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Biomedical subjects

L M Harrison

Publications and source records attributed to L M Harrison.

At least 73 records · Page 4Linked to original sources
PubMed1988

Comparison of hypothalamus-pituitary-adrenal axis suppression from superpotent topical steroids by standard endocrine function testing and gas chromatographic mass spectrometry.

We evaluated 38 males who had psoriasis vulgaris for evidence of hypothalamus-pituitary-adrenal axis suppression (HPAS) during treatment with superpotent topical glucocorticosteroids. All men were treated with 49 g per week of either Betamethasone Diproprionate in an optimized vehicle or Clobetasol Proprionate ointment. Three methods used to assess HPAS were compared. Classic 8 a.m. plasma cortisol measurements, urinary-free cortisol, and 17-hydroxycorticosteroid determinations and gas chromatograph-mass spectrometry (GCMS) quantitation of urinary cortisol metabolites were compared. Values for all methods were obtained just prior to therapy and at days 4, 7, 14, and 21 during therapy and at day 28 after treatment was stopped for 7 d. Plasma cortisol measurements correlated well with other measures of HPAS. GCMS determination of urinary cortisol metabolites was slightly more sensitive at detecting HPAS than the other two methods. Persistent HPAS after day 7 was only appreciated by GCMS. Urinary-free cortisol and 17-hydroxycortisol was the least sensitive of the three methods. Analysis of urinary cortisol metabolites by GCMS may be most useful in the monitoring of HPAS resulting from use of topical glucocorticosteroid preparations.

17-Hydroxycorticosteroids↗
PubMed1987

Progesterone production, LH receptors, and oxytocin secretion by ovine luteal cell types on days 6, 10 and 15 of the oestrous cycle and day 25 of pregnancy.

Corpora lutea were collected from sheep on Days 6, 10, and 15 of the oestrous cycle and Day 25 of pregnancy and dissociated into single cell suspensions. Purified preparations of large and small luteal cells were prepared by elutriation on all days except Day 6. Basal progesterone production by large cells was 6-8-fold higher than by small cells (36-65 vs 6-9 fg/cell/min). Oxytocin secretion was maximal on Day 6 (1.0 fg/cell/min) and declined thereafter. The number of receptors for LH increased between Day 6 and Day 10 and the two cell types had an equal number of receptors on Days 10 and 15 (19,000-23,000). Large cells on Day 25 of pregnancy had fewer receptors (12,000) than did small cells (26,000). Progesterone secretion by small luteal cells from all days examined was stimulated by LH (0.01-1000 ng/ml) in a dose-dependent manner; maximum sensitivity to LH occurred on Day 10. Despite the presence of receptors for LH on large cells, LH failed to stimulate progesterone production. Basal production of progesterone by large and small cells, and the response of small cells to LH, was not influenced by day examined. Re-combinations of large and small cells from Day 10 synergized to increase progesterone secretion. Prostaglandin E-2 (0.1-1000 ng/ml) did not stimulate progesterone secretion by large or small cells.

Animals↗
PubMed1986

Influence of insulin and energy intake on ovulation rate, luteinizing hormone and progesterone in beef heifers.

Ovarian and gonadotropin responses to insulin and energy restriction were investigated in a 2 X 2 factorial experiment using 2-yr-old Brangus heifers. Thirty heifers were paired by weight and body condition, then assigned to treatment groups receiving 75 (LE) or 180% (HE) of NRC recommendations for dietary energy for maintenance. Diets were adjusted weekly to maintain daily .25 to .5 kg weight loss or 0 to .25 kg weight gain, respectively. On d 10 of the first estrous cycle subsequent to the initial 45 d of feeding, heifers within each dietary group were allocated to receive twice daily infusions of either 40 U insulin (I) or saline (C). Infusions began at 5 and 10 h postprandial and were given in six boluses, 20 min apart. Infusions continued daily until d 20 or estrus, whichever occurred first. On d 11, blood samples were collected at 15-min intervals for 12 h to determine luteinizing hormone (LH) and insulin concentrations. On d 16 to 20, twice daily im injections of 1 mg follicle stimulating hormone (FSH) were administered. Heifers were ovariectomized on d 11 after estrus. Number of corpora lutea (CL) in LE-I heifers was greater (P less than .05) in LE-C, HE-C or HE-I. Total CL weight (g) per heifer was greater (P less than .05) in HE-C and LE-I heifers than in LE-C. Individual CL wt was heavier in HE than in LE heifers (P less than .05).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1985

Cloprostenol inouced luteal regression in the beef cow. I. Ovarian response and endocrine changes.

Forty-two cycling, multiparous beef cows (percentage-Brahman) were given two injections of 500 ug Cloprostenol (CLP) 11 days apart. Cows were randomly allocated to be ovariectomized at 0, 12, 24, 36, 48, 60 or 72 hr after the second CLP injection. Mean CL weight declined within 36 hr after CLP. Mean concentration of P4 in luteal tissue increased between o and 60 hr, while mean P4 content per CL declined by 12 hr after CLP. There was a precipitous decrease in mean serum P4 by 12 hr following CLP injection. Serum E2 was elevated until 24 hr and then declined through 72 hr after CLP. Follicular T concentration increased from 0 to 48 hr and then decreased by 60 hr. We conclude that CLP caused rapid diminution of luteal function which was accompanied by a reduction in P4 content but not in P4 concentration. Futhermore, the concentration of E2 in large follicles decreased by 72 hr post-CLP which is consistent with an alteration of the steroidogenic pathway in the periovulatory follicle.

Journal Article↗
PubMed1985

Cloprostenol induced luteal regression in the beef cow. II. Histological evaluation of corpora lutea and correlation with luteal progesterone.

Forty-two cycling, multiparous beef cows (percentage-Brahman) were injected twice at 11-d intervals with 500mug Cloprostenol (a prostaglandin F(2alpha) analog) to induce luteolysis. Cows were randomly assigned for ovariectomy at 12 hr intervals from 0 to 72 hr post-injection. Corpora lutea were excised and one-half of the corpus luteum was stored in phosphate-buffered formalin until mounting and staining with hematoxylin and eosin. The other half of the CL was snap-frozen for determination of progesterone content and concentration. Luteal cell density increased following Cloprostenol injection and was significantly correlated with a shift from predominantly healthy Type I cells to predominantly degenerating Types III and V cells. Cell mitosis tended to decrease by 12 hr and was lower by 24 hr post-injection. Cell pyknosis increased by 24 hr post-injection and was correlated with the decrease in percentage of healthy luteal cells. No pattern was detectable in cell karyorrhexis. Histological regression of the CL was inversely correlated with CL progesterone content. Therefore, we conclude that a reduction in cell mitosis is the earliest morphological sign of degeneration of the CL and that the CL follows a well-defined sequence of regression which is accompanied by a decrease in progesterone content.

Journal Article↗
PubMed1984

Treatment of ectopically erupting permanent molars.

Eruption of a first permanent molar ectopically is a common occurrence in any office in which a significant number of children are treated. Approximately 65 per cent of the ectopically erupting molars will self-correct. It is imperative that the dentist closely examine all preschool children to determine the possibility that the condition will occur and follow the child closely to determine the subsequent need for treatment. If clinical treatment is advisable the dentist can use a modified version of the Humphrey appliance to successfully and rapidly correct ectopically erupting molars with relative ease.

Child↗
PubMed1982

Evidence for seasonal and nutritional modification of ovarian and pituitary function in crossbred heifers and Brahman cows.

Alterations in endocrine response in the bovine female after consumption of monensin or exposure to changes in season were observed in two experiments. Thirty-three monensin-fed (M) or control (C) crossbred heifers in Exp. 1A were given a porcine follicle stimulating hormone (FSH-P) challenge on d 16 to 21 postestrus. Nine M heifers ovariectomized (OVX) on d 11 after the FSH-challenged estrus had a greater number of smaller corpora lutea (CL; P less than .005) than did nine d 11 OVX C heifers. Serum progesterone (P4) concentrations were greater in M on d 5 through 13 following the FSH-challenged estrus (P less than .001). Seven M and seven C Brahman cows in Exp. 1B given an identical FSH challenge had similar increases in CL number and size. In Exp. 2, blood samples were obtained from 14 M and 13 C Brahman cows during winter (WI), early spring (ESp) and late spring (LSp) to characterize the preovulatory LH surge. During each seasonal period, blood samples were taken hourly from estrus through 24 h postestrus for each cow. Only one of five WI-C cows had a preovulatory LH surge compared to five of five WI-M cows (P less than .01). No differences were found in the number of cows having an LH surge in ESp or LSp groups. Analysis of combined WI and ESp group values indicated a difference in timing of the LH surge by M or C treatment. Of those cows that had an LH surge, only three of 10 C had peak LH values later than the first sample taken, compared with 10 of 15 M (P less than .10). A heightened LH response was detected in M cows in all comparisons of LH surge profiles (P less than .005). Concurrent with changes in season from WI to ESp was an increase in number of C cows having an LH surge (one of five vs nine of 10; P less than .005), and elevated LH values in ESp-C and M groups compared with WI-C and M groups (P less than .05). Midluteal blood samples taken after every estrus indicated P4 to be greatest in February M cows (P less than .10) and P4 tended to be greater in February and lower in January for all groups. Conclusions are that monensin affects the FSH-P-induced ovulation rate of bovine females of all ages. Seasonal effects occurring between the shortest and longest days of the year exert their greatest influence on the preovulatory LH surge and P4 concentrations in Brahman cows between January and March. Seasonal effects appear to be partially modulated by nutritional factors.

Animals↗
PubMed1981

Serum luteinizing hormone levels in Brangus cows following variable suckling intensity and administration of various levels of estrogen.

Fifty Brangus cows were randomly allotted to suckled (S) or nonsuckled (NS) treatment groups on day 20 postpartum. Suckled cows were nursed at 6 hr intervals for 72 hours. Nonsuckled cows were separated from their calves for the entire 72 hours. At 24 hr after initial separation from calves, S and NS cows were given an I.M. challenge of 0, 0.5, 1.0, 2.0 or 4.0 mg estradiol-17beta (E2) to induce a luteinizing hormone (LH) surge (five cows per treatment group). Blood samples were taken at the time of E2 injection and at 2 hr intervals until hr 48 post-injection. Blood serum was analyzed for LH content via radioimmunoassay. Suckled and NS cows manifesting an LH surge after receiving less than 4 mg E2 were 2 of 15 vs 9 of 15 (P<.01), or 4 mg E2 dose were 5 of 5 vs 5 of 5, respectively. Greater serum LH concentrations in NS than S cows were found with dose levels of 0, 0.5 and 1.0 mg E2 (P<.005), but there was no difference by period. Differences by treatment (P<.05) and by period (P<.005) were found at the 2 mg E2 dose. Suckled and NS cows having an LH surge at less than a 4 mg E2 challenge had no differences in LH concentration or timing parameters. Four mg E2 hastened the time of onset of the LH surge (P<.025), time till peak height of the surge (P<.025) and completion of the surge (P<.10). No differences in postpartum interval or conception rate were found between S and nonsuckled. Suckling impairs hypothalamic/pituitary response to low E2 challenge dose and elicits changes in timing parameters in response to high E2 dosage.

Journal Article↗
PubMed1975

Analysis of activity of muscle spindles of the jaw-closing muscles during normal movements in the cat.

Recordings have been made of afferent activity from spindles of the jaw-closing muscles, together with jaw movement and e.m.g. from temporalis and masseter in conscious, unrestrained cats. 2. In the twenty-nine units studied, the pattern of spindle behaviour observed during eating and lapping was generally what might be expected of stretch receptors. Maximal firing frequencies were found during opening of the mouth (lengthening), while during active closing the discharge was progressively reduced or abolished. Nevertheless, changes in the relation of stretch to firing frequency in different movements indicated that fusimotor drive was not constant. 3. spindle afferents could be divided into two groups on the basis of their maximal firing frequency during eating. "High-frequency" units (range 240-600 impulses/sec) showed pronounced velocity sensitivity, which supports the proposal that they correspond to spindle primaries. 'Low-frequency" units (range 80-200 impulses/sec) showed predominantly length sensitivity and probably correspond to secondary endings. 4. Length sensitivity of low-frequency units was considerably greater in lapping movements than in eating, indicating increased static fusimotor drive in the former. Sensitivity in the opening phase of eating was indistinguishable from that recorded in deeply anaesthetized animals. 5. High-frequency units were generally silenced immediately active shortening commenced. 6. No simple relationship existed between temporalis or masseter e.m.g. and spindle firing. 7. These results imply that normal masticatory movements are not initiated or driven to any appreciable extent via the fusimotor route. Close alpha-gamma co-activation is not a feature of this situation. On the other hand, in some other movements, such as licking the lips, fusimotor drive could fluctuate so as largely to cancel the unloading effects of active muscle shortening.

Action Potentials↗