Back to Authors

Ferber, Irene

Mayo Clinic

Gastroenterology Research Unit and Enteric Neurosciences Program,

Citations 2

Viscoelastic properties of the human colon
Bharucha, Adil E. , Hubmayr, Rolf D., Ferber, Irene, Zinsmeister, Alan R.

American Journal of Physiology-Gastrointestinal and Liver Physiology | December 24, 2017 | Volume: 281 | Issue: 2 | Pages: G459-G466

10.1152/ajpgi.2001.281.2.g459 Get It

Our objectives were to characterize colonic viscoelastic properties of the human descending colon by assessing pressure-volume (P-V) relationships during barostatic balloon distension. In 16 healthy subjects, a balloon was inflated to 44 mmHg and then deflated to 0 mmHg in 4-mmHg steps at 10, 30, and 60 ml/min, allowing volume fluctuations to stabilize at each pressure increment. Thereafter, these “quasi-static” P-V curves were compared with “dynamic” distensions to 300 ml, at 1 and 10 ml/s, before and after intravenous atropine in another five subjects. During quasi-static curves, balloon volume stabilized at each pressure increment. Quasi-static P-V curves were reproducible within individuals and approximated to a power exponential function and revealed hysteresis, indicative of viscoelasticity. Body mass index influenced quasi-static P-V curves during inflation but not during deflation. The colon was less compliant during dynamic distensions at 10 ml/s than during quasi-static distensions. Atropine increased quasi-static compliance and attenuated differences between quasi-static and rapid distensions. We conclude that colonic viscoelastic properties can be assessed by quasi-static P-V curves. Rapid colonic distension activated neural reflexes, thereby reducing colonic compliance compared with quasi-static distensions.
Effects of a κ-opioid agonist, asimadoline, on satiation and GI motor and sensory functions in humans
Delgado-Aros, Sílvia, Chial, Heather J., Camilleri, Michael , Szarka, Lawrence A., Weber, Frank T., Jacob, Jutta, Ferber, Irene, McKinzie, Sanna, Burton, Duane D. , Zinsmeister, Alan R.

American Journal of Physiology-Gastrointestinal and Liver Physiology | March 3, 2015 | Volume: 284 | Issue: 4 | Pages: G558-G566

10.1152/ajpgi.00360.2002 Get It

To compare the effects of the κ-opioid agonist asimadoline and placebo on visceral sensation and gastrointestinal (GI) motor functions in humans, 91 healthy participants were randomized in a double-blind fashion to 0.15, 0.5, or 1.5 mg of asimadoline or placebo orally twice a day for 9 days. We assessed satiation (nutrient drink test), colonic compliance, tone, perception of colonic distension (barostat), and whole gut transit (scintigraphy). Treatment effect was assessed by analysis of covariance. Asimadoline increased nutrient drink intake ( P = 0.03). Asimadoline decreased colonic tone during fasting ( P = 0.03) without affecting postprandial colonic contraction, compliance, or transit. Gas scores in response to colonic distension were decreased with 0.5 mg of asimadoline at low levels (8 mmHg above operating pressure) of distension ( P = 0.04) but not at higher levels of distension. Asimadoline at 1.5 mg increased gas scores at 16 mmHg of distension ( P = 0.03) and pain scores at distensions of 8 and 16 mmHg ( P = 0.003 and 0.03, respectively) but not at higher levels of distension. Further studies of this compound in diseases with altered satiation or visceral sensation are warranted.