Literature DB >> 25181356

Different effect of l-NAME treatment on susceptibility to decompression sickness in male and female rats.

Aleksandra Mazur1, Peter Buzzacott, Kate Lambrechts, Qiong Wang, Marc Belhomme, Michael Theron, Georgi Popov, Giovanni Distefano, Francois Guerrero.   

Abstract

Vascular bubble formation results from supersaturation during inadequate decompression contributes to endothelial injuries, which form the basis for the development of decompression sickness (DCS). Risk factors for DCS include increased age, weight-fat mass, decreased maximal oxygen uptake, chronic diseases, dehydration, and nitric oxide (NO) bioavailability. Production of NO is often affected by diving and its expression-activity varies between the genders. Little is known about the influence of sex on the risk of DCS. To study this relationship we used an animal model of Nω-nitro-l-arginine methyl ester (l-NAME) to induce decreased NO production. Male and female rats with diverse ages and weights were divided into 2 groups: treated with l-NAME (in tap water; 0.05 mg·mL(-1) for 7 days) and a control group. To control the distribution of nitrogen among tissues, 2 different compression-decompression protocols were used. Results showed that l-NAME was significantly associated with increased DCS in female rats (p = 0.039) only. Weight was significant for both sexes (p = 0.01). The protocol with the highest estimated tissue pressures in the slower compartments was 2.6 times more likely to produce DCS than the protocol with the highest estimated tissue pressures in faster compartments. The outcome of this study had significantly different susceptibility to DCS after l-NAME treatment between the sexes, while l-NAME per se had no effect on the likelihood of DCS. The analysis also showed that for the appearance of DCS, the most significant factors were type of protocol and weight.

Entities:  

Keywords:  animal model; biodisponibilité de l’oxyde nitrique; diving; facteurs de risque; hyperbare; hyperbaric exposure; mal de décompression; nitric oxide bioavailability; plongée; rat; risk factors; sex; sexe

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Year:  2014        PMID: 25181356     DOI: 10.1139/apnm-2014-0148

Source DB:  PubMed          Journal:  Appl Physiol Nutr Metab        ISSN: 1715-5312            Impact factor:   2.665


  5 in total

1.  Preventive effect of rosiglitazone on liver injury in a mouse model of decompression sickness.

Authors:  Bin Peng; Miao-Miao Chen; Zheng-Lin Jiang; Xia Li; Guo-Hua Wang; Li-Hua Xu
Journal:  Diving Hyperb Med       Date:  2017-03       Impact factor: 0.887

2.  Blood pressure in rats selectively bred for their resistance to decompression sickness.

Authors:  Emmanuel Dugrenot; Jérémy Orsat; François Guerrero
Journal:  Diving Hyperb Med       Date:  2022-06-30       Impact factor: 1.228

3.  A Single Simulated Heliox Dive Modifies Endothelial Function in the Vascular Wall of ApoE Knockout Male Rats More Than Females.

Authors:  Simin Berenji Ardestani; Vladimir V Matchkov; Ingrid Eftedal; Michael Pedersen
Journal:  Front Physiol       Date:  2019-10-22       Impact factor: 4.566

4.  Editorial: Cardio-vascular Dysfunction and Physiological Manifestations Induced by Environmental Conditions.

Authors:  Marc-Antoine Custaud; Olga Vinogradova; Claude Gharib; Michael Delp; François Guerrero; Ronan Murphy
Journal:  Front Physiol       Date:  2022-03-17       Impact factor: 4.566

5.  Angiotensin Converting Enzyme Inhibitor Has a Protective Effect on Decompression Sickness in Rats.

Authors:  Aleksandra Mazur; Anthony Guernec; Jacky Lautridou; Julie Dupas; Emmanuel Dugrenot; Marc Belhomme; Michael Theron; François Guerrero
Journal:  Front Physiol       Date:  2018-03-01       Impact factor: 4.566

  5 in total

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