蜂王浆对日本大耳兔生长及繁殖性能的影响
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
本文结合日本大耳兔生物学特性,运用放射免疫法(RIA)、实时荧光定量PCR(real time-PCR)及同期发情等技术,研究了蜂王浆对日本大耳兔生长及繁殖性能的影响,旨在探索蜂王浆提高动物生长及繁殖性能的作用机制,进而为家畜生产性能的提高、生殖疾病的防治、以及濒临灭绝动物的保种等方面提供新的科学依据和重要借鉴。主要研究结果如下
     1.蜂王浆对雄性日本大耳兔生长及繁殖性能的影响:分别按体重0.2%(高剂量组)和0.1%(低剂量组)的量,给高、低剂量组的18只2月龄雄性日本大耳兔每天空腹灌胃新鲜蜂王浆,对照组18只雄兔灌胃体重0.1%的生理盐水,每周同一时间称重。运用RIA依次测定灌胃Od、40d、60d和80d的血清性激素六项:促黄体素(LH),促卵泡素(FSH),雌二醇(E2),孕激素(P),睾酮(T)和催乳素(PRL);70d后活体检测精子密度、活力和畸形率;80d后屠宰并分离主要脏器,计算各自脏器系数;右侧睾丸作成石蜡切片用于组织形态学观察。结果表明:(1)灌胃之前,3个实验组之间的血清性激素六项均差异不显著(P>0.05)。灌胃40d、60d和80d后,高、低剂量组的LH.FSH和T均极显著高于对照组(P<0.01),高、低剂量组之间差异不显著(P>0.05);而E2、P和PRL在3组之间均差异不显著(P>0.05)。(2)高、低剂量组的精子密度极显著大于对照组(P<0.01),高、低剂量组之间差异不显著(P>0.05);低剂量组的精子活力极显著高于对照组,而对照组又极显著高于高剂量组(P<0.01);3组之间的精子畸形率差异不显著(P>0.05)。(3)第0-8周,3组之间的每周龄体重差异不显著(P>0.05);之后,高、低剂量组极显著高于对照组(P<0.01),高、低剂量组之间差异不显著(P>0.05)。屠宰测定时,高、低剂量组的雄兔睾丸、下丘脑和脾脏脏器系数都极显著大于对照组(P<0.01),高、低剂量组之间无显著差异(P>0.05);脑、肺和膀胱等其它主要脏器系数均差异不显著(P>0.05)。(4)灌胃80d后,对照组雄兔睾丸曲细精管生精上皮细胞数量明显少于试验组,生精上皮较薄,生精上皮细胞排列疏松,中央管腔更大管腔内大多为初级精母细胞和次级精母细胞;试验组的曲细精管管腔相对缩小,被精子细胞及精子所充实,细胞层数增多,精原细胞附于基膜,初级精母细胞、精子细胞和精子依次紧密排列延伸至管腔内,核染色明显管腔中可见大量的精子。本研究结果说明:蜂王浆能促进雄兔下丘脑、睾丸和脾脏发育;灌胃体重0.1%的蜂王浆能显著提高精子密度和精子活力;蜂王浆灌胃40d后,能显著提高血清中的LH、FSH和T浓度,对E2、P和PRL没有影响。
     2.蜂王浆对初情期前雌性日本大耳兔生长发育和性激素受体mRNA表达的影响:分别按体重0.2%和0.1%的量,给高、低剂量组12只50日龄的雌性日本大耳兔每天进行空腹灌胃新鲜蜂王浆,对照组12只雌兔灌胃体重0.1%的生理盐水。40d后股动脉放血处死,摘取下丘脑、右侧卵巢和右侧子宫,用于激素受体mRNA表达的检测;摘取心脏、左侧子宫和左侧卵巢等器官,用于脏器系数的测定;采用RIA法测定血清性激素六项。结果表明:(1)灌胃12d,对照组兔子没有换毛现象,高、低剂量组兔子分别出现67%和75%的换毛率。(2)蜂王浆对体重、心脏和卵巢等脏器系数无显著影响(P>0.05)。(3)高、低剂量组血液中的E2浓度极显著高于对照组(P<0.01),高、低剂量组之间差异不显著(P>0.05);其它性激素在3个实验组之间差异不显著(P>0.05)。(4)高剂量组下丘脑GnRH的mRNA表达量极显著低于对照组和低剂量组(P<0.01),低剂量组与对照组之间差异不显著(P>0.05);高剂量组卵巢LHR和FSHR的mRNA表达量极显著低于对照组(P<0.01),显著低于低剂量组(P<0.05),低剂量组与对照组之间差异不显著(P>0.05);高剂量组子宫ERα和卵巢ERβ的mRNA表达量极显著低于对照组(P<0.01),但高、低剂量组之间以及低剂量组与对照组之间均差异不显著(P>0.05)。本研究结果说明:蜂王浆可以促进初情期前雌性日本大耳兔换毛,提高血清中E2水平,抑制下丘脑GnRH、卵巢LHRFSHR、ERβ以及子宫ER。的nRNA表达,对主要脏器系数无显著影响。
     3.蜂王浆对成年雌性日本大耳兔繁殖性能的影响:首先研究氯前列腺烯醇钠(PG)诱导健康经产母兔同期发情的效果,然后分别按体重0.2%和0.1%的量,给PG处理后的高、低剂量组健康经产母兔每天空腹灌胃新鲜蜂王浆,对照组灌胃体重0.1%的生理盐水,18 d后配种,计算繁殖性能相关指标。结果显示:(1)注射0.25mg/只PG后的健康经产母兔,LH、FSH和E2浓度分别在9h和48h达到最大值和最小值,P浓度则为最小值和最大值;PG处理后每天的LH、FSH、E2均在19:00达最大值,P达最小值:PG处理后第12d的LH、FSH和E2均高于第4d、8d和16d,P则低于第4d、8d和16d,差异达显著水平(P<0.05)。(2)蜂王浆灌胃高、低剂量组的FSH、LH、E2和P浓度均比对照组提前达到最高值和最低值高、低剂量组之间差异不显著(P>0.05),最高值与最低值分别在3个实验组之间差异不显著(P>0.05)。(3)高、低剂量组的窝产仔数和成活率与对照组之间差异不显著(P>0.05);卵泡数、排卵数和初生个体重、初生窝重泌乳力、断奶个体重、断奶窝重都极显著高于对照组(P<0.01),高、低剂量组之间均差异不显著(P>0.05)。这些结果表明:注射0.25mg/只的PG能使母兔分别在9h和48h达到发情盛期和发情后期,12d后进入下一个发情周期,每天的激素极值出现在19:00。蜂王浆能缩短母兔发情周期,对处于相同生理周期母兔的激素没有影响;蜂王浆能促进母兔卵泡发育和排卵,提高初生窝重、初生个体重、泌乳力、断奶个体重和断奶窝重,对母兔窝产仔数没有影响。
A series of techniques including radioimmunoassay (RIA), real-time fluorescence quantitative PCR and estrous synchronization were used in conjunction with the biological characteristics of Japanese white rabbit to detect the effects of Royal Jelly (RJ) on the growth and reproductive performance in Japanese white rabbits, with the aim to give hints for the improvement of animal husbandry production the prevention and therapy of reproductive disease, and the protection of endangered animal species.
     1. Effects of royal jelly on growth and reproduction performance of male Japanese white rabbits:Fifty four two-month-old male Japanese white rabbits were randomly and equally divided into three treatment groups which received RJ or saline by intragastric administration once a day for 80 days. The high and low dose groups received RJ of 0.2% and 0.1% of body weight, respectively, while the control group was administered with 0.1% body weight of saline. The rabbits were weighted once a week and slaughtered after 80 days. Levels of circulating FSH, LH, E2, P, T and PRL in plasma were determined by RIA on days 0,40,60 and 80 of treatment. Sperm density, vitality and abnormality rate were determined by biopsy prior to slaughter. After slaughter, organs were separated and each organ coefficient was calculated. The right testis was embedded in paraffin for histological examination. The results were as follows.
     (1) Of the six tested reproductive hormones, no difference was detected among the three groups before treatment. On days 40,60 and 80 of treatment with RJ, the levels of FSH, T and LH in the control group were significantly lower than those in the high or low dose groups (P<0.01). No significant difference was found for P, E2 and PRL levels. All of the six reproductive hormones had no difference between high and low dose groups.
     (2) The density of sperm was significantly higher in the high dose and low dose treatment groups than in the control group (P<0.01), but there was no significant difference between high and low dose groups. With regard to sperm motility, the low dose group was significantly greater than the control group while the high dose group was significantly lower than the control group (P<0.01). There was no significant difference in the frequency of abnormal sperm among the three groups.
     (3) Prior to 8 weeks, body weight among the three groups did not differ significantly. Beginning on day 56, the body weights were significantly higher in the high and low dose groups than in the control group (P<0.01), but high and low dose groups were not significantly different from each other. After slaughter, the organ coefficients of the male rabbit testis, hypothalamus and spleen in the high and low dose group were significantly higher than in the control group (P<0.01), while the organ coefficients of brain, lung and bladder were not significantly different among the three groups. The organ coefficients were not significantly different between the high and low dose groups.
     (4) Following 80 days of RJ administration, the cell number of the testicular seminiferous tubule epithelium was significantly higher in both treated groups than in the control group. Compared to the histology of the testes in the control group, the following changes were observed in the RJ-treated groups:Characters of the testicular seminiferous tubule appeared to be thin seminiferous epithelium; seminiferous epithelium cells were loosely arranged with larger central lumen; most cells in the lumen were the primary spermatocytes and secondary spermatocytes in the control group; however the seminiferous tube cavity was relatively narrow and was enriched by the sperm cells and sperm. Cell layers were increased. spermatogonia attached base membrane. Primary spermatocytes, spermatids and sperm were packed closely and extended to the lumen, clear nuclear staining. A large number of sperms were observed in the lumen in the RJ given groups.
     Taken together, these results suggest that RJ can promote the development of hypothalamus, spleen and testis of male rabbits; sperm density and sperm motility were significantly increased in the low dose group, and serum levels of FSH, T and LH (but not of P, E2 and PRL) were significantly increased after 40 d of RJ administration.
     2. Effects of royal jelly on growth, development and expression of sex hormone receptor mRNA in prepubertal female Japanese white rabbits:Twelve 50-days-old fasting female rabbits were given fresh RJ (0.2% or 0.1% of body weight) or saline (0.1% of body weight) once a day for 40 days. Then the rabbits were sacrificed by femoral artery bleeding and the hypothalamus, the right side of ovary and the uterus were quickly dissected for RT-PCR analysis of hormone receptor mRNA expression. In addition the organs like heart, the left side of the uterus and ovaries were collected for organ coefficient analysis. The serum levels of FSH, LH, E2, P, T and PRL were determined by RIA. The results were as follows.
     (1) Moulting was observed after 12 d in 67% and 75% of rabbits treated with high and low doses of RJ, respectively, but was not observed in the control group.
     (2) Royal Jelly had no effect on body weight or the organ coefficients of heart, hypothalamus and ovaries.
     (3) The levels of serum E2 in high and low dose groups were significantly higher than that in the control group. No significant difference was found in other sex hormones.
     (4) Uterine ERαand ovary ERp mRNA levels were lower in high and low dose groups than in the control group. There was a significant difference between the high dose and control groups in the level (P<0.01). High and low dose groups, low dose and control group were not significantly different. Hypothalamic GnRH mRNA was lower in the high dose treatment group compared with the control and low dose groups (P<0.01). LHR and FSHR mRNA levels were significantly decreased in the high dose group (P<0.01) and low dose group (P<0.05) relative to the corresponding levels in the control group.
     Taken together, these results suggest that RJ can increase serum E2 levels in prepubertal female Japanese white rabbits, while suppress the mRNA expression of GnRH in hypothalamus, ERαin the uterus, and ERp, FSHR and LHR in ovary.
     3. Effects of royal jelly on reproductive performance of mature female Japanese white rabbits:The effect of PG on the homochronous of healthy and multiparous female rabbits was studied at first. After that, the rabbits were injected with PG (0.25mg per rabbit) and divided into three RJ treatment groups as described above. They were then mated after a complete estrous to investigate the effect of RJ on the reproductive performance. The results were as follows.
     (1) Injection of 0.25mg PG per rabbit caused the levels of LH, FSH and E2 reaching peak and trough at 9h and 48h, respectively; P came into trough and peaked at 9h and 48h, respectively. After PG treatment, the levels of LH, FSH and E2 reached peak at 19:00 each day, and P came into trough; the levels of LH, FSH and E2 on day 12 after PG treatment was higher than those on days 4,8 and 16, P was lower(P<0.05).
     (2) The peak of LH, FSH, E2 and the trough of P appeared earlier in RJ treatment groups than the control group, no difference was observed between high and low dose RJ teatement groups, neither peak nor trough was different among the three groups.
     (3) There was no significant effect of RJ on litter size and survival rate. However, the number of ovulation and follicle, individual birth weight, litter weight at birth, lactation ability, litter weight and individual weight at weaning were significantly lower in the control group compared with the high and low dose groups (P<0.01), and high and low dose groups were not significantly different.
     Taken together, these results suggest that the injection of 0.25mg PG per rabbit can make the female rabbits reach estrus peak at 9h and come into dioestrus at 48h after treatment; it started into the next estrous cycle at 12d; peak and trough of sex hormone mainly appeared at 19:00 each day. RJ can shorten the estrous cycle of female rabbits, but has no significant effect on hormone levels in the same estrous cycle. RJ can promote the development of follicular and ovulating, improve the litter weight at birth, individual birth weight, lactation ability, litter weight and individual weight at weaning, but has no effect on litter size.
引文
1.陈盛禄主编.中国蜜蜂学.北京:中国农业出版社,2001.
    2. Kimura Y, Nagai H, Miyamoto M, et al. Identification of a royal jelly glycoprotein that carries unique complex-type N-glycans harboring the T-antigen (Galβ1-3GalNAc) unit. Biosci Biotechnol Biochem,2010,74(10):2148-2150.
    3. Cherniak EP, Bugs as drugs, Part 1:insects:the new alternative medicine for the 21st century? Altern Med Rev,2010,15(2):124-135.
    4. Elnagar SA.Royal jelly counteracts bucks summer infertility. Anim Reprod Sci,2010,121(1-2): 174-80.
    5. Yang XY, Yang DS, Wei-Zhang, et al.10-Hydroxy-2-decenoic acid from Royal jelly:a potential medicine for RA. J Ethnopharmacol,2010,128(2):314-321.
    6. Malecova B, Ramser J, O'Brien JK, et al. Honeybee (Apis mellifera L.) mrjp gene family: computational analysis of putative promoters and genomic structure of mrjp 1, the gene coding for the most abundant protein of larval food. Gene,2003,303:165-75.
    7. Albert S, Klaudiny J. The MRJP/YELLOW protein family of Apis mellifera:identification of new members in the EST library. J Insect Physiol,2004,50(1):51-9.
    8.曾志将主编.养蜂学.北京:中国农业出版社,2003.
    9.茹清静.蜂王浆活性成分与护肝机理研究.中西医结合肝病杂志.2002,12(6):36-37.
    10. Palma MS. Composition of freshly harvested Brazilian royal jelly identification of carbohydrates from the sugar fraction. Journal of Apicultural Research,1992,31:42-44.
    11. Hanes J, Smiuth J. Identification and Partial characterization of the major royal jelly protein of the honeybee(Apis Mellifera L.). Journal of Apicultural Research,1992,31:22-26.
    12. Tamura T. Royal jelly from the standpoint of clinical pharmacology. Honeybee Science,1985,6(1): 117-124.
    13. Schmitzova J, Albert S, Schroder W, et al. A family of major royal jelly proteins of the honeybee Apis mellifera L. Cell Molecular Life Science,1998,54(9):1020-1030.
    14. Fujii A. Pharmacological effect of royal jelly. Honeybee Science,1995,16(1):97-104.
    15. Takenaka T, Yatsunami K, Echigo T. Changes in quality of royal jelly during storage. Nippon Shokuhin Kogyo Gakkaishi,1986,33(1):1-7.
    16. Takenaka T. Nitrogen components and carboxylic acids of royal jelly. In chemistry and Biology of Social Insects (edited by Eder J, Rembold H), Munich, German Federal Republic, Verlag J. Papemy,1987,162-163.
    17. Emanuele B, Maria F, Anna G, et al. Determination and changes of free amino acids in royal jelly during storage. Apidologie,2003,34:129-137.
    18. Lercker G, Capella P, Conte LS, et al. Components of Royal Jelly II. The lipid fraction, hydrocarbons and sterols. Journal of Apicultural Research,1982,21:178-184.
    19. Giulio S. Determination of sugars in royal jelly by HPLC. Apidologie,2006,37:84-90.
    20. Lercker G, Capella P, Conte LS, et al. Components of Royal Jelly I:Identification of the organic acids Lipids. Journal of Apicultural Research,1981,16:912-919.
    21. Mishref A, Afify AS. Effect of feeding amino acids to honeybees on the chemical composition of royal jelly. Proceedings of the Fourth International Conference on Apiclture in tropical Climates, Cairo, Egypt,6-10 November 1988,74-79.
    22.方国祯,方建生,田树革.蜂王浆成份及其分析方法研究进展.中国乳品工业,12(6):280-282.
    23. Schmidt JO, Buchmann SL. Other products of the hive, In:The hive and the honeybee. JM Graham, ed. Dadant& Sons, Hamilton, Illinois, USA.1992,927-988.
    24. Barker SA, Foster AB, Lamb DC. Identification of 10-hydroxy-2decenoic acid in royal jelly. Nature, 1959,183:996-997.
    25.张复兴主编.现代养蜂生产.北京:中国农业大学出版社,1998,446-455.
    26. Vecchi MA, Sabatini AG, Grazia L, et al. Ⅱ contenuto in vitamine come possibile elemento di caratterizzazione della gelatina reale. Apicoltura,1988,4:139-146.
    27. Kreze A, Toman A. Effect of royal jelly on the exertion of corticoids. Vnitr Lek.1969,15(14): 341-346.
    28. Satoshi M, Kazu MS, Yoichiro I, et al. Royal jelly has estrogenic effects in vitro and in vivo. Journal of Ethnopharmacology,2005,101:215-220.
    29.赵国华.蜂王浆保健功能解析.蜜蜂杂志,1999,(4):18-19.
    30. Wang GY, Lin ZB. Effects of 10-hydroxyl-2-decenoie acid on phagocytosis and cyktokines production of peritoneal macrophages in vitro. Acta pharmacologica sinica,1997,18(2):180-182.
    31. Tamura T, Fujii A, Kuboyama N, Effect of royal jelly on experimental transplantable tumors. Proceedings of the International Congress of Apiculture, Nagoya, Japan,1985,474-477.
    32. Tamura T, Fujii A, Kuboyama N. Antitumor effects of royal jelly RJ. Journal of Japanese Pharmacology,1987,89:73-80.
    33. Emori Y, Oka H, Ohya O, et al. The protective effect of royal jelly against the hemopoiesis dysfunction in X-irradiated mice. Biotherapy (JPn),1998,12:313-319.
    34. Emori Y, Oka H, Ohya O, et al. The Protective effete of royal jelly on cecal ligation and puncture-induced sepsis in X-irradiated mice. Biotherapy (JPn),1998,12:1143-1148.
    35.张敬,戴秋萍,刘艺敏等.RJ冻干粉对小鼠肿瘤的抑制作用.同济大学学报医学版,2001,22(5):13-14.
    36. Oka H, Emori Y, Kobayashi N. Suppression of allergic reaetions by royal jelly in association with the restoration of macrophage function and the improvement of Th1 and Th2 cell responses. International immunopharmacology,2001,1:521-532.
    37. Iwao O, Yoshifumi T. Major royal jelly protein 3 modulates immune responses in vitro and in vivo. Life Sciences,2003,73:2029-2045.
    38. Okuda H, Kenji K, Morimoto C, et al. Studies on insulirr like substances and inhibitory substances toward angiotensirr converting enzyme in royal jelly. Honeybee Science,1998,19(1):9-14.
    39. Matsui T, Yukiyoshi A, Doi S, et al. Gastrointestinal enzyme production of bioactive peptides from royal jelly protein and their antihypertensive ability in SHR. The journal of nutritional biochemistry,2002,13(2):80-86.
    40. Katsu T, Chie Y. Effect of free radical scavenging system in mice bearing ehrlich ascites carcinoma. Biological pharmacology bulletin,2004,27:189-192.
    41. Uno K, Kondo A. A study of clinical significance of leukocyte migration inhibition test in drug-induced hypersensitivity pneumonitis. Arerugi,1995,44(12):1401-1409.
    42. Vittek J. Effect for royal jelly on serum lipids in experimental animals and human with atherosclerosis. Experientia,1995,51:927-935.
    43.沈新南,陆瑞芳,何更生等.RJ冻干粉对实验性高脂血症及血栓形成的影响.中华预防医学杂 志,1995,29(1):27-29.
    44. Kitaharaa T, Satoa N, Ohyaa Y, et al. The inhibitory effec of hydroxy acids in royal jelly extract on sebaceous gland lipogenesis. Journal of dermatological science,1995,10:75-84.
    45. Fujiwara S, Imai J. Yaeshima T, et al. A potent antibacterial protein in royal jelly. Purification and determination of the primary structure of royalisin. Journal of biology chemistry,1990,265(19): 11333-11337.
    46.肖静伟、王戎疆,李绍文等.RJ中一种有抗菌活性的小肽.昆虫学报,1996,39(2):133-140.
    47. Bilikova K, Gusui W, Jozef S. Isolation of a peptide fraction from honeybee royal jelly as a potential antifoulbrood factor. Apidologie,2001,32:275-283.
    48. Husein MQ, Kridli RT, Humphrey WD. Effect of royal jelly on estrus synchronization and pregnancy rate of wews using fluorogestone acetate sponges. Journal of experimental animal science,1999, supplement 1.
    49.倪辉,陈申如.微量活性成分是蜂王浆的主要保健成分.养蜂科技,2001,(1):7-9.
    50. Karl JK, Cynthia NC. Inorganic phosphate assay with malachite green:an improvement and evaluation. Journal of Biochemistry biophys methods,1982,7:7-13.
    51. Husein MQ, Kridli RT. Reproductive responses following royal jelly treatment administered orally or intramuscularly into progesterone-treated Awassi ewes. Animal Reproduction Science,2002, 74:45-53.
    52. Husein MQ, Haddad SG. A new approach to enhance reproductive performance in sheep using royal jelly in comparison with equine chorionic gonadotropin. Animal Reproduction Science,2006,93: 24-33.
    53. Kridli RT, Husein MQ, Humphrey WD. Effect of royal jelly and GnRH on the estrus synchronization and pregnancy rate in ewes using intravaginal sponges. Small Ruminant Research, 2003,49:25-30.
    54. Kridli RT. Al-Khetib SS. Reproductive responses in ewes treated with eCG or increasing doses of royal jelly. Animal Reproduction Science,2006,92:75-85.
    55.胥保华.蜂王浆对动物机体生理机能的调节作用.山东畜牧兽医,1999(1):34.
    56. Ahmed TA. Jehan A, Muhamad. Midcycle pericoital intravaginal bee honey and royal jelly for male factor infertility. International Journal of Gynecolbgy and Obstetrics,2008,101:146-149.
    57.蔡柳,林亲录.蜂王浆的研究进展.中国食物与营养,2007(8):19-22.
    58.金汤东,陈巨洪,赵健等.蜂王浆不同添加量对种鸡产蛋率影响试验.养蜂科技,1999(6):29-30.
    59.许德民.蜂王浆对喂养名贵金丝雀的作用.中国养蜂,2002,53(4):14.
    60.陈华生,高育仁,黄文忠等.蜂王浆对提高白鹇繁殖能力的试验初报.蜜蜂杂志,1997(8):8-9.
    61.孙亮先,林春玉,陈朝阳等.饲喂蜂王浆对果蝇繁殖力影响的研究.中国蜂业,2008,59(3):5-6.
    62.王立新,杜娟,张树杰等.饲喂胡萝卜和蜂王浆对黄粉虫繁殖力的影响.昆虫知识,2005,42(4):434-438.
    63.王克健.家兔品种基础知识.甘肃农业,2002,(2):29-34.
    64.徐汉涛.家兔的品种介绍.农村养殖技术,2007,(6):4-7.
    65.魏泓.医学实验动物学.成都:四川科学技术出版社,2001.
    66.杨正.现代养兔.北京:中国农业出版社,2001.
    67.黄良虎.家兔繁殖障碍的原因及防治措施.中国养兔杂志,1997,(4):8-9.
    68.张家口.养兔学.北京:农业出版社,1981.
    69.李长生,王喜萍,王丽梅.家兔的繁殖生理特性.畜牧兽医杂志,2001,20(4):22-23.
    70. Rabbits, chapter in Assistant Laboratory Animal Technician. Training Manual, American Association for Laboratory. Animal Science, Memphis, TN,2008.
    71.陈主初,吴端生.实验动物学.长沙:湖南科学技术出版社.2001.
    72.于守德.獭兔最佳配种时机和乏情母兔的配种方法.中国养兔杂志,1998,(4).
    73.前岛一淑.新实验动物学.朝仓书店.1986.
    74.王凌燕,王树迎,侯衍猛,谭雷涛.哺乳动物下丘脑-垂体-卵巢轴的研究进展.动物医学进展,2005,26(7):8-11.
    75. Granum PEJ. Food Microbiology. Copenhagen:Elsevier Science.1990.
    76. Lysiak JJ, Nguyen QA, Tuner TF. Fluctuations in rat testicular interstitial oxygen tensions alelinked to testicular vasomotion:persistence after repair of torsion. Biol Reprod,2000,63(5):1383-1389.
    77. Haagsma J. Pathogenetic anaerobic bacteria and the environment. Rew Sci Tech Off lnt Epiz,1991, 10(3):749-764.
    78. Donnez PJ, Dolmans MM. Demylle D, et al. Livebirth after arthotopic transplantation of cryopreserved ovarian tissue. Lancet,2004,364 (9443):1405-10.
    79. Gook DA, Mccully BA, Edgar DH, et al. Development of antral follicles in human cryopreserved ovarian tissue fol lowing xenografting. Hum Reprod,2001,16 (3):417-422.
    80.施新猷.医用实验动物学.西安:陕西科学技术出版社.1989.
    81. Holmes.D. An introduction to clinical Laboratory animal medicine,1984.
    82.张明,朱庆,郑鸿培.家畜卵泡抑制素研究进展.黑龙江畜牧兽医,2005,(11):83-85.
    83.唐胜球,董小英,邹晓庭.家畜卵泡抑制素的研究进展.中国畜牧杂志.2003,39(5):54-56.
    84. JohnGP. Glycoprotein homones:structure and function. Ann. Rev. Biochem,1981, (50):465-495.
    85. Jean Closset, Georges Hennen. Porcine Follitropin. Eur. J. Biochem,1978,86:105-113.
    86.任春明,字向东,张重庆等.卵泡刺激素(FSH)的研究进展.畜禽业,2006,(20):10-13.
    87.张家骅.家畜生殖内分泌学.北京:中国文化教育出版社,2004.
    88.师莉莉,薛晓鸥,姜恩魁.雌激素受体与女性生殖轴关系的研究进展,2004,9.
    89. Ben-Jonathan N, Liby K, Mcfarland M, et al. Prolactin as an Autocrine/paracrine growth factor in human cancer. Trends Endocrinal Metab,2002,13(6):245-250.
    90. Dawson A, Sharp PJ. The role of proclactin in the development of reproductive photorefractorriness and postnuptial molt in the European starling (Stunus vulgaris). Endocrinologe,1998,139: 485-490.
    91.杨传任.家畜生殖激素.北京:中国农业出版社,1995.
    92.王强,侯正录.GnRH的研究进展.生物学杂志,2003,20(5):40-41.
    93. Huang WQ, Yao B, Sun L, et al. Lmmunohistochemical and insitu hybridization studies of GnRH and its receptor. Life Science,2001,68(15):1727-1731.
    94. Braun T, Schofield PR, Sprengel R. Amino-terminal leucine -rich repeats in gonadotropin receptors determines hormone selectivity. Embo,1991,10(7):1885-1890.
    95. Parmentier M, Libert F, Maenhaut C, et al. Molecular cloning of the thyrot ropin receptor. Science, 1989,246:1620-1622.
    96. Sprengel R, Braun T, Nikolics K, et al. The testicular receptor for follicle stimulating hormone: structure and functional expression of cloned cDNA. Mol Endocrinol,1990,4 (4):525-530.
    97.陈雪雁,陈克铨,陈实平.FSH受体的特异性和表达的调控.解剖学报,1999,30(3):284-287.
    98. Meduiri G, Charnaux N, Driancourt MA, et al. Messenger RNA expression for the follicle stimulating hormone in oocytes. Jclin Endocrinol Metab,2002,87(5):2266-2276.
    99. Patsoula E, Loutradis D, Drakakis P, et al. Messenger RNA expression for the follicle stimulating hormone receptor and luteinizing hormone receptor in human oocytes and preimplanting preimplantingstage embryos. Fertil Steril,2003,79(5):1187-1193.
    100. Oxberry BA, Greenwald GS. An autoradiographic study of the binding of I-labeled follicle-stimulating hormone, human chorionic gonadotropin and prolactin to the hamster ovary throughout the estrous cycle. Biol Reprod,1982,27:505-516.
    101. Charlton HM, Parry D, Halpin DMG, Webb R. Distribution of I-Iabeled follicle-stimulating hormone and human chorionic gonadotropin in the gonads of hypogonadal (hpg) mice. Endocrinol,1982,93:247-252.
    102. Shima K, Kitayama S, Nakano R. Gonadotropin binding site in human ovarian follicles and corpora lutes during the menstrual cycle. Pbstet Gynecol,1987,69:800-806.
    103. Cynthia K. Sites. Follicle-stimulating hormone (FSH) increase FSH receptor messenger ribonucleic acid while decreasing FSH binding in cultured porcine granulose cells. Endocrinology, 1994,1:411-417.
    104. Menon KM, Munshiu M, Clouser CI, et al. Regulation of luteinizing hormone human chorionic gonadotropin receptor expression perspective. Biol Reprod,2004,70(4):681-866.
    105.吴馨培,王树迎.莱芜黑山羊卵巢FSHR、LHR的免疫组化定位研究.生命科学研究,2006,4(10):367-371.
    106. Derecka K, Pietila EM, Rajaniemi H J, et al. Cycle-dependent LH/hCG receptor gene expression in porcine nongonadal reproductive tissues. J Physiol Pharmacol,1995,46:4677-4685.
    107. Shemesh M, Mizrachi D, Gurevich M, et al. Expression of functional luteinizing hormone (LH) receptor and its messenger ribonucleic acid in bovine endometrium:LH augmentation of cAMP and inositol phosphate in vitro and human chorionic gonadotropin (hCG) augmentation of peripheral prostaglandin in vivo. Reprod Biol,2001 (1):13-32.
    108. Stepien A, Derecka K, Gawronska B, et al. LH/hCG receptors in the porcine uterus-a new evidence of their presence in the cervix and myometrium. J Physiol Pharmacol.2000.51:917-931.
    109. Shemesh M. Mizrachi D, Gurevich M, et al. Functional importance of bovine myometrial and vascular L H receptors and cervical FSH receptors. Semin Reprod Med,2001,19:87-96.
    110. Kessel B, Liu YX, Jia XC, et al. Autocrine role of estrogens in the augmentation of luteinizing hormone receptor formation on cultured rat granulose cells. Biology of Reproduction,1985,32: 1038-1050.
    111. Liu Y X, Hsueh AJW. Autocrine role of endogenously produced estrogen in the enhangcement of aromatase activity, progesterone production and LH receptor in cultured rat granulose cells. Chinese Journal of Physical Science,1986,1:1-9.
    112. Roy SK. Epidermal growth factor and transforming growth factor-β modulation of follicle-stimulating hormone induced deoxyribonucleic acid synthesis in hamster preantral and early antral follicles. Biology of Reprduction,1993,48:552-557.
    113. Findlay JK, An update on the rates of inhibin, activin and follistatin as local regulators of folliculologenesis. Biology of Reproduction,1993,48:15-23.
    114. Green S, Walter P, Kumar V, et al. Human oestrogen receptor cDNA:sequence, expression and homology to verb-A. Nature,2003,20(13):134-139.
    115.范颖,沙立春,李斌.雌激素受体亚型与雌激素依赖性妇科疾病的关系.中国妇幼保健,2007,22:970-972.
    116. Kuiper GG, Enmark E, Peho-Huikko M, et al. Cloning of a novel receptor expressed in rat prostate and ovary. Proc Natl Acad.Sci USA,1996,93(12):5925-5930.
    117. Bord S, Homer A, Beavan S, et al. Estrogen receptors alpha and beta are differentially expressed in developing human lone. J Clin Endocrinol Metab,2001,86(5):2309-2341.
    118. Muramatsu M, Inoue S. Estrogen receptors:How do they control repro-ductive and nonreproductive functions? Biochem Biophys Res Commun,2000,270(1):1-10.
    119. Ogawa S, Homi T, Shiraki M, et al. Association of estrogen receptor beta gene polymorphism with bone mineral density. Biochem Biophys Res Common,2000,269(2):527-541.
    120. Zhou S, Zilberman Y, Wassermmm K, et al. Estrogen modulates estrogen receptor alpha and beta expression, osteogenic activity, and apoptosis in mesenchymal stem cells (MSCs) of osteoporotic mice. Cell Biochem,2007,81(S36):144-155.
    121. Anwar A, McTeman PG, Anderson LA, et al. Site-specific regulation of oestrogen Receptor-alpha and-beta by oestradiol in human adipose tissue. Diabetes Obes Metab,2001,3(5):338-349.
    122. Z WH, Saji S, Makinen S, et al. Estrogen receptor(ER) beta, a modulator of ERalpha in the ute-us. Proc Natl Acad Sci USA,2006,97(11):5936-5941.
    123. Ren MQ, Kuhn G, Wegner J, et al. Feeding daidzein to late pregnant SOWS influences the estrogen receptor beta and type 1 insulin like growth factor receptor mRNA expression in newborn piglets. Endocrinol,2007,170(1):129-135.
    124. Tena-Sempere M, Gonzalez LC, Pinilla L, et al. Neonatal imprinting and regulation of estrogen receptor alpha and beta mRNA expression by estrogen in the pituitary and hypothalareas of the male rat. Neuro endocrinology,2001,73(1):12-25.
    125. O'Brien ML, Park K In Y, Park-Sarge OK. Characterization of estrogen receptor beta (ERbeta) messenger ribonucleic acid and protein expression in rat granulosa cells. Endocrinology,1999, 140(10):4530-4541.
    126. Chiang CH, Cheng KW, Igarashi S, et al. Hormonal regulation of estrogen receptor alpha and beta gene expression in human granulose-uteal cells in vitro. Clin Endocrinol Metab,2006,85(10): 3828-3839.
    127. Guo C, Savage L, Sarse KD, et al. Gonadotropins decrease estrogen receptor-beta messenger ribonucleic acid stability in rat granulos cells. Endocrinology,2005,142(6):2230-2237.
    128.陆耀祖,刘学锋.现代畜牧兽医,2007,11:18-19.
    129.曾星凯,谢国秀,吴小波等.蜂王浆活性组分癸烯酸和氨基酸含量变化及对小白鼠抗疲劳作用研究.江西农业大学学报,2009,31(3):526-529.
    130。颜伟玉,曾星凯,谢国秀等.蜂王浆不同活性组分对大鼠降血脂效果影响.江西农业大学学报,2009,31(5):830-832.
    131.许宝华,谢宪兵,康路妹等.蜂王浆提高动物繁殖性能的研究进展.畜牧与饲料科学,2009,30(9):113-115.
    132.孙丽萍,董捷,王芳.蜂王浆改善心脑血管系统功能的研究.蜜蜂杂志,2002,(1):7-8.
    133.谢宪兵,苏松坤,郑云林等.应用微卫星DNA技术研究中华蜜蜂群内工蜂监督效果.中国农 业科学,2008,41(6):1816-1821.
    134.颜伟玉,Yves Le Conte, Dominique Beslay等.中华蜜蜂幼虫信息素鉴定.中国农业科学.2009,42(6):2250-2254.
    135. Yapar K, Cavusoglu K, Oruc E et al. Protective effect of royal jelly and green tea extracts effect against cisplatin-induced nephrotoxicity in mice:a comparative study. J Med Food,2009,12(5): 1136-1142.
    136. Zhou J. Zhao J, Xue X, et al. Hydrophilic interaction chromatography/tandem mass spectrometry for the determination of melamine in royal jelly and royal jelly lyophilized powder. J Chromatogr B Analyt Technol Biomed Life Sci,2009,877(32):4164-4170.
    137. Yamada N, Yoshimura H. Determinants of chilliness among young women and their application to psychopharmacological trials. Nihon Shinkei Seishin Yakurigaku Zasshi,2009,29(5-6):171-179.
    138 Cavusoqlu K, Yapar K, Yalcin E. Royal jelly (honey bee) is a potential antioxidant against cadmium-induced genotoxicity and oxidative stress in albino mice. J Med Food,2009,12(6): 1286-1292.
    139.杨正.现代养兔.北京:中国农业出版社,1999,122.
    140. Salazar OA, PAZ GV. Screening of Biological Activities Present in Honeybee(Apis Mellifera) Royal Jelly. Toxicology in Vitro,2005,19:645-651.
    141. Barker, S. Royal Jelly. Nature,1959,183:199.
    142.曾志将主编.养蜂学(第二版).北京:中国农业出版社,2009.
    143.郭芳彬.蜂王浆与性激素.养蜂科技,1999,4:29-31.
    144.周景明.李平,霍明东.家兔脱毛的原因及应对措施.中国养兔,2008,4:9-10.
    145. Thornton MJ. The biological actions of estrogens on skin. Exp Dermatol,2002,11(6):487-502.
    146. Yang ZQ, Tu JB, Yao TH, et al. Effects of NGF and estrogens on human hair follicle in vitro. Zhonghua Zheng Xing Wai Ke Za Zhi,2004,20:48-50.
    147.苏哗,敬璞,丁晓雯等.蜂王浆的化学成分、生理活性及应用.农牧产品开发,2000,7:11-12.
    148. Salazar LA, Pazgonzale ZV. Screening of Biological Activities Present in Honeybee (Apis Mellifera) Royal Jelly. Toxicology in Vitro,2005,19:645-651.
    149.郭芳彬.走出蜂王浆会引起性早熟的误区.蜜蜂杂志.1999,11:30.
    150. Liindsay AM, Charming CP. Comparison of the stimulatory effects of bovine, porcine and human follicle-stimulating hormone and of ovine and human luteinizing hormone on the accumulation of cycli cAMP by porcine granulosa cells. Journal of Endocrinology,1979,80:9-20.
    151. Ranniki AS, Zhang FP, Huhtaniemi IT. Ontogeny of follicle stimulating hormone receptor gene expression in the rat testis and ovary. Mol Cell Endocrinol,1995,107:199-208.
    152. Ann E, Drummond G, Anna J, et al. Ovarian estrogen receptorαand β mRNA expression:impact of development and estrogen. Molecular Cellular Endocrinol,1999,149(2):153-61.
    153. Day ML, Geary TW. Handbook of estrous synchronization. Ohio State University Extension Publications. Wooster, Western Regional Publication,2005.
    154. Wu CL, Li YH, Lin HC, et al. Activity and function of rabbit muscle-specific creatine kinase at low temperature by mutation at Gly (268) to Asn (268). Comp Biochem Physiol B Biochem Mol Biol, 2010.
    155. Gatti R, Nigrelli AD, Consadori G, et al. Salmonellosi acuta delconiglio. Riproduzione sperimentate Della malattia. Obietive veterinary,1988,10:33-35.
    156. Saco M, Badiola, Saiz JI, et al. Salmonellosis in a commercial rabbitry. A five year survey from the laboratory and the field perspective. In Proc. Salmonella and salmonellosis 97, Ploufragran, France,1997,387-389.
    157. Zanon F, Siliotto R, Facchin E. Salmonella typhimurium infection in a commercial rabbitry. In proc. 6th world rabbit congress, Toulouse, July 1996,131-133.
    158. Rezende-Neto JB, Rizoli SB, Andrade MV, et al. Rabbit model of uncontrolled hemorrhagic shock and hypotensive resuscitation. Brazilian Journal of Medical and Biological Research,2010,10: 1-9.
    159. Rebollar PG, Bonanno A, Digrigoli A, et al. Endocrine and ovarian response after a 2-day controlled suckling and eCG treatment in lactating rabbit does. Animal Reproduction Science, 2008,104:316-328.
    160. FDA Guidance for industry and reviewers:Estimating the safe starting dose in clinical trials for therapeutics in adult healthy volunteers. U.S. Department of Health and Human Services Food and Drug Administration Canter for Drug Evaluation and Research. July 2005.
    161. Hafez ESE, Hafez B. Reproduction in Farm animals.7th ed. USA:Lippincott Williams Wilkins, 2000.
    162. Bean RJ. Reproduction in the rabbit. American Journal of the Medical Sciences,1926,172(2):261.
    163.谢衷明,毛全福.雌性大鼠离体垂体前叶内在促黄体生成激素释放节律性现象.生理学报,1997,49(6):649-656.
    164. Brann DW, Mahesh VB. Excitatory amino acids:evidence for a role in the control of reproduction and anterior pituitary hormone secretion. Endocr Rev,1997,18:678-700.
    165.关洪斌,李庆章.卵泡刺激素研究进展.东北农业大学学报,2002,33(3):209-212.
    166. Skipper JK, Young LJ, Bergeron JM, et al. Identification of an isofonn of the estrogen receptor messenger RNA lacking exon four and present in the brain. Proc Natl Acad Sci USA,1993,90: 7172.
    167. Barash IA, Cheung CC, Weigle DS, et al. Leptin is a metabolic signal to the reproductive system. Endocrinology,1996,137:3144.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700