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Objective:To study the impact of excessive iodide intake during pregnancy and lactation on lipid metabolism in offspring male rats.Methods:Forty-eight six-week-old Wistar rats (half male and half female) were fed adaptively for one week. The cage was closed according to the ratio of male and female 1∶1. The pregnant rats were divided into two groups according to their weight (220-240 g) by random number table. (1) 10 times high iodine (10 HI) intake during pregnancy and lactation until the postnatal day 21 (PN21) of their offspring: pregnant rats were divided into normal iodine group (NI group, drinking deionized water), 10 HI group (drinking potassium iodide solution with iodine content of 2 250 μg/L). Breast milk was used to feed the offspring rats to PN21, and the offspring male rats were taken as the research subjects, with 6 rats in each group. (2) 100 times high iodine (100 HI) intake during pregnancy and lactation to the offspring postnatal day 120 (PN120): pregnant rats were divided into NI group (drinking deionized water) and 100 HI group (drinking potassium iodide solution with iodine content of 24 750 μg/L). After feeding the offspring rats with breast milk until PN21, the offspring were continued to drink potassium iodide solution with the same iodine content as the mother's to PN120. The offspring male rats were taken as the research subjects, with 6 rats in each group. The levels of free triiodothyronine (FT 3), free thyroxine (FT 4), thyrotropin (TSH) in serum, low-density lipoprotein cholesterol (LDL-C), triglyceride (TG) and total cholesterol (TC) in serum and liver tissue homogenates were measured by enzyme-linked immunosorbent assay (ELISA). The mRNA expression of cholesterol 7α-hydroxylase (CYP7A), low-density lipoprotein receptors (LDLR), sterol regulatory element-binding protein (SREBP)-1c, malic enzyme (ME) and thyroid hormone receptor β (TRβ) in the liver tissue were measured by real-time quantitative PCR. Results:(1) Effects of 10 HI intake during pregnancy and lactation on PN21 offspring male rats: compared with NI and 10 HI groups, the serum FT 3 [(7.53 ± 0.74), (8.88 ± 0.99) pmol/L], FT 4 [(5.58 ± 0.56), (7.68 ± 0.30) pmol/L], TSH levels [(16.69 ± 1.05), (14.49 ± 0.16) ng/ml] of offspring male rats were statistically significant ( t=- 2.91,-8.76, 3.59, P < 0.05). The levels of LDL-C, TG, TC in serum and liver of offspring male rats of 10 HI group were significantly lower than those of NI group ( t=3.28, 8.71, 3.44, 3.70, 3.49, 2.74, P < 0.05). The differences of mRNA expression levels of LDLR, ME, SREBP-1c in the liver of PN21 offspring male rats of 10 HI and NI groups were statistically significant ( t=- 3.50,-3.92, 5.58, P < 0.05). Among them, the levels of LDLR and ME in 10 HI group were higher than those in NI group, while the level of SREBP-1c in 10 HI group was lower than that in NI group. There no significant difference in CYP7A and TRβ mRNA levels between the two groups ( t=- 2.44, 3.20, P > 0.05). (2) Effects of 100 HI intake during pregnancy and lactation on PN120 offspring male rats: there were significant differences in serum FT 3, FT 4 and TSH levels of offspring male rats between 100 HI and NI groups ( t=- 4.39,-3.19, 4.72, P < 0.05). The levels of serum FT 3 and FT 4 in 100 HI group were lower than those in NI group, and the level of TSH in 100 HI group was higher than that in NI group ( P < 0.05). Compared with NI group, the serum and liver LDL-C, TG and TC levels in the offspring male rats of 100 HI group were significantly higher ( t=4.49, 12.85, 16.62, 4.35, 11.04, 16.01, P < 0.05). The differences of CYP7A, LDLR, ME, TRβ and SREBP-1c mRNA levels in liver of PN120 offspring male rats of 100 HI and NI groups were statistically significant ( t=26.40, 54.85,-10.98, 32.52, 10.50, P < 0.05). Among them, the CYP7A, LDLR, ME and TRβ mRNA levels in 100 HI group were lower than those of NI group, while the SREBP-1c mRNA level was higher than that of NI group ( P < 0.05). Conclusions:10 HI intake during pregnancy and lactation to the offspring male rats PN21 showed the serological changes of hyperthyroidism, the levels of blood lipids and liver lipids decreased, the levels of LDLR and ME mRNA increased, and SREBP-1c mRNA decreased in liver. However, 100 HI intake during pregnancy and lactation to the offspring male rats PN120 showed serological changes of hypothyroidism, the levels of blood lipids and liver lipids increased, the levels of CYP7A, LDLR, ME mRNA decreased, and SREBP-1c mRNA increased in liver.
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Objective To explore the correlation between apolipoprotein E (ApoE) gene polymorphism and urine Alzheimer-associated neuronal thread protein (AD7c-NTP) level in patients with Alzheimer's disease (AD) and mild cognitive impairment (MCI).Methods The cognitive function of 30 AD patients (AD group),30 MCI patients (MCI group) and 30 normal controls (NC group) was evaluated by neuropsychological batteries like MMSE,the Cambridge Cognitive Examination-Chinese Version (CAMCOG-C),etc.ELISA was used to test the urine level of AD7c-NTP.The genotypes of ApoE were analyzed by the high-resolution melting assay in blood samples.Results Compared with the NC group (0.59 (0.40,0.66) ng/ml),the urine level of AD7c-NTP in the AD group (1.03(0.80,1.41) ng/ml) and the MCI group (0.69(0.53,0.91) ng/ml) was increased (Z =33.727,P ＜0.01).The urine level of AD7c-NTP in the AD group was higher than that in the MCI group (Z =8.232,P ＜ 0.05).The level of AD7c-NTP in urine was negatively correlated with MMSE and CAMCOG-C scores (rMMSE =-0.604,P ＜ 0.01;rCAMCOG-C =-0.486,P ＜ 0.01).According to receiver operating characteristic curve,the optimal cutoff point of AD7c-NTP in urine for diagnosis of patients including AD and MCI was 0.70 ng/ml,with sensitivity of 71.7％ and specificity of 83.3％,and area under the curve of 0.82 (95％ CI 0.73-0.90,P ＜0.05).There were four genotypes comprising ε2/3,ε3/3,ε3/4 and ε4/4 for ApoE gene.The frequencies of ε4 carriers were 46.7％ (14/30),23.3％ (7/30) and 23.3％ (7/30) in the AD,MCI and NC groups,respectively.There was a notable increase in urine AD7c-NTP and a significant decrease in CAMCOG-C scores in MCI patients who harbored the ApoE ε4 allele (ZAD7c-NTP =4.857,P ＜ 0.05;ZCAMCOG-C =4.284,P ＜0.05).Conclusions The urine level of AD7c-NTP was significantly increased in AD and MCI patients,the higher the level of AD7c-NTP,the more serious the cognitive impairment.The ε4 carriers exhibited higher urine level of AD7c-NTP,but worse cognitive function compared to ε4 non-carriers in the MCI group.
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Objective To evaluate the efficacy of ancient classical prescriptions treating middle and advanced primary liver cancer.Methods Articles were searched from Pubmed, Embase, SCI, Cochrane Liarary and CNKI, VIP, WanFang Data, CBM databases. Randomized controlled trials about ancient classical prescriptions treating advanced primary liver cancer were collected. Results 17 studies were included, a total of 994 patients. The recent efficiency of ancient classical prescription combined with symptomatic therapy increased by 28% compared with single supportive and symptomatic therapy;the stable rate of life quality increased by 23%;the efficiency of TCM syndrome increased by 29%;the survival rates of 3 months, 6 months and 1 year increased by 16%, 36.7% and 58.5% respectively;the life quality score of later increased by 6.29 on average. Conclusion Ancient classical prescription combined with supportive and symptomatic therapy in advanced primary liver cancers is superior to single supportive and symptomatic therapy on recent efficiency, survival rate (3 months/6 months/1 year), quality of life and TCM syndrome. The conclusion of this study needs randomized controlled trials with larger samples, multicenter and high quality for further verification.
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Objective To investigate the effect of repetitive transcranial magnetic stimulation (rTMS) on the proliferation of neural stem cells in the subventricular zone (SVZ) and the expression of miR-9 in the ipsilesional hemisphere of rats with focal cerebral ischemia.Methods A rat model of acute focal cerebral ischemia was established using transient middle cerebral artery occlusion (tMCAO).Rats were then randomly assigned to a sham group,a control group or an rTMS group.Daily rTMS treatments (10 trains with 30 pulses per train and 50-second breaks between trains at 120％ of the resting motor threshold) were targeted at the ipsilesional MI cortex beginning one day after the tMCAO.After the treatment the proliferation of neural stem cells in the ipsilesional SVZ was identified by double immunofluorescence staining (BrdU/nestin).The expression of miR-9 was evaluated using quantitative PCR.Results Compared with the other two groups,BrdU + Nestin + cells in the ipsilesional SVZs of the rTMS group increased and the expression of miR-9 decreased significantly.Conclusion rTMS can promote the proliferation of neural stem cells and inhibit the expression of miR-9 in the ipsilesional hemisphere after focal cerebral ischemia.