloba extract protection in acute paraquat poisoning of rat lung tissue .
Jian-nin SU ; Xin-hai LI ; Hui DONG ; Hui CHEN ; Xian-li GUO ; Yin-ping TIAN ; Hen-wen SHI ; Shu-hua HUO
Chinese Journal of Industrial Hygiene and Occupational Diseases 2003;21(3):226-227
Acute Disease
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Animals
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Ginkgo biloba
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Glutathione
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analysis
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Lung
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drug effects
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metabolism
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pathology
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Malondialdehyde
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analysis
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Paraquat
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toxicity
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Phytotherapy
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Plant Extracts
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therapeutic use
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Poisoning
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drug therapy
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Rats
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Superoxide Dismutase
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analysis
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Treatment Outcome
2. Discussion on the Pathogenesis of Central Precocious Puberty
Na NI ; Xiang-Yang KONG ; Na NI ; Hen SU
Chinese Journal of Biochemistry and Molecular Biology 2021;37(6):727-732
Precocious puberty (PP) is a common childhood sexual dysplasia. Central precocious puberty (CPP) is a disease in which the hypothalamic-pituitary-gonadal (HPG) axis is activated in early age, leading to the early release of gonadotrophin releasing hormone, the early development of gonads, and the early onset of puberty. The occurrence of puberty is regulated by gene and environment. Current clinical studies have found that gain-of-function mutations in the KISS1 gene, and loss-of-function mutations in KISS1R (also named GPR54), MKRN3 and DLK1 genes are all important single-gene causes of central precocious puberty. KISS1 is a tumor metastasis suppressor gene. KISS1R codes a G protein-coupled receptor which with its ligand, kisspeptin, forms an excitatory neuroregulator system for GnRH secretion. They play a role in the upstream of the HPG axis. MKRN3 is a maternal-imprinted gene. DLK1 is a gene that regulates the growth of cell. They play a role in the downstream of HPG axis. Recently, the incidence of central precocious puberty has become higher and higher, which is related to the excessive exposure of environmental endocrine disruptors (EEDs) due to the continuous development of social economy. A number of investigations have found that children’s exposure to EEDs is significantly related to the incidence of precocious puberty. In humans, these EEDs also affect the metabolism of gut microbes. This paper aims to review the current studies on the single-gene pathogenesis, epigenetics, gut microbiota and environmental factors of central precocious puberty, so as to provide help for the treatment and prevention of this disease.