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Biomedical subjects

H Eiler

Publications and source records attributed to H Eiler.

At least 37 records · Page 2Linked to original sources
PubMed1986

Effect of plasma concentrations of ovarian steroids on their passage into uterine lumen in rabbits.

Significant increment of blood-borne ovarian steroids are found in the uterine lumen 1 h after mating. Is the transfer of ovarian steroids into the uterus determined by the peripheral blood concentrations of the ovarian steroids? To answer this question, rabbits, ovariectomized 24 h earlier, were infused over a 1-h period with either estradiol (E2; 0.7 and 7.0 micrograms/h), progesterone (P4; 74 and 740 micrograms/h), or testosterone (T; 0.45 and 4.5 micrograms/h). E2, P4, and T were determined in the tissue and flushings of the uterus and tissue and flushings of the esophagus and plasma. A different group of rabbits was infused with E2 (0.7 micrograms), P4 (74 micrograms), and T (0.45 microgram/h) combined. The increase in plasma steroid concentration after infusion of either E2, P4, or T was reflected in an elevation of these steroids in the uterine lumen, albeit not in the same ratios as found in plasma. The simultaneous infusion of E2, P4, and T blocked completely the passage of T and decreased (P less than 0.05) the passage of E2 into the lumen of the uterus. Treatments did not affect the steroid concentration in the wall of the uterus. It was concluded that the content of E2, P4, or T in the uterine flushing increased when E2, P4, or T was infused individually. However, when these steroids were infused together, there was selective inhibition of the transfer process.

Animals↗
PubMed1984

Stages of hyperadrenocorticism: response of hyperadrenocorticoid dogs to the combined dexamethasone suppression/ACTH stimulation test.

A study was designed to evaluate the response of blood cortisol content in dogs tentatively diagnosed as having hyperadrenocorticism by using the combined dexamethasone suppression/ACTH stimulation test procedure. Four groups of abnormal responses were identified in 54 dogs. In group I (14.8% of the dogs with abnormal responses), the only abnormality was partial suppression with dexamethasone (clinically normal dogs suppressed to less than 10 ng/ml). In group II (29.6%), 2 abnormalities were found: partial suppression with dexamethasone and hyperreactivity to the ACTH stimulation test. In group III (typical pituitary-dependent hypercortisolism, 48.1%), 3 abnormalities were found: base-line hypercortisolemia, partial suppression with dexamethasone, and hyperreactivity to the ACTH stimulation test. In group IV (7.4%), 2 abnormalities were found: base-line hypercortisolemia and partial suppression with dexamethasone. Base-line blood cortisol content was normal in 44.4% of the adrenopathic dogs. A normal response to ACTH stimulation was seen in 25.9% of the dogs, and 74.1% of the dogs hyperreacted to the ACTH stimulation test. All of the adrenopathic dogs were found to suppress partially with dexamethasone. Failure to suppress the adrenal gland completely (less than 10 ng/ml) with dexamethasone was the most consistent finding in adrenopathic dogs when using the combined dexamethasone suppression/ACTH stimulation test procedure. It was concluded that the test procedure is feasible, flexible, and convenient for clinical situations. Also, these results suggested that there may be several stages in the negative feedback failure associated with hyperadrenocorticism in dogs.

Adrenal Cortex Function Tests↗
PubMed1984

Uterotonic effect of prostaglandin F2 alpha and oxytocin on the postpartum cow.

Uterine motility was measured in 6 mixed-breed beef cows 48 to 72 hours after parturition, using an intrauterine balloon technique. Baseline uterine motility was measured for 30 minutes after a stabilization period. After 25 mg of prostaglandin F2 alpha (PGF2 alpha) was given IM, motility was recorded for 2 to 4 hours. After PGF2 alpha injection, 200 IU of oxytocin was given IM and motility was recorded for 2 to 4 hours. Twenty-four hours later, oxytocin treatment was administered, and 2 to 4 hours later, PGF2 alpha was given. The tension-time index was calculated. When PGF2 alpha was given initially, it did not affect (P greater than 0.05) uterine motility. However, oxytocin after PGF2 alpha increased uterine motility an average of about 225% of that of base line 20 minutes after injection. When oxytocin was given before PGF2 alpha treatment, the average increment of uterine motility was 875% above base line 20 minutes after oxytocin injection. The injection of PGF2 alpha did not affect uterine motility significantly (P greater than 0.05), whether given before or after oxytocin treatment. There was a linear decrease in the uterotonic effect of oxytocin between 10 minutes and 2 hours. When oxytocin was injected first, the correlation coefficient for the time-response relationship was -0.98. When oxytocin was injected after PGF2 alpha, the correlation coefficient was -0.84. Seemingly, PGF2 alpha should not be used as a uterotonic agent in the postpartum cow; however, oxytocin was an effective uterotonic agent.

Animals↗
PubMed1983

Retention of calcium in intestinal wall of the rabbit by treatment with a glucocorticoid.

In this work, consideration was given to the possibility that increased retention of Ca in the intestinal wall may have resulted in the glucocorticoid-treated animal. Rabbits were treated with pharmacological doses of either dexamethasone, estrogen, or progesterone during 1 wk. Two milliliters of solution containing Ca (plus Mg, K, and Na) were infused into a double-ligated (4 cm apart) gut loop (jejunum). In addition, an adjacent loop was double ligated but received no infusion. Uterine horns were treated in the same way as the gut and were used as controls to test for organ specificity. After the organs were infused with the calcium solution, they were returned into the abdominal cavity for a 4-h period. Dexamethasone treatment was given to a different group of rabbits in which neither surgery was performed nor mineral solution was infused into the lumen of the intestine; in this experiment calcium concentrations were measured in the mucosa, submucosa, and serosa layer obtained from the duodenum, midjejunum, and distal jejunum. In rabbits subjected to surgery, the concentration of Ca in the whole wall of the intestine of the dexamethasone-treated rabbits (45.4 +/- 2.6 mM/kg dry tissue) was twice as large as in controls (22.6 +/- 3.2 mM/kg dry tissue) (P less than 0.05). Mg concentrations were moderately (17%) increased (P less than 0.05). In the group of rabbits receiving dexamethasone but not subjected to surgery, the concentration of Ca in the duodenum (mucosa, submucosa, and whole wall), midjejunum (whole wall), and distal jejunum (submucosa) was significantly (P less than 0.05) elevated as compared with controls. In these rabbits, the duodenum was the most affected segment of the intestine. The effect of dexamethasone was both organ and steroid specific but not mineral specific. This result suggests that one of the effects of the glucocorticoid (dexamethasone) treatment on the intestinal wall was to increase the retention of Ca.

Animals↗
PubMed1981

Internal vomiting in the ruminant: effect of apomorphine on ruminal pH in sheep.

Five sheep, with a rumen fistula inserted, were each injected (IV) with apomorphine (18 mg) and ruminal pH was measured every 5 minutes during a 1-hour period. During the base-line period (30 minutes) that preceded apomorphine injection, pH was constant in individual sheep and te group mean (+/- SD) was 7.1 +/- 0.35. After apomorphine was injected, group mean was 6.9, 6.0, 6.3, 6.3, 6.3, 6.4, 6.4, 6.5, 6.7, 6.9, 6.9, and 7.1 at 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, and 60 minutes, respectively. The pH reduction of ruminal content was recorded in 4 of the sheep. Maximal reduction occurred in the 10-minute period after apomorphine was injected. The pH returned to control value within 40 to 50 minutes after injection. Vomitus was not expelled through the mouth by any of the sheep. It was concluded that expulsion of acidic abomasal contents back into the preabomasal compartment (internal vomiting) was the cause of acidification of the rumen after apomorphine was injected.

Animals↗
PubMed1981

Refractoriness of both uterus and mammary gland of the cow to prostaglandin F2 alpha administration:P clinical application.

Uterine and mammary pressure changes were simultaneously measured in lactating nonpregnant cows injected (IV) with different doses (0.1 to 32.0 mg) of prostaglandin F2 alpha (PGF2 alpha). The total work of the uterus increased up to 250% of base-line value as the dose of PGF2 alpha was increased. But, a dose-response relationship was not seen in the uterus. Partial refractoriness was developed in the uterus, and total refractoriness was developed in the mammary gland. Further challenge with oxytocin (30 U) elicited significant responses in both the uterus and the mammary gland. Because of the development of refractoriness and side effects, PGF2 alpha is not recommended as a drug to be used when mechanical evacuation (free of endocrine effect) of the uterus or mammary gland (or both) is indicated.

Animals↗
PubMed1981

Inhibition of gastric hydrochloric acid secretions in the rat given Ostertagia ostertagi (a gastric parasite of cattle) extract.

The immersion of freshly collected Ostertagia ostertagi adults into saline solution (NaCl, 0.9%; pH 1.0) resulted in 100% mortality of worms within a 10-minute period. At pH 7.0, mortality was 58% after 270 minutes. At pH 2.2, which approximates the usual abomasal pH, 100% mortality resulted within 60 minutes. In the stomach of rats injected with an extract of O ostertagi (from the abomasum of cattle), there were decreased total secretion of hydrogen ions and volume of secretion (P less than 0.05) and increased mean pH of gastric secretion (P less than 0.05). These effects were similar to those found in stomach of rats treated with cimetidine. Results indicated that the pH of the abomasum was detrimental to parasitic survival and that hypochlorhydria found during ostertagiosis may be mediated partially by a chemical released from the parasite.

Animals↗
PubMed1980

Distribution of adrenergic receptors in the domestic fowl oviduct.

The effect of epinephrine, phenoxybenzamine (alpha-receptor blocker), and propranolol (beta-receptor blocker) on the oviductal motility in an in vitro system was investigated in strips from infundibulum, magnum, isthmus, and uterus from laying hens. Epinephrine resulted in a significant (P less than .05) contraction of both infundibulum (+166.6%) and magnum (+70.3%) and relaxation of the uterus (-56.9%), while the response of the isthmus was inconsistent. Epinephrine induced contractions in propranolol blocked strips in all four oviductal segments studied (infundibulum, +138.1; magnum, +70.4; isthmus, +35.9; and uterus, +30.1%). Epinephrine, in phenoxybenzamine-blocked strips, resulted in relaxation of all segments (infundibulum, -27.5; magnum, -40.5; isthmus, -63.4; and uterus -53.6%). These results suggest that the activity of alpha-excitatory adrenergic receptors is greater in the anterior than in the posterior segment of the oviduct. conversely, greater activity of beta-inhibitory receptors seems to be present in the posterior than in the anterior segment of the oviduct.

Adrenergic beta-Antagonists↗
PubMed1980

Combined dexamethasone suppression and cosyntropin (synthetic ACTH) stimulation test in the dog: new approach to testing of adrenal gland function.

A combined dexamethasone suppression and cosyntropin (synthetic ACTH) stimulation test was developed in the dog so that information concerning pituitary gland (hypophysis) and adrenal gland competence could be provided in a single trial, during a short time span. Treatment of dogs with dexamethasone (0.1 mg/kg, IM) resulted in total suppression (below assay sensitivity or < 10 ng/ml) of plasma hydrocortisone (cortisol) at postinjection hour (PIH) 2 in 100% of the dogs, whereas suppression was inconsistent at PIH 1. Cosyntropin (0.5 U/kg, IV) administration to normal or dexamethasone-suppressed dogs increased plasma hydrocortisone concentration 3.5 to 4.5 times base-line values at PIH 1, which was the time of maximal effect. The combined test concept for adrenal gland function is valid, convenient (three sample collections; 3-hour period), and allows testing of adrenal gland response to dexamethasone suppression and ACTH stimulation in a single trial. The following test procedure for dogs is recommended: (i) collect base-line plasma sample (0900 hours) followed by injection of dexamethasone (0.1 mg/kg, IM); (ii) collect second plasma sample 2 hours after dexamethasone (to evaluate suppression of plasma hydrocortisone concentration) followed by the injection of cosyntropin (0.5 U/kg, IV); and (iii) collect a third plasma sample 1 hour later to evaluate plasma hydrocortisone concentration after cosyntropin stimulation.

Adrenal Glands↗
PubMed1979

Adrenal gland function in the horse: effects of cosyntropin (synthetic) and corticotropin (natural) stimulation.

The plasma concentration of hydrocortisone was determined in mares given either cosyntropin (100 IU, given IV) or corticotropin (200 IU, given IM). Plasma hydrocortisone concentrations of the mares treated with cosyntropin increased by 46%, 57% and 80% at 30, 60, and 120 minutes, respectively, when compared with base-line values; these values returned to base line at 240 minutes. In mares treated with corticotropin, mean plasma hydrocortisone concentrations increased by 42%, 143%, 101% and 155% at 30, 60, 120, and 240 minutes, respectively, when compared with base-line values. Differences in total leukocyte count, total eosinophil count, and plasma concentrations of electrolytes (calcium, sodium, magnesium, potassium) of cosyntropin- and corticotropin-treated mares, and these values in control animals were not significant. Results of the present study indicated that the horse responds to small dosages of cosyntropin (IV) in a prompt and reproducible manner as determined by plasma hydrocortisone values. Response to corticotropin was slow and less consistent. Thus, administration of cosyntropin to the horse, according to test results with paired samples collected (before administration and again at 2 hours after injection), was found to be a prompt and meaningful test of adrenal gland function.

Adrenal Glands↗
PubMed1979

Induction of intestinal evacuation or vomition (or both) in the dog by prostaglandin F2alpha injection: clinical potential.

Different groups of dogs were given prostaglandin F2alpha IM. The dosage range was between 0.022 and 0.555 mg/kg of body weight. Defecation, including contents from the cranial portion of the large intestine, occurred in 40% to 100% of the dogs within 3.16 to 12.5 minutes after injection depending on dosage administered. Defecation (83.3% of dogs), without vomition, occurred in dogs given a dosage of 0.111 mg/kg. Emesis (87.5% of dogs) and defecation (75.0% of dogs) were observed in dogs given a dosage of greater than or equal to 0.444 mg/kg. Emesis occurred in 1.6 to 2.6 minutes after defecation in dogs given more than 0.444 mg/kg. Latency for emesis response varied between 3.2 and 11.5 minutes. The effect of the drug lasted approximately 15 minutes, with most dogs showing a single episode of defecation or vomition (or both). Besides a marked increase in respiratory rate, side effects were minor. Seemingly, prostaglandin-F2alpha may become the preferred drug for the clinical inducement of vomition and defecation in dogs.

Animals↗
PubMed1979

Mastitis-metritis-agalactia complex in sows: effect of the dosage of oxytocin on intramammary pressure in lactating healthy sows.

The dose-response and time-response relationships between injected oxytocin and intramammary pressure were investigated in normal lactating sows. In less than 39 s after 20, 40, or 80 U of oxytocin was given (IM injection), there was a rapid initial increase in intramammary pressure (15 to 27 mm of Hg) which lasted 22 to 32 s. After this initial response, there were secondary oscillations in pressure which lasted approximately 40 minutes (20 U) and up to 60 minutes (40 or 80 U). Changes in intramammary pressure during each oscillation varied between 1 and 5 mm of Hg. Mean values for frequency and amplitude of oscillations and total work (area under the trace) were measured. Compared with response obtained after 20 U of oxytocin was given, responses obtained at the 40-U or 80-U dose level had an increased frequency (150.0% and 249.0%, respectively) and total work (36.6% and 104.4%, respectively), but not amplitude. Thus, there may be some clinical advantage in milk let-down effect when sows are given the larger doses of oxytocin (40 or 80 U). These results indicate that newborn pigs should be allowed to nurse at the same time in which oxytocin is injected.

Animals↗
PubMed1979

Porcine mastitis-metritis-agalactia (MMA) syndrome: mammary gland responsiveness to oxytocin given to healthy sows during lactation.

Mammary gland responsiveness to exogenous oxytocin during lactation was assessed by measuring changes in intramammary pressure of healthy sows given (IM injection) synthetic oxytocin (40 U). Response to oxytocin was measured once a week for the first 8 weeks of lactation. Recordings of pressure changes were expressed as mean area (cm2) under the trace at each 10-minute interval over 30 minutes after oxytocin had been given. During the 2nd week of lactation, there was a 55.3% increase (P less than 0.05) in responsiveness to oxytocin (25.1 +/- 4.2 cm2/10 minutes) as compared with the 1st week (13.9 +/- 2.2 cm2/10 minutes). Responsiveness decreased, however, from the 2nd to the 8th week. Since the incidence of mastitis-metritis-agalactia in sows is particularly high during the 1st week of lactation, low responsiveness of the mammary gland to oxytocin may be a contributing factor.

Animals↗
PubMed1978

Effect of luteinizing hormone on ovarian release of steroids: ovarian vein-sampling technique in conscious gilt.

After ventral midline laparotomy was done, silastic tubing was inserted into the ovarian vein through a cranial branch of the uterine vein. The free end of the silastic tubing was exteriorized through a perforation of the dorsal wall of the vagina and then passed to the outside of the vulva. The free end of the tubing was sutured to the skin approximately 3 cm lateral to the ventral aspect of the vulva. In the ovarian vein of the sow, the plasma concentration of ovarian steroids was 1.5 to 4.0 times greater than that in peripheral blood, thus making possible the detection of changes not found in peripheral plasma samples. Blood samples were taken immediately after surgical placement of the sample collection tube for a 4-month period from unstressed gilts. Surgical stress seems to increase significantly the release of steroids into the ovarian vein. After the luteinizing hormone injection, progestin but not estrogen was consistently released into the ovarian vein.

Animals↗