Alicja Skupny
Harvard University
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Featured researches published by Alicja Skupny.
Psychopharmacology | 1988
Jack H. Mendelson; Scott E. Lukas; Nancy K. Mello; Amass L; James Ellingboe; Alicja Skupny
Acute administration of alcohol (0.695 g/kg) to healthy adult women resulted in peak blood alcohol levels between 70 and 75 mg/dl within 50–60 min after initiation of drinking. Alcohol induced a significant increase (x=18 pg/ml) in plasma estradiol levels (P<0.01). In contrast, after placebo ingestion, plasma estradiol levels did not change significantly. After alcohol intake, plasma estradiol levels reached peak values at 25 min following initiation of drinking when blood alcohol levels averaged 34 mg/ml. It is postulated that the alcohol-induced increase in plasma estradiol is due to changes in hepatic redox states associated with the catabolism of ethanol.
Pharmacology, Biochemistry and Behavior | 1988
Nancy K. Mello; Jack H. Mendelson; Mark P. Bree; Alicja Skupny
The long-acting opioid antagonist, naltrexone, stimulates LH and FSH in women during the early follicular phase of the menstrual cycle and is a new provocative test of hypothalamic-pituitary function (42,63). The acute effects of naltrexone (0.25, 0.50 and 1.0 mg/kg IV) on anterior pituitary (LH, FSH, PRL) and gonadal steroid (T or E2) hormones were studied in 7 female and 4 male rhesus monkeys (Macaca mulatta). Integrated plasma samples were collected at 20 min intervals for 60 min before and for 300 min after intravenous infusion of naltrexone over 10 min. In females studied during the early follicular phase (cycle days 1-3), naltrexone did not stimulate LH and significantly suppressed E2 (p less than 0.0003-0.0001) and FSH (p less than 0.006-0.0001). Naltrexone (0.50 and 1.0 mg/kg) also did not stimulate LH release in late follicular phase females (cycle days 10-12) when estradiol levels were in the peri-ovulatory range. FSH and E2 were significantly suppressed (p less than 0.01-0.05) after 1.0 mg/kg naltrexone, but not after 0.5 mg/kg naltrexone. However, in males all doses of naltrexone significantly stimulated LH (p less than 0.003-0.0001) and T (p less than 0.001-0.0001) but not FSH. LH increased significantly above baseline within 20 to 40 min and T increased significantly within 60 min. These gender differences in naltrexones effects on pituitary gonadotropins and gonadal steroid hormones were unanticipated. These data are not concordant with clinical studies which report significant naltrexone stimulation of LH in men and in women during the early follicular phase.(ABSTRACT TRUNCATED AT 250 WORDS)
American Journal of Psychiatry | 1988
Jack H. Mendelson; Siew Koon Teoh; Ulrike Lange; Nancy K. Mello; Roger D. Weiss; Alicja Skupny; James Ellingboe
The Journal of Clinical Endocrinology and Metabolism | 1988
Siew Koon Teoh; Jack H. Mendelson; Nancy K. Mello; Alicja Skupny
Journal of Pharmacology and Experimental Therapeutics | 1990
Siew Koon Teoh; Jack H. Mendelson; Mello Nk; Alicja Skupny; James Ellingboe
Journal of Pharmacology and Experimental Therapeutics | 1988
Mello Nk; Jack H. Mendelson; Mark P. Bree; Alicja Skupny
NIDA research monograph | 1988
Jack H. Mendelson; Siew Koon Teoh; Ulrike Lange; Mello Nk; Roger D. Weiss; Alicja Skupny
Pharmacology, Biochemistry and Behavior | 2007
Nathalie V. Goletiani; Jack H. Mendelson; Michelle B. Sholar; Arthur J. Siegel; Alicja Skupny; Nancy K. Mello
Alcohol | 1989
Nancy K. Mello; Jack H. Mendelson; Mark P. Bree; Alicja Skupny
NIDA research monograph | 1988
Mello Nk; Jack H. Mendelson; Mark P. Bree; Alicja Skupny