PMID- 20348138 OWN - NLM STAT- MEDLINE DCOM- 20101215 LR - 20171116 IS - 1755-3245 (Electronic) IS - 0008-6363 (Linking) VI - 87 IP - 4 DP - 2010 Sep 1 TI - Gender-specific effects of caloric restriction on the balance of vascular nitric oxide and superoxide radical. PG - 751-9 LID - 10.1093/cvr/cvq095 [doi] AB - AIMS: Caloric restriction (CR) and female gender attenuate oxidative damage and improve vascular endothelium-dependent relaxation (EDR). Multiple mechanisms that ameliorate vascular O(2)(*-) could enhance the NO(*)/O(2)(*-) balance and thus improve EDR. The aim of this study is to compare the effects of short-term (2 weeks) CR and gender on molecular mechanisms involved in NO(*)/O(2)(*-) balance and EDR. METHODS AND RESULTS: Wistar rats (8 weeks old) of both genders were fed ad libitum (control) or were subjected to CR (60% of food intake of controls) for 2 weeks. Plasma levels of NO(*), insulin, and ghrelin, EDR, vascular NO(*) and O(2)(*-) production, as well as endothelial NO(*) synthase (eNOS) and NADPH oxidase (Nox) expression were examined and analysed. CR improved EDR and vascular NO(*) levels and ameliorated NADPH-sensitive O(2)(*-) production in male rats more than in females. Both CR and female gender reduced mRNA expression of Nox1 and Nox p22phox (p22phox); however, CR reduced Nox4 and p47phox only in males. Protein expression studies showed that CR enhanced eNOS and reduced Nox4 only in males. CONCLUSION: Short-term CR improved the NO(*)/O(2)(*-) balance by lowering vascular O(2)(*-) production through decreased expression of Nox in males, thus enhancing bioactive NO(*) levels and EDR. In this regard, CR shifted the state of vascular NO(*)/O(2)(*-) balance in males to a state similar to that in females. FAU - Chou, Shih-Hsuan AU - Chou SH AD - Department of Physiology and Pharmacology, Chang Gung University, Taoyuan, Taiwan, Republic of China. FAU - Lee, Yung-Chen AU - Lee YC FAU - Huang, Chiu-Feng AU - Huang CF FAU - Wang, Yu-Ren AU - Wang YR FAU - Yu, Huang-Ping AU - Yu HP FAU - Lau, Ying-Tung AU - Lau YT LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100325 PL - England TA - Cardiovasc Res JT - Cardiovascular research JID - 0077427 RN - 0 (Ghrelin) RN - 0 (Insulin) RN - 0 (RNA, Messenger) RN - 0 (Vasodilator Agents) RN - 11062-77-4 (Superoxides) RN - 31C4KY9ESH (Nitric Oxide) RN - EC 1.14.13.39 (Nitric Oxide Synthase Type III) RN - EC 1.14.13.39 (Nos3 protein, rat) RN - EC 1.6.3.- (NADPH Oxidases) SB - IM MH - Animals MH - Aorta/drug effects/*metabolism MH - *Caloric Restriction MH - Dose-Response Relationship, Drug MH - Female MH - Gene Expression Regulation, Enzymologic MH - Ghrelin/blood MH - Insulin/blood MH - Male MH - NADPH Oxidases/genetics/metabolism MH - Nitric Oxide/blood/*metabolism MH - Nitric Oxide Synthase Type III/genetics/metabolism MH - RNA, Messenger/metabolism MH - Rats MH - Rats, Wistar MH - Sex Factors MH - Superoxides/*metabolism MH - Time Factors MH - *Vasodilation MH - Vasodilator Agents/pharmacology EDAT- 2010/03/30 06:00 MHDA- 2010/12/16 06:00 CRDT- 2010/03/30 06:00 PHST- 2010/03/30 06:00 [entrez] PHST- 2010/03/30 06:00 [pubmed] PHST- 2010/12/16 06:00 [medline] AID - cvq095 [pii] AID - 10.1093/cvr/cvq095 [doi] PST - ppublish SO - Cardiovasc Res. 2010 Sep 1;87(4):751-9. doi: 10.1093/cvr/cvq095. Epub 2010 Mar 25.