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J Sex Med ; 5(2): 336-43, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18179459

ABSTRACT

INTRODUCTION: Cyclic guanosine monophosphate (cGMP) levels can be regulated by heme oxygenase-1 and 2 (HO-1 and HO-2)-derived carbon monoxide (CO). AIMS: Assessment of the effect of upregulating CO in rat corpora cavernosa (CC) on cavernous cGMP. METHODS: Three experimental groups were studied: first group (N = 40), short-term HO induction over 2 weeks by injection of intraperitoneal increasing doses of hemin; the second group (N = 40) was subjected to intracavernosal injection of CO donor, CORM-3, or its inactive form (iCORM-3) over 2 weeks; the third group (N = 60) was subdivided into three subgroups: the first one received a combined hemin and CORM-3, the second one received hemin and its inhibitor stannus mesoporphyrin (SnMP), and third one received a combined hemin, CORM-3, and SnMP. MAIN OUTCOME MEASURES: In CC, HO-1 and HO-2 gene expression, Northern blot and Western blot, cGMP levels, and HO enzyme activity. RESULTS: In the first group, maximum induction of HO-1 gene expression, HO enzyme activity, and cGMP occurred with 4-mg hemin dose with a successive increase over 2 weeks. In the second group, CORM-3 increased cGMP by twofold compared with iCORM-3, and also increased HO-1 protein. In the third group, SnMP inhibited the enhancing effect of CORM-3 and HO on erectile signaling molecules; i.e., HO-1 gene, enzyme activity, and cGMP. CONCLUSIONS: CORM-3- or hemin-mediated CO release could increase cavernous tissue cGMP.


Subject(s)
Cyclic GMP/metabolism , Hemin/administration & dosage , Muscle, Smooth, Vascular/metabolism , Organometallic Compounds/administration & dosage , Penis/metabolism , Animals , Blotting, Northern , Blotting, Western , Carbon Monoxide/metabolism , Diphosphates/pharmacology , Dose-Response Relationship, Drug , Drug Administration Schedule , Heme Oxygenase (Decyclizing)/metabolism , Heme Oxygenase-1/metabolism , Injections, Intraperitoneal , Male , Mesoporphyrins/pharmacology , Muscle, Smooth, Vascular/drug effects , Rats , Rats, Sprague-Dawley , Up-Regulation
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