Further evidence for the role of nitric oxide in maternal aggression: effects of L-NAME on maternal aggression towards female intruders in Wistar rats
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
18657004
DOI
10.33549/physiolres.931540
PII: 1540
Knihovny.cz E-resources
- MeSH
- Aggression drug effects MeSH
- Behavior, Animal drug effects MeSH
- Enzyme Inhibitors pharmacology MeSH
- Rats MeSH
- Maternal Behavior drug effects MeSH
- NG-Nitroarginine Methyl Ester pharmacology MeSH
- Nitric Oxide metabolism MeSH
- Rats, Wistar MeSH
- Nitric Oxide Synthase antagonists & inhibitors metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Enzyme Inhibitors MeSH
- NG-Nitroarginine Methyl Ester MeSH
- Nitric Oxide MeSH
- Nitric Oxide Synthase MeSH
It has been shown that nitric oxide (NO) increases aggression in male mice, whereas it decreases aggression in lactating female mice and prairie voles. It is also known that aggression can be exhibited at different levels in rodent species, strain or subtypes. The aims of this study were to investigate the proportion of aggressiveness in Wistar rats, the effect of intraperitoneally administered nonspecific nitric oxide synthase (NOS) inhibitor L-NAME (NG-nitro L-arginine methyl ester) on maternal aggression towards female intruders, and whether these effects are due to NO production or not. Rats were given saline intraperitoneally on the postpartum Day 2 and aggression levels were recorded. The same rats were given 60 mg/kg L-NAME or D-NAME (NG-nitro D-arginine methyl ester) on the postpartum Day 3 and their effects on aggression levels were compared to saline. While L-NAME administration did not cause any differences in the total number of aggressive behavior, aggression duration and aggression intensity, it reduced the proportion of animals showing aggressive behavior. In addition, the latency of the first aggression was significantly increased by L-NAME. In the D-NAME group, however, no significant change was found. Our results have shown that L-NAME reduces maternal aggression towards female intruders in Wistar rats through inhibition of NO production. These results suggest that the role of NO in offensive and defensive maternal aggression shares neural mechanisms.
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