𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Gentamicin alters nitric oxide production in semicircular canals and otolith organs

✍ Scribed by Kai Helling; Ulf-Rüdiger Heinrich; Lukas Heusgen; Jürgen Brieger; Irene Schmidtmann; Huige Li; Wolf J. Mann


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
133 KB
Volume
120
Category
Article
ISSN
0023-852X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Objectives/Hypothesis:

Intratympanic application of gentamicin is an important therapeutic option to control vertigo spells in Ménière's disease. Low doses eliminate the function of semicircular canal ampullae (SCCA) and saccule in most patients, although utricular function is maintained in many cases. Local alteration in free radical production might be responsible for these differences. Therefore, the gentamicin‐induced nitric oxide (NO) production was determined in an animal model using separate organ cultures of SCCA, saccule, and utricle.

Study Design:

Prospective pilot study in male guinea pigs.

Methods:

SCCA, saccule, and utricle of 28 guinea pigs were isolated and incubated separately for 6 hours in cell culture medium. Gentamicin was administered in two different concentrations (0.4 mg/mL and 0.8 mg/mL) to organ cultures of 16 animals. Tissues from 12 animals were used as controls. Nitric oxide was quantified by chemiluminescence.

Results:

Gentamicin led to an NO increase of about 70% in the saccule, an NO reduction of more than 70% in SCCA, and an NO reduction of 36% in the utricle.

Conclusions:

The selective effects of gentamicin on the NO production in the different sensory areas of the vestibular organ have to be taken into account in the therapy of Ménière's disease. Laryngoscope, 2010


📜 SIMILAR VOLUMES


Decreased macrophage-mediated cytotoxici
✍ Eduardo M. Sotomayor; Michael R. Dinapoli; Cesar Calderón; Arthur Colsky; Yang-X 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 French ⚖ 866 KB

## Abstract Peritoneal‐exudate macrophages (PEM) from mammarytumor‐bearing mice have impaired cytotoxic activity against syngeneic and allogeneic tumor targets. The ability of PEM from normal and tumor‐bearing mice to bind tumor targets was found to be similar in the presence or the absence of surr