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You may submit the following Regular abstracts per meeting:

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Abstracts for invited presentations in Plenary, Special, or Meeting-in-a-Meeting sessions do not count against your allotment of Regular abstracts.

In addition, you may submit a Regular Research Contributed abstract (oral or iPoster/poster) to a Special Session or Meeting-in-a-Meeting session that is accepting contributed oral and/or poster presentations. This abstract does not count against your allotment of Regular abstracts, but acceptance is subject to approval by the session organizer. If your oral or iPoster/poster presentation is not accepted into the requested Special Session or Meeting-in-a-Meeting, it will be scheduled in a regular oral or iPoster/poster session unless doing so would cause you to exceed the number of abstracts permitted per meeting as described above.

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We will strictly adhere to the following deadlines:

3 October 2018 5 December

Plenary sessions are 50 minutes long; no other sessions or events are scheduled in parallel with them. To allow time for introductions, prize presentations, and question-and-answer (QA) periods, prize and invited lecturers should plan to speak for at most 40 minutes. Plenary speakers will receive special abstract and presentation instructions from the AAS Executive Office.

Regular, history, and education oral presentations, as well as dissertation oral presentations, are arranged by topic and are scheduled in 90-minute sessions of five to nine talks each. For a regular, history, or education oral presentation, allow five minutes for the talk and three minutes for QA. For a dissertation oral presentation, allow 15 minutes for the talk and 5 minutes for QA.

Regular, history, and education posters allow far more time and flexibility than the corresponding oral presentations and are the default presentation types. Posters are arranged by topic and are usually displayed for one full day, including about 90 minutes when very few other sessions or events are scheduled, though if circumstances permit, at some meetings they are displayed for multiple days.

Fourteen healthy subjects [seven men: age, 29 ± 3 yr; body mass index (BMI), 24.20 ± 0.94 kg/m 2 ; seven women: age, 27 ± 2 yr; BMI, 20.80 ± 0.88 kg/m 2 ; P < 0.05 for BMI] participated in the metabolic studies. In eight healthy subjects (two men and six women; age, 25 ± 1 yr), we determined the effect of water drinking on plasma osmolarity. All subjects were drug-free and nonsmoking. The institutional review board approved all studies, and written informed consent was obtained before study entry.

Subjects did not eat 12.5 h before and did not drink 1.5 h before testing. Three separate studies were conducted. In the first study, we assessed the effect of drinking 500 ml of water on energy expenditure and substrate oxidation rates by using indirect calorimetry. In the second study, we used the microdialysis technique to characterize the effect of drinking 500 ml of water on adipose tissue blood flow and metabolism. In a subgroup, studies were conducted twice, once after ingestion of placebo and once after ingestion of 100 mg of the β-adrenoreceptor blocker metoprolol (Stada Arzneimittel AG, Bad Vilbel, Germany). The medications were ingested in a single-blinded fashion 1 h before water drinking. In the third study, we determined venous plasma osmolarity at baseline and 30 and 60 min after water drinking.

Oxygen uptake and carbon dioxide production were measured by using a respiratory chamber to assess changes in energy expenditure, respiratory quotient (RQ; CO 2 produced/O 2 consumed), and carbohydrate and lipid oxidation rates, respectively. In previous studies in 16 healthy subjects, the maximal spontaneous change in metabolic rate over a 3-h period was 0.2 ± 0.09 kJ/min (3%). Throughout the study, subjects remained seated. After a run-in period of 15 min, resting energy expenditure was determined for 30 min. Then, the subjects ingested 500 ml water (22 C). In a subgroup, we also tested the effect of 500 ml of 37 C warm water. After completion of drinking, measurements were continued for another 90 min.

Microdialysis studies were conducted in the supine position as described previously ( 7 , 8 ). Briefly, one (systemic β-adrenoreceptor blockade) or two (local β-adrenoreceptor blockade) microdialysis probes were inserted into sc adipose tissue at the level of the umbilicus. Before insertion of the probes, the respective area was anesthetized superficially with EMLA cream (AstraZeneca GmbH, Wedel, Germany). On the day with systemic β-adrenoreceptor blockade, the subjects ingested metoprolol (Stada Arzneimittel AG) before testing, and the probe was perfused with Ringer’s solution (Serumwerke Bernburg AG, Bernburg, Germany) supplemented with 50 m m ethanol (B. Braun Melsungen AG, Melsungen, Germany), for monitoring changes in blood flow, and 10 μ m ascorbate (Jenapharm GmbH Co. KG, Jena, Germany). On the day with local β-adrenoreceptor blockade, the subjects ingested placebo before testing, and the perfusate for one microdialysis probe was supplemented with 100 n m of the nonselective β-adrenoreceptor blocker propranolol (Obsidan; ALPHARMA-ISIS, Langenfeld, Germany). CMA/60 microdialysis probes and CMA/102 microdialysis pumps (both from CMA Microdialysis AB, Solna, Sweden) were used. The flow rate was 2 μl/min.

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