Search PubMed⌕ Search

Biomedical subjects

J J Wagner

Publications and source records attributed to J J Wagner.

25 records · Page 2Linked to original sources
PubMed1991

Endogenous opioids released from perforant path modulate norepinephrine actions and inhibitory postsynaptic potentials in guinea pig CA3 pyramidal cells.

The stimulus parameters needed for the release of endogenous opioid peptides were investigated using an in vitro radioligand displacement assay in living guinea pig hippocampal slices. Electrical stimulation of the enkephalin-containing fibers in the perforant path caused the release of endogenous opioid peptides and the subsequent displacement of [3H]-[D-Ala2,N-methyl-Phe4,glyol5]enkephalin binding. High frequency trains of stimuli (10 Hz for 1 sec every 10 sec) were more effective than lower frequency stimulation (1 Hz continuous) at evoking opioid peptide release. Having identified an effective stimulation paradigm able to release endogenous opioids, the electrophysiological effects of endogenous opioids on CA3 pyramidal cells were measured in the guinea pig hippocampal slice preparation. Unlike exogenously applied opioids, stimulated release of endogenous opioid peptides from the perforant path did not significantly reduce inhibitory postsynaptic potential (IPSP) amplitudes recorded in CA3 pyramidal cells. However, perforant path stimulation in the presence of naloxone did cause a dramatic increase in IPSP amplitudes. CA3 pyramidal cells were not directly affected by perforant path stimulation. The naloxone-sensitive increase in IPSPs was delayed 3 min in onset and lasted for several minutes. In addition, the increase in the IPSPs was specifically blocked either by the beta adrenergic antagonist propranolol or by pretreating the animals with reserpine. These findings indicate that endogenous opioids regulate the effects of norepinephrine in the CA3 region of the guinea pig hippocampus. In addition, endogenously released norepinephrine appeared to act on GABAergic interneurons to increase the amplitude of the IPSP recorded in CA3 pyramidal cells.

Animals↗
PubMed1991

Focal stimulation of the mossy fibers releases endogenous dynorphins that bind kappa 1-opioid receptors in guinea pig hippocampus.

Physiological release of endogenous opioids in guinea pig hippocampal slices was detected in an in vitro competition binding assay using [3H]U69,593, a kappa 1-selective radioligand. Veratridine-induced opioid release caused a decrease in [3H]U69,593 binding that was blocked by either tetrodotoxin addition or the removal of calcium from the incubation buffer. Focal electrical stimulation of opioid peptide-containing afferent pathways resulted in a decrease in [3H]U69,593 binding, whereas stimulation of a major afferent lacking endogenous opioid immunoreactivity had no effect. The addition of 6-cyano-7-nitroquinoxaline-2,3-dione blocked the reduction in [3H]U69,593 binding caused by perforant path stimulation, but not the reduction caused by mossy fiber stimulation, suggesting that the primary source of endogenous kappa ligands was likely to be the dentate granule cells. Antisera against dynorphin A(1-8) or dynorphin B peptides inhibited the effects of mossy fiber stimulation in the [3H]U69,593 displacement assay. Antisera against other prodynorphin- and proenkephalin-derived opioid peptides had no effect. As shown by receptor autoradiography, the distribution of kappa 1 binding sites was limited to the molecular layer of the dentate gyrus and the presubiculum region of temporal hippocampal slices. These results indicate that prodynorphin-derived opioids released under physiological conditions from the mossy fibers act at kappa 1 receptors in the guinea pig dentate gyrus.

6-Cyano-7-nitroquinoxaline-2,3-dione↗
PubMed1991

Influence of nutrition and body condition on pituitary, ovarian, and thyroid function of nonlactating beef cows.

Nonpregnant Hereford cows (n = 70) were used to determine the effect of nutrient intake and body condition on reproductive and thyroid function. Body condition scores (BCS; 1 = emaciated; 9 = obese) of cows averaged 5.0 +/- .2 on July 1, and cows were fed for 4 mo either to lose weight and BCS (thin; n = 22), to maintain weight and BCS (moderate; n = 24), or to gain weight and BCS (fat; n = 24). After November 1, cows received a complete ration to maintain weight and BCS. Cows were slaughtered in December (six thin, eight moderate, and eight fat cows) or the subsequent March (16 cows per group). Before slaughter, cows were given two injections of prostaglandin F2 alpha (PGF) 11 d apart. Six days after the second PGF injection, cows were simultaneously treated with 100 micrograms of gonadotropin releasing hormone (GnRH; i.m.) and 100 micrograms of thyrotropin releasing hormone (TRH; i.v.) and serum samples were obtained. The BCS of cows at slaughter (8 d after PGF) averaged 3.4, 5.3, and 7.1 (P less than .01) and carcass energy content averaged 243, 432, and 714 Mcal (P less than .01) for thin, moderate, and fat cows, respectively. Wet ovarian (P less than .001) and corpora lutea (P less than .01) weights were heavier for fat cows. Content of LH in the pituitary gland and concentrations of thyroxine (T4) in serum after GnRH/TRH were not influenced by nutrient intake or BCS. However, thin cows had greater concentrations (P less than .05) of LH in serum after GnRH/TRH than did moderate or fat cows. We conclude that nutrient intake and body energy reserves of beef cows influenced ovarian function and LH in serum after treatment with GnRH.

Animal Nutritional Physiological Phenomena↗
PubMed1990

Stimulation of endogenous opioid release displaces mu receptor binding in rat hippocampus.

Physiological release of endogenous opioids in the rat hippocampus was detected by an in vitro radioligand displacement assay using [3H][D-Ala2,N-methyl-Phe4,glyol5]enkephalin ([3H]DAGO), a mu selective opioid agonist. In this assay, radioligand binding to opioid receptors in the in vitro hippocampal slice was reduced by competition with endogenous opioids released following tissue depolarization. Veratridine-induced opioid release caused displacement of [3H]DAGO that could be blocked by either tetrodotoxin addition or calcium removal from the incubation buffer. Maximal displacement of [3H]DAGO also required the presence of peptidase inhibitors in the incubation buffer. None of the buffer composition changes directly affected [3H]DAGO binding to rat brain membranes. Calcium-dependent displacement of [3H]DAGO binding from mu receptor sites elicited by focal electrical stimulation depended on the intensity and frequency of stimulation and positioning of the electrode in the slice. Maximal displacement of [3H]DAGO binding was observed following high intensity (150-300 microA), high frequency (10-50 Hz) stimulation of the perforant path, a major afferent fiber system to the hippocampus previously shown to contain proenkephalin-derived opioids. Low frequency stimulation (0.1-1 Hz) was ineffective. Stimulation of the mossy fibers (containing both dynorphins and enkephalins) also significantly reduced mu receptor binding, but to a lesser extent. Electrical stimulation of the hippocampal slice at sites not containing opioid peptides did not cause mu receptor displacement. These results demonstrate that under physiological conditions, the release of endogenous opioids from the major opioid containing pathways can be detected in a single hippocampal slice following high frequency stimulation.

Animals↗
PubMed1988

Carcass composition in mature Hereford cows: estimation and effect on daily metabolizable energy requirement during winter.

Seventy-two mature, nonpregnant, nonlactating Hereford cows (400 kg) were utilized in a comparative slaughter trial to investigate the effects of carcass composition on the metabolizable energy (ME) required for maintenance in winter. Body condition score (CS), live weight (LW) and weight:height ratio (WTHT) were evaluated and compared as estimators of carcass composition in cows. Cows ranged in LW, CS and WTHT from 275 to 595 kg, 2.0 to 8.0 units and 2.29 to 4.62 kg/cm, respectively. Live weight, CS and WTHT predicted total carcass energy (TMCAL, r2 = .81, .85 and .83), carcass fat (FAT, r2 = .78, .82 and .80), carcass protein (PRO, r2 = .71, .74 and .70) and carcass water (WAT, r2 = .78, .71 and .77) with similar accuracy. When composition was expressed on a per unit weight basis, CS was superior to LW and WTHT as predictors of TMCAL/hot carcass weight, TMCAL/LW and FAT/hot carcass weight (r2 = .82, .60 and .64; .83, .58 and .62; and .82, .64 and .68, respectively). Forty-seven cows were individually fed a complete diet (2.50 Mcal ME/dry matter) in drylot for 114 d in yr 1 and 115 d in yr 2. Daily feed intakes were adjusted each week to maintain constant LW throughout the winter. Data were analyzed by fitting the model: ME intake = k-1 (carcass energy change) + f(CS)LW.75, where k = efficiency of ME use for carcass energy change and f(CS) = function of CS. Year as a class variable and the expression .1028 + .0234(CS) - .0025(CS)2 accounted for 41% of the variation in Mcal ME for maintenance/LW.75. Condition score was more closely related to carcass composition in mature cows than was LW or WTHT and cows in either a thin (CS = 3) condition or a fat (CS = 7) condition required less (4.4% and 8.9%) Mcal ME/LW.75 for maintenance than cows in moderate (CS = 5) condition.

Animals↗
PubMed1986

Postpartum weight and body condition loss and performance of fall-calving cows.

A total of 166 mature fall-calving Hereford cows were used to study the effects of weight and body condition losses on the reproduction of cows and on the performance of their calves. This study was conducted before and during the breeding season over a 3-yr period. The cows calved in a good body condition and were assigned to one of the following treatment groups: the MM group to maintain weight from calving (September - October) through breeding (December - January), the LM group to lose up to 10% of the postpartum weight from calving to the beginning of breeding and to maintain the weight during breeding, and the ML group to maintain weitht from calving to the beginning of breeding and to lose 10 - 15% of the postpartum weight during breeding. Weight losses were adjusted by altering daily amounts of protein supplement and forage. Cows in the LM treatment group lost 3, 17 and 6% of their postpartum weight before breeding in yr 1, 2, and 3, respectively, and they had a 10-d longer (P <0.05) interval from calving to first estrus than MM or ML group cows. The percentage of cows with ovarian activity at the beginning of breeding was reduced (37 vs 64%, P <0.01) for LM compared with MM cows. Treatment-by-year interactions were significant for pregnancy rate and ovarian activity at the end of breeding. In Year1, ML cows lost 14% of postpartum weight during breeding and had reduced (P <0.01) pregnancy rates compared with MM or LM cows (50 vs 79 and 88%). Only 41% of ML cows in Year 1 had luteal activity after estrus compared to 93% for MM and 79% for LM cows. During Year 2, LM cows lost 17% of postpartum weight before breeding, while ML cows lost 6% of their postpartum weight before breeding and 11% during breeding. Pregnancy rates tended to be reduced for both LM and ML cows compared to MM cows (53 and 65 vs 87%, P >0.10). The percentage of cows with ovarian activity at the end of breeding was reduced (P <0.05 for the LM treatment group and tended (P >0.10) to be lower for ML than for MM cows. In Year 3, pregnancy rates were greater (89, 84 and 85% for MM, LM and MM, respectively) for all groups. However, the percentage of cows with luteal activity after estrus was greater (P <0.05 for MM (94%) than for LM and ML (64 and 67%). Calf weaning weights (205 d in April) were not significantly influenced by treatment. We conclude that even if cows have adequate energy reserves at calving (good body condition), optimal reproductive efficiency of fall-calving range cows cannot be ensured.

Journal Article↗