Growth patterns of two lines of Angus cattle selected using predicted growth parameters.

Linear functions of body weight and condition score at weaning and 18 mo of age were used to predict the mature weight (A) and maturing rate (k) parameters of an asymptotic growth model of Angus cows at the Subtropical Agricultural Research Station, Brooksville, FL. From 1981 through 1988 a heavy-mature-weight line (Line A) and a rapid-maturing line (Line K) were selected based on predicted A and k values. Linear contrasts (A-K) of least squares means for weight at fixed ages indicated that the weight difference between lines increased from birth to maturity during the period of the study. Animals from Line A were heavier (P less than .01) at all ages. A negative response in maternal ability, relative to increased growth potential of their calves, seems to have occurred in the cows of Line A. Mature weight was reached at approximately 4.5 yr of age in Line K and at approximately 5.5 yr in Line A. Brody's three-parameter and Richards' four-parameter functions were fitted to 2,855 quarterly weights of cows, from birth to 6.5 yr of age, to estimate the average growth curve for each line. Brody's model gave better estimates of weights from 18 mo to maturity, but the asymptotic residual mean squares were slightly higher because early weights were overestimated. Linear and nonlinear regression analyses of weight-age data and comparisons of degree of maturity at different premature ages showed differences in the growth patterns of the two lines selected for early predicted values of A and k.     

Detection of Ehrlichia risticii using an avidin-biotin-immunoperoxidase staining system

An indirect immunoperoxidase procedure using a specific anti-Ehrlichia risticii monoclonal antibody and an avidin-biotin-peroxidase staining method was used to detect E. risticii antigen in infected P388D1 murine monocytes. Several different methods of cytological fixation were used, including acetone (15 min), 95% ethanol (15 min), Bouin's fixative (5 hr), and 10% buffered neutral formalin (24 hr). The E. risticii organisms were labeled effectively and identified in cells fixed with acetone and ethanol. However, infected P388D1 cells fixed in 10% formalin or Bouin's fixative required enzymatic digestion with 1.0% trypsin for 15 min at 37 C before positive results were evident. This indirect immunoperoxidase avidin-biotin staining procedure proved to be a sensitive assay for the detection of intracellular E. risticii and may be an effective diagnostic procedure for formalin-fixed paraffin-embedded tissue.     

马鹿假台鹿采精技术的研究

对６头试验公鹿用假台鹿采精，采精前对特制的假阴道以药用凡士林为滑润剂，注水充气，温度为４０℃±１℃，以适宜的压力和滑润度，将其安装在人工制做的假台鹿内。拨赶公鹿于采精场诱其爬跨。结果，试验的６头公鹿中有４头能够采精，共２２头次，射精量平均每头次１．５４ｍｌ，精子密度为１８．６—３７亿／ｍｌ，精子活力在０．８以上。９３年每头次生产细管冻精１０６．２５支（４２５支／４头次），是同年电刺激采精法平均６４．４支／头次（９０２支／１４头次）的１．６５倍，此法既能采到质量高的精液，又比电采法省工、省时、省力、安全，是一种理想的马鹿采精方法。     

Duration of pituitary and adrenocortical suppression after long-term administration of anti-inflammatory doses of prednisone in dogs.

Duration and magnitude of hypothalamic-pituitary-adrenal axis suppression caused by daily oral administration of a glucocorticoid was investigated, using an anti-inflammatory dose of prednisone. Twelve healthy adult male dogs were given prednisone orally for 35 days (0.55 mg/kg of body weight, q 12 h), and a control group of 6 dogs was given gelatin capsule vehicle. Plasma cortisol (baseline and 2-hour post-ACTH administration) and plasma ACTH and cortisol (baseline and 30-minutes post corticotropin-releasing hormone [CRH] administration) concentrations were monitored biweekly during and after the 35-day treatment period. Baseline plasma ACTH and cortisol and post-ACTH plasma cortisol concentrations were significantly (P less than 0.05) reduced in treated vs control dogs after 14 days of oral prednisone administration. By day 28, baseline ACTH and cortisol concentrations remained significantly (P less than 0.05) reduced and reserve function was markedly (P less than 0.0001) reduced as evidenced by mean post-CRH ACTH, post-CRH cortisol, and post-ACTH cortisol concentrations in treated vs control dogs. Two weeks after termination of daily prednisone administration, significant difference between group means was not evident in baseline ACTH or cortisol values, post-CRH ACTH or cortisol values, or post-ACTH cortisol values, compared with values in controls. Results indicate complete hypothalamic-pituitary-adrenal axis recovery 2 weeks after oral administration of an anti-inflammatory regimen of prednisone given daily for 5 weeks.     

Plant protection problems caused by phytonematodes in Greece1

The major nematode pests of cultivated plants in Greece include root-knot nematodes Meloidogyne spp. (in almost all plants except citrus), cyst-forming nematodes Globodera rostochiensis, G. pallida (in potato), Heterodera avenae (in cereals), Ditylenchus dipsaci (in vegetables and ornamental plants) and Tylenchulus semipenetrans (in citrus). Based on observations made on samples examined at Benaki Phytopathological Institute, it was confirmed that serious infestation of new kiwi orchards with Meloidogyne spp. originated from seedlings infested at the nursery. Also the wide distribution of the nematode Tylenchulus semipenetrans in citrus orchards was mainly attributed to infested seedlings. The above observations led us, in 1985, to the decision to study the nematological fauna of nurseries in Greece.     

Transforming growth factor type beta (TGF-beta) and adipogenesis in pigs

The present study was performed on s.c. adipose tissue of fetal pigs at 35 to 110 d of gestation to examine the distribution of TGF-beta-positive cells, to localize TGF-beta immunoreactivity at the cellular level using electron microscopy (EM), and to determine the effect of TGF-beta on primary cultures of pig adipose tissue cells. Tissues for EM were fixed and embedded in LR white resin. Sections then were incubated with a polyclonal antibody specific for TGF-beta and TGF-beta was located using 20 nm colloidal gold conjugated second antibody. Tissues were fixed and embedded in paraffin for localization of TGF-beta at the light microscope (LM) level. Tissues were incubated with anti-TGF-beta followed by localization using biotinylated second antibody. Using LM, only a few cells stained positively for TGF-beta within developing blood vessels at 35 d. By 50 d, more TGF-beta-positive cells were associated with forming capillary networks. Between 70 d and 110 d, positively stained adipocytes usually were clustered around blood vessels. Cells surrounding hair follicles stained positive for TGF-beta between 90 to 110 d. Electron microscopy revealed TGF-beta labeling within fat cells. Fibroblasts and endothelial cells did not exhibit TGF-beta immunoreactivity. The addition of TGF-beta to primary cultures of s.c. adipose tissue cells from newborn pigs prevented lipid filling in fat cells. This effect was dose-dependent, with half-maximal inhibition occurring at 3 pM maximum inhibition occurred at 40 pM. These results indicate that TGF-beta may regulate angiogenic activity and lipid filling in s.c. adipose tissue of fetal pigs. Although TGF-beta was present in adipocytes and in cells associated with developing capillary networks, the physiological role of TGF-beta during early adipose tissue development is not known.     

Adaptation of 5'-deiodination to hypothyroid conditions following surgical and/or radiothyroidectomy in chickens

The effect of thyroidectomy on serum levels of thyroid hormones (thyroxine, T4; triiodothyronine, T3) and on tissue levels of T3 as well as on 5'-deiodination (5'-DI) in liver, kidney and brain of chickens was investigated. The most effective way of thyroidectomy was a combined surgical (Tx) plus radiothyroidectomy (RTx) with low amounts of 131-I (NaI). The latter destroyed extra-thyroidal hormone production. It was found that even if after Tx and RTx the serum levels of T4 and T3 were close to the detection limit, the tissue T3 level was only half of normal in liver and kidney and remained normal in the brain. It is suggested that lowered 5'-deiodination is an important but not exclusive factor contributing to this adaptation of cells to hypothyroid conditions.