Efficacy of IV theophylline in children with severe status asthmaticus.

STUDY OBJECTIVE: To determine whether adding IV theophylline to an aggressive regimen of inhaled and IV beta-agonists, inhaled ipratropium, and IV methylprednisolone would enhance the recovery of children with severe status asthmaticus admitted to the pediatric ICU (PICU). DESIGN: A prospective, randomized, controlled trial. Asthma scoring was performed by investigators not involved in treatment decisions and blinded to group assignment. SETTING: The PICU of an urban, university-affiliated, tertiary-care children's hospital. PATIENTS: Children with a diagnosis of status asthmaticus who were admitted to the PICU for < or = 2 h and who were in severe distress, as indicated by a modified Wood-Downes clinical asthma score (CAS) of > or = 5. INTERVENTIONS: All subjects initially received continuous albuterol nebulizations; intermittent, inhaled ipratropium; and IV methylprednisolone. The theophylline group was also administered infusions of IV theophylline to achieve serum concentrations of 12 to 17 microg/mL. A CAS was tabulated twice daily. MEASUREMENTS AND RESULTS: Forty-seven children (median age, 8.3 years; range, 13 months to 17 years) completed the study. Twenty-three children received theophylline. The baseline CASs of both groups were similar and included three subjects receiving mechanical ventilation in each group. All subjects receiving mechanical ventilation and theophylline were intubated before drug infusion. Among the 41 subjects who were not receiving mechanical ventilation, those receiving theophylline achieved a CAS of < or = 3 sooner than control subjects (18.6 +/- 2.7 h vs 31.1 +/- 4.5 h; p < 0.05). Theophylline had no effect on the length of PICU stay or the total incidence of side effects. Subjects receiving theophylline had more emesis (p < 0.05), and control patients had more tremor (p < 0.05). CONCLUSIONS: Theophylline safely hastened the recovery of children in severe status asthmaticus who were also receiving albuterol, ipratropium, and methylprednisolone. The role of theophylline in the management of asthmatic children in impending respiratory failure should be reexamined.

Interactions between environmental temperature and porcine growth hormone (pGH) treatment in neonatal pigs.

Age-dependent interactions between environmental temperature and porcine growth hormone (pGH) treatment on the function of the somatotrophic axis were evaluated in the neonatal pig. At 3 d of age, 40 Landrace x Yorkshire x Duroc piglets received intraperitoneal implants containing either recombinant pGH (0.5 mg/d; n = 20) or vehicle (control; n = 20). Piglets were maintained at either a low (21 degrees C, 50% relative humidity; n = 20) or high (32 degrees C, 50% relative humidity; n = 20) temperature. At 4 and 6 wk of age, 5 pGH-treated and 5 control piglets from each thermal group were sacrificed for tissue collection. Blood samples were collected at the time of sacrifice and analyzed for serum concentrations of GH, insulin-like growth factor 1 (IGF-1), and IGF-2. Liver RNA was analyzed for mRNAs specific for the GH receptor, IGF-1, IGF-2, and IGF binding protein 3. There was no effect of pGH treatment (P = 0.4) on average daily gain; however, both age (P = 0.002) and temperature (P = 0.001) had an effect on average daily gain such that those animals maintained at a low temperature and those sacrificed at 6 wk had greater average daily gains. Serum concentration of GH was elevated (P = 0.003) by pGH treatment and was lowest in the 6-wk-old group (P = 0.008). Serum concentration of IGF-1 was elevated (P = 0.007) by pGH treatment and increased with age (P = 0.01). Liver GH receptor mRNA was unaffected (P > 0.5) by pGH treatment, but was greater in the 6-wk-old group (P < 0.0001) and in piglets maintained at the high temperature (P = 0.04). IGF-1 mRNA was enhanced by pGH treatment (P = 0.0003) and by exposure to the high temperature (P = 0.04), but did not differ (P > 0.5) between age groups. IGF-2 mRNA was greater (P = 0.0009) in the 4-wk-old group and in piglets maintained at the high temperature (P = 0.007), but was unaffected (P = 0.5) by pGH treatment. IGF binding protein 3 mRNA increased with age (P = 0.0004) and was stimulated by pGH treatment in the 6-wk-old group (P = 0.034). The relatively lower level of GH receptor and IGF mRNAs in conjunction with greater growth in the cold environment suggests that somatotrophic gene expression in the liver is not rate limiting for growth in the neonatal pig.

Membranous glomerulonephritis associated with Graves' disease.

Renal involvement in thyroid diseases is an unusual event. Antineutrophil cytoplasmic antibody (ANCA) associated vasculitis has been reported in propylthiouracil-treated patients. Membranous glomerulonephritis has been reported in association with both antithyroglobulin and thyroid antimicrosomal antibodies. The development of membranous glomerulonephritis may be associated with administration of 131I. We present a patient who developed membranous glomerulonephritis after administration of 131I. The clinical and pathological features of renal involvement in thyroid diseases are reviewed.

Effects of thermal environment on response to acute peripheral lipopolysaccharide challenge exposure in neonatal pigs.

OBJECTIVE: To evaluate effects of thermal environment on response to acute peripheral lipopolysaccharide (LPS) challenge exposure in neonatal pigs. ANIMALS: 26 neonatal pigs. PROCEDURE: Pigs were assigned to the following treatment groups: 1 warm environment/LPS; 2 warm environment/saline solution; 3 cool environment/LPS; and 4 cool environment/saline solution. For each pig given LPS, 1 littermate of the same sex was given saline solution. Sows with baby pigs were housed in a warm (32 C) or cool (21 C) thermal environment. At 28 days of age, pigs were given 150 micrograms/kg of body weight of Escherichia coli LPS or saline solution intraperitonealy as a control. Rectal temperature and signs of sickness were monitored for 3 hours after LPS administration, when pigs were euthanatized and blood samples were collected to determine serum concentrations of tumor necrosis factor (TNF) alpha and cortisol. To determine in vitro production of TNF alpha, alveolar macrophages were collected by tracheal lavage and incubated for 24 hours at 37 or 41 C, with or without LPS (10 micrograms/ml). RESULTS: Thermal environment had a significant (P = 0.0004) effect on rectal temperature; LPS administration induced a febrile response (P = 0.0007) only in pigs in the warm environment. All LPS-injected pigs developed signs of endotoxemia; serum TNF alpha and cortisol concentrations were significantly increased (TNF alpha, P = 0.003; cortisol, P = 0.0001); there was no significant in vivo thermal effect on serum TNF alpha and cortisol concentrations. LPS-stimulated alveolar macrophages produced significantly less (P = 0.0086) TNF alpha when incubated at 41 C. CONCLUSIONS: Thermal environment can have a significant impact on the response of neonatal pigs exposed to bacterial endotoxins.

Suppression of somatotroph function induced by growth hormone treatment in neonatal pigs.

The effect of recombinant porcine growth hormone (pGH) treatment on pituitary function was evaluated in young pigs. Piglets received intraperitoneal recombinant pGH implants (0.5 mg/d sustained release) or vehicle implants beginning at 3 d of age. Ten piglets were sacrificed at 4 and 6 wk of age (five piglets/treatment group) for the collection of pituitary glands, blood, and liver tissue. Blood samples also were drawn at 3 and 12 d of age. Serum concentrations of GH, prolactin (PRL), thyroid-stimulating hormone (TSH), insulin-like growth factor-1 (IGF-1) and IGF-2 were evaluated. Levels of IGF-1 and IGF-2 mRNA were determined in liver samples. Treatment with GH increased circulating levels of GH and IGF-1 (P < 0.01), but not PRL, TSH, or IGF-2. Hepatic IGF-1, but not IGF-2, mRNA levels were increased by pGH (P < 0.001). Cultured pituitary cells from each animal were challenged with 0.1, 1, and 10 nM GH-releasing hormone (GHRH); 2 nM 8-Br-cAMP; or 100 nM phorbol myristate acetate. The release of GH from cultured pituitary cells was stimulated by all secretagogues (P < 0.001). The secretion of GH, but not PRL or TSH, in culture was inhibited by previous in vivo GH treatment (P < 0.001). Similarly, cellular GH, but not PRL or TSH, content was lower in the GH-implant group (P = 0.005). Cell cultures from 6-wk-old piglets secreted more GH, but not PRL or TSH, than cultures from 4-wk-old piglets (P < 0.05). Likewise, cellular GH, but not PRL or TSH, content was greatest in cultures from 6-wk-old animals (P = 0.002). Piglet growth was not affected by exogenous GH treatment (P = 0.67). These results demonstrate that exogenous pGH treatment selectively down-regulates somatotroph function in young pigs.

Expression of luteinizing hormone-releasing hormone and its receptor in porcine immune tissues.

Luteinizing hormone-releasing hormone (LHRH) is the primary regulator of pituitary LH release. However, LHRH has also been identified in extrahypothalamic sites including immune tissues. Accordingly, immunomodulatory properties for LHRH have been suggested. We wanted to determine whether LHRH and its receptor are produced by immune tissues in the pig. First, a cDNA was cloned and sequenced from the porcine hypothalamus that showed 87.5% homology with the human LHRH gene. Internal primers were identified from this sequence for amplifying a 268 bp product by PCR. In addition to the hypothalamus, PCR products reflecting LHRH mRNA were amplified in porcine spleen, thymus, and peripheral blood lymphocyte (PBL) cDNA. LHRH mRNA was not detected in liver, cerebral cortex, or pituitary tissue samples. Primers were designed to amplify a 360 bp fragment of LHRH-receptor cDNA. PCR products reflecting LHRH-receptor mRNA were amplified in pig hypothalamus, pituitary, thymus, spleen and PBL cDNA samples. No such products were amplified in cortex and liver samples. In summary, we report the sequence of a cDNA coding for LHRH and Gonadotropin-RH associated peptide (GAP) in the pig hypothalamus. Additionally, we provide evidence that LHRH and its receptor are synthesized in porcine immune tissues. This leads us to speculate that LHRH may have local, immunomodulatory functions in pigs.

Effects of individual vs group penning on the performance of weanling pigs.

Two experiments (five trials) were conducted to determine the effects of individual vs group penning on the performance of 4-wk-old crossbred barrows and gilts. In each experiment, half the pigs were tested in a group pen (four pigs) for two 7-d periods and individually for one 7-d period and the other pigs were fed individually for two periods and as a group for one period. In Exp. 1 (two trials, each with five replicates of eight pigs), individually penned pigs had physical and visual contact with pigs in the adjoining pens; in Exp. 2 (three trials, each with five replicates of eight pigs), such contact was denied. Growth rate, feed intake, and feed efficiency were determined at the end of each period. In addition, during Trial 3 of Exp. 2 blood samples were collected at the end of each period and plasma was assayed for cortisol and triiodothyronine (T3) concentrations. Penning sequences produced inconsistent weight gains and feed intake. Differences in gain favored (P < .04) the individually penned pigs during Trial 3 of Exp. 2 and differences in feed intake favored the individually penned pigs during Trial 2 of Exp. 1 (P < .009) and during Trials 2 and 3 of Exp. 2 (P < .02 and P < .009, respectively). Penning treatment had no effect on feed efficiency, plasma cortisol, or T3 concentrations. These data suggest that pigs perform equally well whether fed and housed individually or in groups, with no indications of stress associated with individual pens and isolation.

Gonadotroph function in 3-week-old gilts reared in a warm or cool thermal environment.

The present study evaluated the effect of a warm (cycling 27-32 degrees C, 50-70% RH) or cool (21 degrees C, 55% RH) thermal environment (TE) on gonadotroph function in 3-week-old gilts (females). Pituitary cells from twelve gilts reared in each TE were cultured at a density of 250,000 cells/1 ml well and exposed to vehicle (culture medium); 1,1, and 10 nM gonadotropin-releasing hormone (GnRH); 2 mM 8-Br-cAMP (cAMP); and 100 nM phorbol myristate acetate (PMA). Luteinizing hormone (LH) and follicle-stimulating hormone (FSH) secretion in culture were stimulated by GnRH and by pharmacological compounds (p < .0001). In vitro LH secretion was approximately three-fold higher in the warm, compared to the cool, TE group (p < .0001). Similarly, cellular LH content in the warm TE exceeded that in the cool TE (p < .005). The in vitro secretion of FSH and cellular FSH content were significantly elevated in the warm TE (p < .02). Serum LH concentrations in the warm and cool TE were 7.01 +/- 1.75 and 2.13 +/- .44 ng/ml, respectively (p < .02). Serum FSH concentrations were 6.38 +/- .53 and 4.59 +/- .28 ng/ml in the warm and cool TE, respectively (p < .01). The results of this study demonstrate that secretory responses of gonadotrophs in early postweaning pigs are influenced by chronic TE exposure. These differences in secretory activity may reflect levels of cellular gonadotropin available for release.

Lactotroph and somatotroph function in piglets reared in a constant hot environment.

The present study evaluated the effect of rearing in a constant hot (32 degrees C) or cool (21 degrees C) thermal environment (TE) on lactotroph and somatotroph secretory activity in 5-wk-old barrows (castrate males) and gilts (female). Pituitary cells from seven gilts and seven barrows from each TE were cultured at a density of 250,000 cells/1 ml well and exposed to vehicle (culture medium); .1, 1, 10, or 100 nM thyrotropin-releasing hormone (TRH); or .1, 1, or 10 nM growth hormone-releasing hormone (GHRH). Post-receptor cellular stimulation was induced pharmacologically with 2 mM 8-Br-cAMP (cAMP); 100 nM phorbol myristate acetate (PMA); or 59 mM KCl. Prolactin secretion in culture was stimulated by TRH and by pharmacological compounds (p < .0001). In vitro PRL secretion was increased approximately two-fold in the hot environment (p < .02). Similarly, cellular PRL content in the hot TE was twice that in the cool TE (p < .01). The in vitro secretion of growth hormone (GH) was increased by GHRH and by pharmacological compounds (p < .0001), but was unaffected by TE (p > .5). No effects of sex (p > .3) or sex x TE interactions (p > .2) were detected in any endpoint. The results of this study demonstrate that lactotroph, but not somatotroph, secretory activity is enhanced by a constant hot TE in early postweaning pigs. This increase in secretory activity does not appear to be dependent on receptor-mediated cellular activation, but may reflect enhanced levels of cellular PRL available for release.

Effects of feeding fumonisin B1 in lactating sows and their suckling pigs.

The mycotoxin fumonisin B1 (FB1) produced by Fusarium moniliforme in corn causes pulmonary edema in finishing swine. Effects of lower nonlethal amounts and effects in lactating sows with suckling pigs are unknown. An initial study was conducted to determine a nonlethal concentration of FB1 for lactating sows; whether ingested FB1 could be detected in the milk; and whether toxicosis could be detected in the pigs, as determined by necropsy. Another study was conducted to determine toxicosis in the pigs by measuring liver sphinganine-to-sphingosine ratio, and whether ingested FB1 affected T-lymphocyte function in sows and their pigs. Furthermore, sows of this study were maintained in controlled hot (27 to 32 C, 50 to 70% relative humidity) and thermoneutral (21 C, 55% relative humidity) environments to determine whether high temperature exacerbated the effects of FB1. In the first study, 100 micrograms of FB1/g of corn soybean meal diet was found to be nonlethal when fed for 14 days. Fumonisin B1 was not detected in the milk at 30 ppb and lesions were not found in the necropsied pigs, including 1 from a sow that died of porcine pulmonary edema syndrome after ingesting FB1 at a concentration of 175 ppm. In the second study, differences in liver sphinganine-to-sphingosine ratio of pigs were not found. Expressions of cell surface antigens on blood lymphocytes and lymphocyte proliferation response to various mitogens were not affected by FB1 or high temperature in sows or their pigs.(ABSTRACT TRUNCATED AT 250 WORDS)

Somatotroph, lactotroph and thyrotroph function in three-week-old gilts reared in a hot or cool environment.

The influence of the thermal environment on the ability of the pituitary gland to secrete growth hormone (GH), prolactin (PRL), and thyroid-stimulating hormone (TSH) was examined in gilts reared under hot (H: 27-32 degrees C, 50-90% RH, n = 6) or cool (C: 20 degrees C, 50% RH, n = 6) conditions. Piglets were sacrificed at 3 wks of age. Pituitary cells from each animal were cultured and exposed to vehicle (culture medium); 1, 1, and 10 nM thyrotropin-releasing hormone (TRH); .1, 1, and 10 nM growth hormone-releasing hormone (GHRH); 59 mM KCl; 2 mM 8-Br-cAMP; and 100 nM phorbol myristate acetate. Rearing in the H, compared to the C, environment increased plasma PRL concentrations (p < .001), in vitro PRL secretion subsequent to all secretagogue treatments (p < .001), and cellular PRL content (p < .001). The stimulated release of TSH in culture was reduced (p < .001), but cellular TSH content was increased (p < .05) by exposure to the H environment. The total amount of TSH in culture (secreted + cellular) was not affected by thermal environment. The release of GH in vitro, cellular GH content, total GH in culture, and plasma GH concentrations were similar between H and C groups. The only dose-response curves that differed in slope between thermal groups were those produced by the TSH response to TRH (p < .001). The results of this study suggest that chronic exposure to a hot environment can 1) enhance PRL secretion by a mechanism which affects the quantity of releasable PRL rather than lactotroph sensitivity to secretagogues and 2) reduce TSH secretion by inhibiting thyrotroph secretory response to stimulation.

The effects of diets formulated on an ideal protein basis on growth performance, carcass characteristics, and thermal balance of finishing gilts housed in a hot, diurnal environment.

Forty-eight finishing gilts (initial BW = 70.6 +/- .95 kg) were randomly assigned to one of eight experimental treatments in a 2 x 2 x 2 factorial arrangement with main effects including dietary lysine (.60 vs 1.00%), source of amino acid fortification (intact protein vs synthetic amino acids formulated on an ideal protein basis), and environmental temperature (thermoneutral [TN]: 20 degrees C vs hot, diurnal [HD]: 27.7 to 35 degrees C). The ideal protein diets were formulated by using corn and soybean meal to meet the fifth-limiting amino acid; synthetic lysine, threonine, tryptophan, methionine, or isoleucine were added to meet the gilts' estimated requirements. The ratios of other total amino acids relative to lysine were as follows: threonine, 66%; tryptophan, 17%; methionine and cystine, 56%; and isoleucine, 63%. Average daily gain, ADFI, and feed efficiency (G/F) were similar for gilts fed the intact and those fed the ideal proteins diets (P > .10). Increasing dietary lysine improved d 0 to 14 ADG (P < .01), but no differences were observed for the overall experiment. Gilts in the HD environment ate less feed and had lower ADG than gilts in the TN environment (P < .01). A temperature x lysine interaction was observed (P < .02) for G/F. Increasing dietary lysine had no effect on G/F of gilts in the TN environment but improved G/F of gilts in the HD environment. Gilts fed the intact protein diets had higher (P < .01) N intake and plasma urea concentrations. Gilts fed the ideal protein diets had lower (P < .05) plasma essential amino acids, with the exception of lysine. Carcass protein and lipid contents were improved (P < .01) for gilts in the HD environment and for those fed 1.00% lysine. Backfat thickness and longissimus muscle area (P < .01) were improved and lipid accretion rate tended to decrease (P < .08) in gilts fed 1.00% lysine. The source of amino acid fortification did not influence carcass characteristics (P > .10). Rectal, skin, and ear temperatures were higher for gilts in the HD environment (P < .05). Metabolic heat production was elevated by feeding gilts the ideal protein diets (P < .03). In conclusion, increased dietary lysine improved G/F and carcass leanness in gilts to a greater extent in HD than in TN environments. However, no improvements in growth performance or carcass traits resulted from feeding ideal protein diets.

Somatotroph and lactotroph function in relation to growth in six-week-old pigs reared in a hot or cool environment.

The influences of thermal environment and individual growth rate on somatotroph and lactotroph function were examined in 6-week-old barrows reared entirely in a hot (H: 27-32 degrees C, n = 8) or cool (C: 21 degrees C, n = 10) environment. Growth hormone (GH) and prolactin (PRL) cell contents and responses to growth hormone-releasing hormone (GHRH) or thyrotropin-releasing hormone (TRH) were evaluated in cultured pituitary cells from each animal. Plasma GH, PRL, and insulin-like growth factor-1 (IGF-1) concentrations also were monitored. Thermal environment did not affect in vitro GH secretion, cellular GH content, or plasma GH concentrations. Stimulated in vitro GH release (GHRH-basal) and plasma GH were inversely related to average daily gain (ADG, r = -.76, p < .005 and r = -.51, p < .05, respectively). Cellular GH content also declined as ADG increased (r = -.57, p < .05). Plasma IGF-1 concentrations were not affected by thermal environment and were not related to ADG. Pituitary cells from H animals secreted and contained more PRL than cells from C animals (p < .05). Plasma PRL values were correlated with ADG (r = .54, p < .05), but did not differ between thermal groups. Stimulated in vitro PRL (TRH-vehicle) secretion was positively related with ADG only in the H group (r = .97, p < .001). In contrast, cellular PRL content decreased with ADG in cells from the H barrows (r = -.8, p < .05). Lactotroph function was not related to growth in cells from C pigs. In summary, 1) heat enhanced PRL secretion and cell content; 2) growth and somatotroph function were inversely related; and 3) serum PRL and the PRL response to TRH in cells from H barrows were positively related to growth.

Performance, carcass composition, and blood hormones and metabolites of finishing pigs treated with porcine somatotropin in hot and cold environments.

Two experiments were conducted to assess the ability for recombinant porcine somatotropin (rpST)-treated pigs to perform and cope with the demands of hot and cold environments. In the first experiment, finishing pigs were exposed to either a thermoneutral (TN; 18 to 21 degrees C) or a hot environment (H; 27 to 35 degrees C) for 35 d. In the second experiment, pigs were exposed to a TN or cold environment (C; 5 to 15 degrees C). The rpST delivered by a 6-wk prolonged-release system had no effect on ADG, whereas both H and C reduced ADG by 29.4 and 11.8%, respectively. In the first experiment, rpST-treated pigs consumed 17.6% less feed than control pigs, whereas rpST-treated pigs in H consumed 24.4% less feed than rpST-treated pigs in TN. Overall feed/gain ratios through the first 4 wk of both studies were improved by 21.8 and 14%, respectively, by rpST (P < .05) and were 24.3% poorer in C (P < .05) than in H. The changes in blood concentrations of pST, IGF-I, and IGF-II associated with rpST were not influenced by the different environments. Total body composition of rpST-treated pigs had increased amounts of protein (P < .05) and decreased amounts of fat (P < .05); H further reduced fat (P < .05). The C resulted in reduced protein content (P < .05). No evidence of thermal imbalance due to rpST was found as assessed by rectal temperature, respiration rate, and heat production estimated by indirect calorimetry and chemical analysis.

Evaluation of the mitogen-induced proliferation and cell surface differentiation antigens of lymphocytes from pigs 1 to 30 days of age.

A study was conducted to characterize aspects of the immune system in the pig from 1 to 30 d of age. Pigs were killed on d 1 (n = 6), d 18 or 19 (n = 6), and d 27 to 30 (n = 7) of age. Lymphocytes were isolated from the blood, thymus, and spleen. Lymphocyte function was assessed for ability to proliferate as induced by concanavalin A (Con A), phytohemagglutinin (PHA), and pokeweed mitogen (PWM). Cell surface differentiation antigens on the lymphocytes were evaluated for percentages of cells expressing CD2+, CD4+, CD8+, and SLA class II molecules. Responses of lymphocytes from blood, thymus, and spleen to any of the mitogens were relatively low d 1 through 16; the greatest proliferation occurred by d 28. No detectable percentages of the cell surface differentiation antigens were found on d 1 and changes varied with age and organ. The results indicate that the porcine immune system is not fully developed at birth and the expression of cell surface differentiation antigens seems to occur before the lymphocytes have the ability to respond to mitogens.

Effects of a porcine somatotropin implant on tissue mineral status of finishing pigs exposed to a thermoneutral or cold environment.

An experiment was conducted with 24 crossbred (Landrace x Yorkshire x Duroc) finishing pigs (mean BW 85 kg) to study the effects of a single 100-mg recombinant porcine somatotropin (rpST) implant on the tissue mineral status of pigs exposed to either a thermoneutral (TN; 18 to 21 degrees C, 50 to 55% RH) or cold (C; 5 to 15 degrees C, 50 to 70% RH) environment until BW averaged 110 kg. The implants used in this study delivered an average 2.4 to 2.5 mg of rpST/d during the course of the study. Control pigs were implanted with a placebo. All diets were supplemented with minerals at levels that either met or exceeded the requirements of an 85-kg pig. At slaughter (mean BW 110 kg), tissues were collected and analyzed for selected macro- and microminerals. Pigs treated with rpST had higher (P < .05) Ca concentrations and total Ca in liver and kidney and higher (P < .05) Ca concentrations in muscle. Total P, Mg, Na, and K were all higher (P < .05) in the liver and kidneys of rpST-treated pigs. In general, rpST had little influence on Cu, Zn, and Fe in tissues. No consistent trend was evident in the response of tissue minerals to environmental temperature. Results indicated that pigs treated with rpST and supplemented with adequate minerals accumulated more minerals in certain tissues than did pigs not given rpST.

Pemphigus vulgaris and vegetans.

Pemphigus vulgaris, which has multiple clinical variants, is an autoimmune blistering disorder of skin and mucous membranes, usually affecting the elderly, with a strong immunogenetic link. Immunologic studies of this disease have been productive in defining the pathophysiology of blister formation and the characteristics of the pemphigus antigen. New therapies resulting from the newest research techniques would prevent the global immunosuppression that occurs during drug therapy with systemic glucocorticoids, which is the cornerstone of therapy for patients afflicted with this potentially life-threatening disorder.

Effect of a hot environment on performance, carcass characteristics, and blood hormones and metabolites of pigs treated with porcine somatotropin.

A study was conducted to compare the effects of a single 100-mg recombinant porcine somatotropin (rpST) implant on performance, carcass characteristics, and blood hormones and metabolites of 40 finishing pigs exposed to either a thermoneutral (TN; 18 to 21 degrees C) or hot environment (H; 27 to 35 degrees C) for 28 or 35 d. Pigs in H gained at a slower rate (P less than .01) than pigs in TN. Control and rpST-treated pigs gained at similar rates in respective environments. The rpST-treated pigs consumed 13% less feed (P less than .01) than the control pigs in both environments, and pigs in H consumed 19% less feed (P less than .01) than pigs in TN. Feed efficiency for rpST-treated pigs was 15% better (P less than .01) than that for control pigs; environment had no effect on feed efficiency. When slaughtered, pigs treated with rpST had less (P less than .01) leaf fat and less (P less than .01) 10th rib backfat than control pigs. Pigs in H had a lower (P less than .01) final BW and less leaf fat and backfat than pigs in TN. The rpST and H had various effects on blood hormones and metabolites. The results demonstrated that the benefits of this form of rpST treatment achieved under TN were also achieved in H with no interactions between the hormone and environment.

Physiologic and immune responses associated with 48-hour fast of pigs.

We sought to determine the effect of 48 hours of fasting on physiologic and immune responses of pigs. Sixteen crossbred barrows, approximately 8 weeks of age, were housed in a controlled environment (21 degrees C, 45% RH) with feed and water ad libitum. After 10 days, eight pigs were fasted for 48 hours with water available ad libitum; the remaining eight received feed and water ad libitum. Blood samples were obtained by venipuncture before fasting, at the end of 48-hour fasting, and 3 and 10 days later. No significant differences in responses to mitogens PHA or Con A were noted in whole blood or isolated lymphocyte cultures. Changes in numbers of leukocytes, neutrophils, and serum cortisol concentrations, but not of lymphocytes, were significant. The results suggested that short-term fasting transiently reduces the number of neutrophils and increases serum cortisol concentrations, with no effect on blastogenic responses of lymphocytes to selected mitogens.