The purpose of this study was to investigate the effect of rapid weight reduction for short duration on serum enzyme and stress hormone in high school wrestlers. Subjects were composed of 7 student wrestlers whose wrestling careers were 3years over. Subjects were reduced 5% of their body weight by exercise, reducing food and sauna method for three days. On the basis of the results analyzed in this study and consideration of many pre studies related it, the result could be drawn as follows. First, Data analysis of 5% weight reduction on CPK, post level revealed more significant increase than pre level(p<.05). Second, Data analysis of 5% weight reduction on LDH, post level revealed more significant increase than pre level(p<.05). Data analysis of 5% weight reduction on Epinephrine, post level revealed more significant decrease than pre level(p<.05). Data analysis of 5% weight reduction on Norepinephrine, post level revealed more significant increase than pre level(p<.05). In conclusion, rapid weight reduction gives an effects on decreasing wrestlers' physical fitness suddenly during the match because of changing rapidly of serum enzyme and stress hormone in the body. I hope that more studies will be followed on serum enzyme and stress hormone in rapid weight reduction of weight class competition players in the future.

본 연구결과 조농비가 다른 사료를 각각 급여한 젖소에 서 임신초기의 유방 크기는 HF군이 LF군 보다 2.4배 가량 유의하게 컸으나, 임신중기와 착유기 동안에는 두 군 간에 차이가 없었다. Estradiol의 혈중농도는 두 군 모두 사춘기 부터 서서히 증가하여 임신기간 동안 사춘기의 2~3.5배가 량이 되었으며, 두 군간 유의한 차이는 나타나지 않았다. 착유기 전 기간에 걸쳐서도 estradiol의 농도는 두 군간 차 이가 없었다. Progesterone의 혈중 농도는 사춘기부터 증가 하기 시작하여 임신중기까지 두 군 모두 비슷한 농도로 유지되었으며, 시험 전 기간에 걸쳐 두 군간 유의한 차이는 없었다. 산유량 4% FCM은 두 군 모두 분만 후 증가하다 LF군은 분만 100일, HF군은 150일을 기점으로 감소하였다. 그러나, 분만 후 50일까지를 제외하고 그 후 전 기간에 걸 쳐 양질 조사료 함량이 높은 사료를 급여한 HF군의 젖소 에서 산유량이 유의하게 높았으며, 분만 250일 까지도 높 은 산유량을 유지하였다. 우유 내 체세포 수는 분만초기를 제외하고 착유기 전 기간 동안 HF군에서 유의하게 감소하 였다. 유지율은 분만 후 비유 초기에 LF군에서 다소 높게 나타났으나, 그 이후부터는 두 군간 차이가 없었으며, 그 밖에 우유 내 단백율, 고형율, MUN 모두 두 군간 차이는 관찰되지 않았다. 산유량과 체세포 수 및 유지율을 기초로 계산한 유대에 있어 HF군이 LF군에 비하여 최고 141.5% 증대되었다. 본 연구결과로부터 젖소의 양질 조사료의 함 량을 적당 수준으로 증가시킴으로써 유방의 크기나 관련 호르몬의 변화 없이 우유의 생산량을 증대시키고 우유의 질을 높일 수 있을 것으로 평가되었다.

Juvenile hormone is the most important hormone inside the insect, but its circulating titer should be under tight control. Then enzymes involved in JH metabolism, especially juvenile hormone esterases (JHEs) play critical roles in insect metamorphosis and reproduction. Within a set of 11 JHEs predicted in the diamondback moth (DBM) genome, Plutlla xylostella (Linn.) we identified one gene that contained the main functional motifs of insect JHEs. Its expression and transcript levels during egg, different instar of larvae, prepuae, pupae and adult stages were measured. Also, its expression in the epidermis, midgut and fatbody of the 4 th instar larvae was compared. The changes in enzyme activity in the 4th instar larvae were determined.

Mullerian inhibiting substance (MIS) is a member of the TGF-β (transforming growth factor-β) family whose members play key roles in development, suppression of tumour growth, and feedback control of the pituitary-gonadal hormone axis. MIS is expressed in a highly tissue-specific manner in which it is restricted to male Sertoli cells and female granulose cells. The serum levels of MIS in prenatal and postnatal ICR mice were measured using the enzymelinked immuno-solvent assay (ELISA) using the MIS/AMH antibody. Mice were grouped by age: the significant periods were at the onset of development. During sex organ differentiation, no remarkable difference between female and male foetus MIS serum levels (both<0.1 ng/ml) was observed. However, MIS serum levels in pregnant mice markedly changed (4.5～12.2 ng/ml). After birth, postnatal female and male mice serum MIS levels changed considerably (male: <0.1～138.5 ng/ml, female: 5.3～103.4 ng/ml), and the changing phase were diametrically opposed (male: decreasing, female: fluctuating). These findings suggest that MIS may have strong associations with not only develop- ment but also puberty. For further studies, establishing the standard MIS serum levels is of importance. Our study provides the basic information for the study of MIS interactions with reproductive organ disability, cancer, and the effect of other hormone or menopause. We hypothesise that if MIS is regularly injected into middle-age women, meno- pause will be delayed. We detected that serum MIS concentration curves change with age. The changing phase is different between males and females, and this difference is significant after birth. Moreover, MIS mRNA is expressed during the developmental period (prenatal) and also in the postnatal period. This finding indicates that MIS may play a significant role in the developmental stage and in growth after birth.

An endoparasitoid wasp, Cotesia plutellae, contains a polydnavirus called C. plutellae bracovirus (CpBV) and induces various physiological alterations of parasitized host along with expressions of viral genes. Two host translation inhibitory factors (HTIFs) encoded in CpBV specifically inhibit host mRNAs at post-transcriptional level. They are expressed in late larval stage of Plutella xylostella parasitized by C. plutellae. To understand their late expression control, promoter region of an HTIF gene called CpBV15α was cloned by inverse PCR. The cloned HTIF upstream region (1,113 bp) possessed a putative JH response element (JHRE) and other promoter elements. The putative promoter region was rejoined with an open reading frame of enhanced green fluorescence protein (EGFP). When the recombinant vector construct was injected into early third instar larvae of nonparasitized P. xylostella, it was expressed in fourth larval instar at 72 h after injection, compared to relatively early expression in 24 h after injection of control construct containing a baculovirus immediate-early promoter. However, recombinant EGFP construct lost the late expression pattern when its promoter region was incomplete by truncating JHRE region. PYR application inhibited EGFP expression of the recombinant construct, but gave little influence on truncated constructs. Interestingly, when the complete promoter construct was injected to pupal stage, its late expression pattern was lost and showed early expression pattern. However, an addition of PYR to pupae, which had been injected with the complete promoter construct, inhibited the reporter gene expression. These results suggest that late expression of a HTIF (CpBV15α) is controlled by its promoter, which is sensitive to host JH titer.

In this study, the toxic effects of fenoxycarb on biological traits of nontarger arthropod P. rosea, Collembola. The tests were assessed in the OECD artificial soil under two different exposure condtions, one was exposed in the bulk soil, and the other was exposed in the compacted soil which unidirectional force was applied to the soil surface. In the bulk system, survived adults and hatched juveniles were counted after 28-day exposures, and in the compact system, survived adults, eggs, hatched juveniles and molts were counted everyday until no more hatching. The toxic effect of fenoxycarb on survival and juvenile production of P. rosea in the bulk system was more toxic than that of the compact system. Juveniles and eggs were seriously affected as compared with toxic effect for adults. Particularly, toxic effect on hatching rate (3.75 mg/kg EC50juvenile) were very higher than that on oviposition (200.868 mg/kg EC50egg) or survival rate of adults ( >1200 mg/kg LC50). The molting freauency of P. rosea was decreased in a concentration dependent manner. These results suggest that the IGRs fenoxycarb exhibit significant impacts on the biological traits of non-target organisms P. rosea and its toxic effects are differently assessed depending on the exposure conditions.

Human growth hormone (hGH), one of the most important hormones in medicine, is secreted from anterior pituitary gland. Its broad physiological function includes body growth, cell regeneration, increasement of muscle volume, bone density, body fat reduction, and so on. Due to the wide range of therapeutic effects, the hGH produced from E. coli has been commercialized already. In this study, we asked whether it is possible to produce recombinant hGH efficiently from various cultured mammalian cells. To meet this purpose, we chose a retrovirus vector system for transfer and expression of the hGH gene in various mammalian cells. Analyses of RT-PCR, ELISA, and Western blot to determine expression of the hGH gene showed the highest production of the hGH was determined from chicken embronic fibroblast (CEF) cells with the concentration of 8.58 μg/ml. The biological activity of the hGH was similar to the commercially available counterpart. These results suggest that mass production of hGH is possible not only in the E. coli but also in the various mammalian cells.

Neuropeptides are the largest group of neurohormones that act in intercellular communication to regulate various physiological and behavioral events during development and reproduction in animals. One of these families is Pyrokinin/PBAN (Pheromone Biosynthesis Activating Neuropeptide) family defined by a similar 5-amino-acid C-terminal sequence (FXPRLamide) that is the active core fragment for these peptides. This motif has been identified from a variety of insect orders, and even a crustacean species. This family of peptides has been implicated in various physiological functions: 1) moth pheromone biosynthesis, 2) larval melanization, 3) moth embryonic and pupal diapause, 4) visceral muscle contraction in the cockroach, 5) fly puparium formation in different insect species. To date, ~159 PBAN/Pyrokinin family peptides have been identified from 40 species. It is one of the largest neuropeptide families in insects; however, the physiological function of most of these peptides is unknown. The mechanism of PBAN control over pheromone production is only well defined for sex pheromone biosynthesis in a limited number of lepidopteran moths. No other insect groups have been reported to regulate pheromone biosynthesis using PBAN. Conventional insecticides target synapses and/or sodium channels that result in neurotoxicity in the nervous system. Unfortunately, this mode of action affects non-target animals as well. These methods remain the major tool for pest control, and the side effects cause many global problems that result in increased environmental and human health expenses. Therefore, we are faced with a requirement to develop new targeted control agents that will lead to pesticides with new modes of action. This is not impossible, but not easy. Every species-specific neuropeptide is expected to play a critical physiological function in metamorphosis and development of insects. There are no exceptions. Our long-standing question is – “how can interference/disruption ofthe insect (neuro)hormonal system be used to discover novel control tools”. To solve this question a novel approach is being applied for finding and screening novel agonist and/or antagonist to gene products, neuropeptide and receptor, from the in vitro system and through virtual modeling. This concept will be a new paradigm opening the window for the next generation of the pest control, and the principle method will be adapted for insect specific pests. Another research interest here will be presented on exocrinal products, such as semiochemicals produced from insects and plants for chemical communication that regulates insect/insect and insect/host interactions. These studies have included the identification of pheromones and the biosynthetic pathway of their production from insects. The ultimate goal of this research is to discover novel biologically-based green pesticides that are environmental-friendly pest control alternatives.

Equine chorionic gonadotropin (eCG) is a heavily glycosylated glycoprotein composed of non-covalently linked α- and β-subunits. To study the function and signal transduction of tethered recombinant-eCG (rec-eCG), a single chain eCG molecule was constructed, and the rec-eCG protein was prepared. In this study, we constructed 5 mutants (Δ1, Δ2, Δ3, Δ4, and Δ5) of rec-eCG using data about known glycoprotein hormones to analyze the role of specific follicle stimulating homone (FSH)-like activity. Three amino acids of certain specific sites were replaced with alanine. The expression vectors were transfected into CHO cells and subjected to G418 selection for 2～3 weeks. The media were collected and the quantity of secreted tethered rec-eCGs was quantified by ELISA. The LH- and FSH-like activities were assayed in terms of cAMP production by rat LH/CG and rat FSH receptors. Then, the metabolic clearance rate analyzed by the injection of rec-eCG (5 IU) into the tail vein was analyzed. The mutant eCGs (Δ1, Δ4, and Δ5) were transcripted, but not translated into proteins. Rec-eCG Δ2 was secreted in much lower amounts than the wild type. Only the rec-eCG Δ3 (β-subunit: Gln94-Ile95-Lys96→Ala94-Ala95-Ala96) was efficiently secreted. Although activity is low, its LH-like activity was similar to that of tethered eCGβα. However, the FSH-like activity of rec-eCGβαΔ3 was completely flat. The result of the analysis of the metabolic clearance rate shoed the persistence of the mutant in the blood until 4 hours after the injection. After then, it almost disappeared at 8 hours. Taken together, these data suggest that 94～96 amino acid sequences in eCG β-subunit appear to be of utmost importance for signal transduction of the FSH receptor.

The objective of this study was to examine the effect of eCG and various concentrations (20, 40, and 80 ) of porcine FSH on nuclear maturation and intracellular glutathione (GSH) level of oocytes, and embryonic development after parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT) in pigs. Immature pig oocytes were matured in TCM-199 supplemented with porcine follicular fluid, cysteine, pyruvate, EGF, insulin, and hormones (10 IU/ml hCG and 10 IU/ml eCG or FSH) for the first 22 h and then further cultured in hormone-tree medium for an additional 22 h. Nuclear maturation of oocytes () was not influencem foreCG and various concentrations FSH. Embryonic development to the cleavage stage () and mean number of cells in blastocyst ( cells) after PA were not altered but blastocyst formation e-treignificaddlor(p<0.05) improvem forthe supplementation eith 80 FSHr(64%) compared to 47%, io8%, iand 47% in oocytes that were treated with eCG, 20,i and 40 FSH,i numectivelo. In SCNT, fusion () of cell-cytoplast couplets and siosequent embryo cleavage () were not influencem fordifferent gonadotropins but blastocyst formation tended to increase forthe supplementation eith 80 FSHr(25% vs. ). Our nuults demonstrated that oocyte maturation and embryonic development after PA and SCNT e-frinfluencem fortype of gcem fortype of gits concentration. In this study, supplementation of maturation medium eith 80 FSHrimproved preimplantation development of PA and SCNT pig embryos, probably by increasing intracellular GSH concentration of matured oocytes.

Ovarian cancer is a significant cause of cancer-related death in women, but the main biological causes remain open questions. Hormonal factors have been considered to be an important determinant causing ovarian cancer. Recent studies have shown that gonadotropin-releasing hormone (GnRH)-I and its analogs have clinically therapeutic value in the treatment of ovarian cancer. In addition, numerous studies have shown that the potential of GnRH-II in normal reproductive system or reproductive disorder. GnRH-I receptors have been detected in approximately 80% of ovarian cancer biopsy specimens as well as normal ovarian epithelial cells and immortalized ovarian surface epithelium cells. GnRH-II receptors have also been found to be more widely expressed than GnRH-I receptors in mammals, suggesting that GnRH receptors may have additional functions in reproductive system including ovarian cancer. The signal transduction pathway following the binding of GnRH to GnRH receptor has been extensively studied. The activation of protein kinase A/C (PKA/PKC) pathway is involved in the GnRH-I induced anti-proliferative effect in ovarian cancer cells. In addition, GnRH-I induced mitogen-activated protein kinase (MAPK) activation plays a role in anti-proliferative effect and apoptosis in ovarian cancer cells and the activation of transcriptional factors related to cellular responses. However, the role of GnRH-I and II receptors, there are discrepancies between previous reports. In this review, the role of GnRH in ovarian cancer and the mechanisms to induce anti-proliferation were evaluated.

This study examined pregnancy and fetal loss rates according to different estrus synchronization protocols and injection of gonadotropin releasing hormone (GnRH) after transfer of Korean Native Cattle embryos to Holstein recipients. In Experiment 1, recipients received no treatment (Control, n = 119); two injections of prostaglandin ( ) 11 days apart (PGF group, n = 120); GnRH (day 0)- (day 7)-GnRH (day 9) (Ovsynch group, n = 120); and CIDR (day 0)- and CIDR removal (day 7)-GnRH (day 9) (CIDR group, n = 110). In Experiment 2, the control group was received no treatment of GnRH. The treatment groups were received GnRH at embryo transfer (ET) (day 0), 7 days later, 14 days later, ET and 7 days later, 7 and 14 days later, or ET, 7 and 14 days later. Recipients were assigned to treatment randomly and received two in vitro produced blastocysts. Pregnancy was diagnosed at day 60 by palpation per rectum. Fetal loss to term was determined by palpation every 90 days thereafter. In Experiment 1, the pregnancy rate in the CIDR group (59.1%) were higher than in the Control group (42.0%) (p<0.01); fetal loss rates were similar for all groups (12.0 to 18.5%). In Experiment 2, the pregnancy rate in Day 0+7+14 group was higher (60.2%) than the control (40.2%) (p<0.01) and resulted in a lower fetal loss (p<0.05) than the control (4.6 vs. 11.4%). There were no significant difference between other treatment and the control (p>0.05). These results show that pregnancy rates of bovine embryos can be enhanced by CIDR insertion or GnRH treatment. Additionally, fetal loss may be reduced with GnRH treatment after ET.

The objective of this study is to investigate the changes in concentrations of blood urea nitrogen (BUN) and sex steroid hormones, such as estrogen, progesterone, and testosterone in Korean cattle (Hanwoo) with reproductive disorders and to examine the relationship between BUN and body condition score (BCS) in Hanwoo. The concentration of BUN was 16.2 mg/dl, 17.8 mg/dl, 15.1 mg/dl, 17.9 mg/dl, and 28.3mg/dl in pregnancy, repeat breeding, follicular cyst, luteal cyst, and ovarian atrophy, respectively. In Hanwoo with BCS , and , the concentration of BUN was 15.8 mg/dl, 17.0 mg/dl, and 17.6 mg/dl, respectively. Fluoroimmunoassay showed that serum estrogen and progesterone levels were decreased in reproductive disorders Hanwoo, such as ovarian atrophy, endometritis, and weak estrus. The testosterone level was significantly decreased in Hanwoo with reproductive disorders compared to that in pregnant Hanwoo ( vs 0.13 ng/ml, p<0.05). The progesterone and estrogen concentrations in follicular fluid obtained from ovary with follicular cyst were significantly higher (p<0.05) than those in normal follicle fluid. These results show that there is no relationship between BUN and BCS in Hanwoo, and the concentration of sex steroid hormone in serum and follicular fluid are changed in reproductive disorders Hanwoo.