Effect in sheep of dietary concentrate content on secretion of growth hormone, insulin and insulin-like growth factor-I after feeding

This study was designed to examine the effects of the proportion of concentrate in the diet on the secretion of growth hormone (GH), insulin and insulin‐like growth factor‐I (IGF‐I) secretion and the GH‐releasing hormone (GHRH)‐induced GH response in adult sheep fed once daily. Dietary treatments were roughage and concentrate at ratios of 100:0 (0% concentrate diet), 60:40 (40% concentrate diet), and 20:80 (80% concentrate diet) on a dry matter basis. Mean plasma concentrations of GH before daily feeding (10.00–14.00 hours) were 11.4 ± 0.4, 10.1 ± 0.5 and 7.5 ± 0.3 ng/mL on the 0, 40 and 80% concentrate diet treatments, respectively. A significant decrease in plasma GH concentration was observed after daily feeding of any of the dietary treatments and these decreased levels were maintained for 8 h (0%), 12 h (40%) and 12 h (80%), respectively (P < 0.05). Plasma IGF‐I concentrations were significantly decreased 8–12 h and 4–16 h after the end of feeding compared with the prefeeding level in the 40 and 80% concentrate diet treatments, respectively (P < 0.05). GHRH injection brought an abrupt increase in the plasma GH concentrations, reaching a peak 10 min after each injection, but, after the meal, the peak plasma GH values for animals fed 40% (P < 0.05) and 80% (P < 0.01) concentrate diet were lower than that for roughage fed animals. The concentrate content of a diet affects the anterior pituitary function of sheep resulting in reduced baseline concentrations of GH and prolonged GH reduction after feeding once daily.     

天然植物制剂“开口健”对小鼠淋巴细胞功能及营养生长因子的影响

目的：探讨口服＂开口健＂对小鼠淋巴细胞功能以及营养生长因子的影响。方法：36只ICR小鼠随机分为4组,即生理盐水组＂,开口健＂低、中、高剂量组。给小鼠连续灌胃10 d后,用MTT法检测淋巴细胞刺激指数,RT-PCR方法检测ConA刺激后淋巴细胞产生的IL-4、IL-10、IL-12和INF-γmRNA水平,ELISA方法检测小鼠血清胰岛素样生长因子（IGF-1）和生长激素释放肽（Ghrelin）水平。结果：口服＂开口健＂小鼠脾脏淋巴细胞SI显著高于对照组（P〈0.01）,并随＂开口健＂剂量的增加而升高;口服＂开口健＂小鼠脾脏淋巴细胞产生IL-4、IL-10、IL-12和IFN-γmRNA水平显著高于对照组（P〈0.05）。口服＂开口健＂显著提高了小鼠血清的IGF-1和Ghrelin水平（P〈0.05）,且与＂开口健＂剂量呈正相关性。结论：口服＂开口健＂可增强小鼠淋巴细胞功能并提高血清营养生长因子水平。     

Evaluation of the protective effect of lycopene on growth performance,intestinal morphology,and digestive enzyme activities of aflatoxinB1 challenged broilers

The current study was conducted to investigate the protective efficiency of dietary lycopene (LYC) supplementation on growth performance, intestinal morphology, and digestive enzyme activities aflatoxinB₁ (AFB₁) challenged broilers. A total of 240 days old Arber across male broiler chicks were randomly allocated in five treatments and six replicates (eight birds per replicate); feed and water were provided ad libitum during the 42 days experiment. The treatment diets were as follows: (i) Basal diet (control), (ii) Basal diet + 100 µg/kg AFB₁ contaminated diet, (iii) Basal diet + 100 µg/kg AFB₁ + 100 mg/kg LYC1, (iv) Basal diet + 100 µg/kg AFB₁ + 200 mg/kg LYC2, and (v) Basal diet + 100 µg/kg AFB₁ + 400 mg/kg LYC3. The results showed that the addition of LYC to AFB₁ contaminated broiler diets significantly increased (p < .05) average daily gain (ADG) and decreased feed conversion ratio (FCR) compared to the AFB₁ diet. AFB₁ diet decreased the intestinal villus height (VH) and crypt depth ratio (VCR) while increasing the crypt depth (CD). However, dietary LYC supplemented diets relieved the intestinal morphological alterations. Dietary LYC supplementation (200 and 400 mg/kg) significantly improved (p < .05) intestinal digestive enzyme amylase and lipase activities with AFB₁ contaminated diet. These findings suggested that LYC is a promising feed supplement in the broiler industry, alleviating the harmful effects of AFB₁.     

半胱胺对高邮鸭增重及相关激素分泌和基因表达的影响

随机选取 5日龄体况良好的雄性高邮鸭 2 4只 ,分成对照组和半胱胺 (CS)试验组。试验组每周按体重在日粮中添加 1次 CS(10 0 mg/ kg) ,以观察半胱胺对高邮鸭增重及相关激素分泌和基因表达的影响。结果表明 ,前 3周平均日增重试验组比对照组提高 12 .86 %,料肉比下降 12 .82 %;整个试验期平均日增重提高 4.5 3%,料肉比下降 4.0 3%。血清 IGF- 1水平 ,试验组为 (2 2 9.88± 8.6 9) μg/ L,显著高于对照组 (2 0 2 .31± 7.10 ) μg/ L(P<0 .0 5 ,n=10 ) ;血清 GH水平 ,试验组为 (0 .5 4± 0 .0 3) μg/ L,显著高于对照组 (0 .45± 0 .0 2 ) μg/ L(P<0 .0 5 ,n=10 ) ;垂体 GH m RNA的净灰度(net intensity) ,试验组为 (2 .2 3× 10 5± 0 .19× 10 5) ,显著高于对照组 (1.6 5× 10 5± 0 .12× 10 5) (P<0 .0 5 ,n=9) ,而下丘脑生长抑素 (SS) m RNA的净灰度 ,试验组为 (1.33× 10 5± 0 .10× 10 5) ,比对照组 (2 .14× 10 5± 0 .5 7× 10 5)降低37.85 %(P=0 .0 97,n=8) ,提示半胱胺对 SS基因转录水平可能没有影响。半胱胺促进生长和提高饲料转化率的机制 ,可能与 GH基因表达的上调和血清 IGF- 1水平的提高有关。     

干奶期不同能量水平对奶牛血中神经肽 Y和生长激素浓度的影响

将健康围产期奶牛30头随机分为3组．预产前28d按奶牛营养需要分别饲喂100％、120％、80％能量日粮，产后各组奶牛均饲喂标准的产奶日粮，至产后56d结束，观测干奶期不同能量摄入水平对围产期健康奶牛血中神经肽Y和生长激素浓度的影响。结果表明，干奶期低能量日粮饲喂，奶牛血中神经肽和生长激素浓度均高于其他2组，从产前14d至产后28d组间差异显著（P〈0.01；P〈0.05），提示低能量饲料饲喂干奶期奶牛，产后能量负平衡得到缓解。     

Significant effect of NSP‐ase enzyme supplementation in sunflower meal‐based diet on the growth and nutrient digestibility in broilers

The response of broiler chickens to 3 levels of sunflower meal and 2 levels of NSP‐ase enzyme combination (with and without) was investigated in 3 × 2 factorial arrangement under complete randomized design (CRD). A total of 240 Hubbard broiler chicks were fed on practical mash diets having 2950 kcal of ME and 21% CP from 1 to 42 days of age. The BW gain was not significantly reduced when 25% SFM was added in the diets during 1 to 42 days of age. Supplementation of NSP‐ase in broiler diets (day 1–42 overall) demonstrated non‐significant differences (p < 0.05) across the treatments in terms of FI and BWG. The difference in feed:gain at 15% or 20% SFM was observed to be non‐significant. Replacement of SBM with SFM or inclusion of SFM at higher level (25%) increased/deteriorated FCR. The addition of exogenous NSP‐ase showed a significant improvement (p < 0.01) in feed:gain. The improvement was clearly demonstrated when SFM was added to the experimental diet at 15% or even 20%. Supplementation of NSP‐ase at the 25% inclusion level could not, however, sustain the beneficial effect, which was possibly due to excessively high dietary CF. No difference was noted across the treatments regarding carcass response. Relative gizzard weight and intestinal weight were observed to be improved in birds consuming higher levels of SFM (p = 0.00). The digestibility of CF was observed to improve when SFM was used at 20% and 25% in the diets. No improvement in the digestibility of CF was observed with NSP‐ase supplementation, which meant other factors were clearly involved. Supplementation of NSP‐ase improved FCR up to 20% SFM. At 25% SFM, no improvement in the digestibility of CF was observed with NSP‐ase supplementation.     

In vitro growth of bovine oocytes in oocyte-cumulus cell complexes and the effect of follicle stimulating hormone on the growth of oocytes

Several successful in vitro culture experiments have used oocyte-cumulus cell-mural granulosa cell complexes (OCGCs) from early antral follicles (0.5–0.7 mm) for the growth of bovine oocytes. However, in studies related to in vitro oocyte maturation and in vitro embryo production, oocyte-cumulus cell complexes (OCCs) that have no mural granulosa cells have been widely used instead of OCGCs. The purpose of this study was to determine whether cumulus cells alone support oocyte growth. First, OCCs and OCGCs were cultured in vitro for 14 days to compare the integrity of the complexes as well as antrum formation. After 14 days, the diameter and meiotic competence of oocytes in OCCs and OCGCs were examined. Oocytes in OCCs grew fully and acquired meiotic competence similar to OCGCs, whereas antrum formation occurred later in OCCs as compared to OCGCs. Subsequently, the effects of follicle stimulating hormone (FSH) on in vitro growth of OCCs were examined for 14 days. When FSH was added to the culture medium, OCCs formed antrum-like structures one day earlier than those cultured without FSH. Oocytes cultured with 1 mIU/ml FSH grew fully and acquired meiotic competence. In contrast, when oocytes were cultured in media containing high concentrations of FSH, some of the OCCs collapsed and the number of degenerated oocytes increased. In conclusion, bovine oocytes in OCCs grow and acquire meiotic competence similar to OCGCs and, 1 mIU/ml FSH supports the development of OCCs and oocyte growth as observed in our culture system.     

NMDA对培养的大鼠腺垂体细胞分泌生长激素影响的研究

应用细胞培养、结合放射免疫测定法探讨了 N-甲基 -D-天冬氨酸 (NMDA)对培养的大鼠腺垂体细胞分泌生长激素 (GH)的影响。结果表明 :在腺垂体细胞培养中 ,试验组 (分别添加1 0 - 8、1 0 - 6 、1 0 - 4M NMDA)培养液中的 GH比对照组分别提高了 67.92 % ,87.46% ,1 0 0 .67% ,差异显著 (P <0 .0 5)。试验表明 NM-DA能直接刺激离体腺垂体细胞分泌 GH,并与NMDA呈剂量依赖关系     

Effects of oocyte-derived growth factors on the growth of porcine oocytes and oocyte–cumulus cell complexes in vitro

During oocyte growth and follicle development, oocytes closely communicate with cumulus cells. We examined the effects of oocyte-derived growth factors, growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15), on the growth and acquisition of meiotic competence of porcine oocytes collected from early antral follicles (1.2–1.5 mm). First, we confirmed that GDF9 and BMP15 mRNAs were expressed almost exclusively in the oocytes. Oocyte–cumulus cell complexes (OCCs) collected from early antral follicles were cultured in growth medium supplemented with 0–100 ng/ml of GDF9 or BMP15 for 5 days. GDF9 dose-dependently increased the OCC diameter, while BMP15 did not. GDF9 and BMP15 had no significant effects on oocyte growth (P > 0.05). When OCCs that had been cultured with 50 and 100 ng/ml BMP15 were subjected to a subsequent maturation culture, they expanded fully by gonadotropic stimulation and 49% and 61% of oocytes matured to metaphase II (MII), respectively. In contrast, GDF9 did not promote cumulus expansion, and < 10% of oocytes matured to MII. Based on the difference in cumulus expansion, we compared the expression of luteinizing hormone/choriogonadotropin receptor (LHCGR) and follicle stimulating hormone receptor (FSHR) mRNAs in cumulus cells. The level of LHCGR mRNA was increased in cumulus cells of the BMP15 group, although there were no significant differences in FSHR mRNA levels among the groups. These results suggest that GDF9 promotes the growth of OCCs and that BMP15 promotes LHCGR mRNA expression in cumulus cells during oocyte growth culture, which may contribute to cumulus expansion and oocyte maturation.