Effect of a single injection of gonadotropin-releasing hormone (GnRH) and human chorionic gonadotropin (hCG) on testicular blood flow measured by color doppler ultrasonography in male Shiba goats     

Haney SAMIR  Kazuaki SASAKI  Eman AHMED  Aly KAREN  Kentaro NAGAOKA  Mohamed EL SAYED  Kazuyoshi TAYA  Gen WATANABE 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2015,77(5):549-556

Although color Doppler ultrasonography has been used to evaluate testicular blood flow in many species, very little has been done in goat. Eight male Shiba goats were exposed to a single intramuscular injection of either gonadotropin-releasing hormone (GnRH group; 1 µg/kg BW) or human chorionic gonadotropin (hCG group; 25 IU/kg BW). Plasma testosterone (T), estradiol (E2) and inhibin (INH) were measured just before (0 hr) and at different intervals post injection by radioimmunoassay. Testis volume (TV) and Doppler indices, such as resistive index (RI) and pulsatility index (PI) of the supratesticular artery, were measured by B-mode and color Doppler ultrasonography, respectively. The results indicated an increase in testicular blood flow in both groups, as RI and PI decreased significantly (P<0.05), but this increase was significant higher and earlier in hCG group (1 hr) than in the GnRH group (2 hr). A high correlation was found for RI and PI with both T (RI, r= −0.862; PI, r= −0.707) and INH in the GnRH group (RI, r=0.661; PI, r=0.701). However, a significant (P<0.05) correlation was found between E2 and both RI (r= −0.610) and PI (r= −0.763) in hCG group. In addition, TV significantly increased and was highly correlated with RI in both groups (GnRH, r= −0.718; hCG, r= −0.779). In conclusion, hCG and GnRH may improve testicular blood flow and TV in Shiba goats.  相似文献   

Accessory corpora lutea formation in pregnant Hokkaido sika deer (Cervus nippon yesoensis) investigated by examination of ovarian dynamics and steroid hormone concentrations     

Yojiro YANAGAWA  Yukiko MATSUURA  Masatsugu SUZUKI  Shin-ichi SAGA  Hideto OKUYAMA  Daisuke FUKUI  Gen BANDO  Masashi NAGANO  Seiji KATAGIRI  Yoshiyuki TAKAHASHI  Toshio TSUBOTA 《The Journal of reproduction and development》2015,61(1):61-66

Generally, sika deer conceive a single fetus, but approximately 80% of pregnant females have two corpora lutea (CLs). The function of the accessory CL (ACL) is unknown; moreover, the process of ACL formation is unclear, and understanding this is necessary to know its role. To elucidate the process of ACL formation, the ovarian dynamics of six adult Hokkaido sika deer females were examined ultrasonographically together with peripheral estradiol-17β and progesterone concentrations. ACLs formed in three females that conceived at the first estrus of the breeding season, but not in those females that conceived at the second estrus. After copulation, postconception ovulation of the dominant follicle of the first wave is induced by an increase in estradiol-17β, which leads to formation of an ACL. A relatively low concentration of progesterone after the first estrus of the breeding season is considered to be responsible for the increase in estradiol-17β after copulation.  相似文献   

Estrogen suppresses melatonin-enhanced hyperactivation of hamster spermatozoa     

Masakatsu FUJINOKI  Gen L. TAKEI 《The Journal of reproduction and development》2015,61(4):287-295

Hamster sperm hyperactivation is enhanced by progesterone, and this progesterone-enhanced hyperactivation is suppressed by 17β-estradiol (17βE₂) and γ-aminobutyric acid (GABA). Although it has been indicated that melatonin also enhances hyperactivation, it is unknown whether melatonin-enhanced hyperactivation is also suppressed by 17βE₂ and GABA. In the present study, melatonin-enhanced hyperactivation was significantly suppressed by 17βE₂ but not by GABA. Moreover, suppression of melatonin-enhanced hyperactivation by 17βE₂ occurred through non-genomic regulation via the estrogen receptor (ER). These results suggest that enhancement of hyperactivation is regulated by melatonin and 17βE₂ through non-genomic regulation.  相似文献   

Different effects of an extended photoperiod treatment on growth,gonadal function,and condition of hair coats in Thoroughbred yearlings reared under different climate conditions     

Tsuyoshi SUZUKI  Hirotoshi MIZUKAMI  Yasuo NAMBO  Mutsuki ISHIMARU  Kenji MIYATA  Kentaro AKIYAMA  Kenji KOROSUE  Hiroshi NAITO  Kentaro NAGAOKA  Gen WATANABE  Kazuyoshi TAYA 《Journal of Equine Science》2015,26(4):113-124

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Estimating aboveground carbon using airborne LiDAR in Cambodian tropical seasonal forests for REDD+ implementation     

Tetsuji Ota  Tsuyoshi Kajisa  Nobuya Mizoue  Shigejiro Yoshida  Gen Takao  Yasumasa Hirata  Naoyuki Furuya  Takio Sano  Raul Ponce-Hernandez  Oumer S. Ahmed  Heng Sokh  Vuthy Ma  Eriko Ito  Jumpei Toriyama  Yukako Monda  Hideki Saito  Yoshiyuki Kiyono  Sophal Chann  Nang Ket 《Journal of Forest Research》2015,20(6):484-492

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Evaluation of larval growth process and bamboo consumption of the bamboo powder-post beetle Dinoderus minutus using X-ray computed tomography     

Hiroki Watanabe  Yoshiyuki Yanase  Yoshihisa Fujii 《Journal of Wood Science》2015,61(2):171-177

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Specific detection of potentially allergenic kiwifruit in foods using polymerase chain reaction     

Taguchi H  Watanabe S  Hirao T  Akiyama H  Sakai S  Watanabe T  Matsuda R  Urisu A  Maitani T 《Journal of agricultural and food chemistry》2007,55(5):1649-1655

Kiwifruit (Actinidia deliciosa and Actinidia chinensis) is allergenic to sensitive patients, and, under Japanese regulations, it is one of the food items that are recommended to be declared on food labeling as much as possible. To develop PCR-based methods for the detection of trace amounts of kiwifruit in foods, two primer pairs targeting the ITS-1 region of the Actinidia spp. were designed using PCR simulation software. On the basis of the known distribution of a major kiwifruit allergen (actinidin) within the Actinidia spp., as well as of reports on clinical and immunological cross-reactivities, one of the primer pairs was designed to detect all Actinidia spp. and the other to detect commercially grown Actinidia spp. (i.e., kiwifruit, Actinidia arguta, and their interspecific hybrids) except for Actinidia polygama. The specificity of the developed methods using the designed primer pairs was verified by performing PCR experiments on 8 Actinidia spp. and 26 other plants including fruits. The methods were considered to be specific enough to yield target-size products only from the target Actinidia spp. and to detect no target-size products from nontarget species. The methods were sensitive enough to detect 5-50 fg of Actinidia spp. DNA spiked in 50 ng of salmon testis DNA used as a carrier (1-10 ppm of kiwifruit DNA) and 1700 ppm (w/w) of fresh kiwifruit puree spiked in a commercial plain yogurt (corresponding to ca. 10 ppm of kiwifruit protein). These methods would be expected to be useful in the detection of hidden kiwifruit and its related species in processed foods.  相似文献   

Determination of theaflavins including methylated theaflavins in black tea leaves by solid-phase extraction and HPLC analysis     

Nishimura M  Ishiyama K  Watanabe A  Kawano S  Miyase T  Sano M 《Journal of agricultural and food chemistry》2007,55(18):7252-7257

A quantitative method for four theaflavins and two methylated theaflavin derivatives in black tea leaves was developed by solid-phase extraction and a high-performance liquid chromatographic method with photodiode array detection. The theaflavins in black tea leaves were extracted three times with 40 vol 50% aqueous ethanol (mg dry tea powder/mL) containing 2% ascorbic acid. The ethanol extracts were diluted 4-fold with distilled water. All diluted extracts were directly applied to the solid-phase C18 cartridge column without concentration. The fraction of theaflavins was obtained by 40% ethanol extraction after rinsing with water followed with 15% ethanol extraction. An aliquot of theaflavins after concentration was injected onto an ODS C18 reversed-phase column, and four theaflavins and two methylated theaflavins were sufficiently separated by a linear gradient system using distilled water and acetonitrile with 0.5% acetic acid. This analytical method is sensitive for the determination of a small amount of methylated theaflavins, since various interfering substances produced during the fermentation process were eliminated in advance by solid-phase extraction. Using this analytical method, we also demonstrated that methylated theaflavins were easily produced during the manufacture of black tea.  相似文献   

Bioavailability of amino acid-chelated and glass-embedded manganese to rainbow trout, Oncorhynchus mykiss (Walbaum), fingerlings     

S Satoh  M J Apines  T Tsukioka  V Kiron  T Watanabe  & S Fujita 《Aquaculture Research》2001,32(S1):18-25

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Rearing of squid hatchlings, Heterololigo bleekeri (Keferstein 1866) up to 2 months in a closed seawater system     

Yuzuru Ikeda  Ikuko Sakurazawa  Kingo Ito  Yasunori Sakurai  & Gen Matsumoto 《Aquaculture Research》2005,36(4):409-412

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