Abstract
The study was performed to clarify if apomorphine at the level of the rat corpus cavernosum can produce erectile responses or interfere with nerve-induced penile erection. Apomorphine (10 -9-10 -4 M) exhibited a 10-fold higher potency to relax phenylephrine (Phe)- than endothelin-1 (ET-1)-induced contractions. Relaxant effects of apomorphine in Phe-activated corpus cavernosum did not change tissue levels of cyclic nucleotides, and were unaffected by inhibition of the synthesis of nitric oxide, or by inhibition of the soluble guanylate cyclase. Relaxations by apomorphine of ET-1-contracted rat corpus cavernosum were not influenced by α 2-adrenoceptor blockade (yohimbine, 10 -7 M), or by the dopamine D1-like receptor antagonist SCH 23390 (10 -6 M). Clozapine (10 -6 M), a proposed dopamine D2-like receptor antagonist, partly reduced apomorphine-induced relaxations, and significantly altered the -log IC 50 value for apomorphine. Nerve-induced contractions of the rat corpus cavernosum were attenuated by apomorphine in a concentration-dependent and biphasic manner. Yohimbine (10 -7 M) abolished the biphasic concentration-response pattern. SCH 23390 (10 -6 M) attenuated the inhibitory effects of apomorphine on contractions, and significantly altered the -log IC 50 value for the compound. In anesthetized rats (50 mg kg -1 pentobarbital sodium, 10 mg kg -1 ketamine), intracavernous apomorphine (100, 300, or 1000 nmol) did not have effects on basal cavernous pressure under resting conditions, and did not affect filling or emptying rates, or peak pressures of the rat corpus cavernosum during submaximal activation of the cavernous nerve. In awake rats, apomorphine produced a maximal number of erections at 300 nmol kg -1. In the rat isolated corpus cavernosum, pre- and postjunctional effects of apomorphine appear to involve dopamine D1- and D2-like receptors, as well as α-adrenoceptors. At relevant systemic doses of apomorphine, peripheral effects of the compound are unlikely to contribute to its proerectile effects in rats.
| Original language | English |
|---|---|
| Pages (from-to) | 259-267 |
| Number of pages | 9 |
| Journal | British Journal of Pharmacology |
| Volume | 146 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 2005 |
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Keywords
- α-adrenoceptors
- Apomorphine
- Corpus cavernosum
- Dopamine receptors
- Rat
- Relaxation
ASJC Scopus subject areas
- Pharmacology
Cite this
Effects in vitro and in vivo by apomorphine in the rat corpus cavernosum. / Matsumoto, Kenshi; Yoshida, Masaki; Andersson, Karl Erik; Hedlund, Petter.
In: British Journal of Pharmacology, Vol. 146, No. 2, 2005, p. 259-267.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Effects in vitro and in vivo by apomorphine in the rat corpus cavernosum
AU - Matsumoto, Kenshi
AU - Yoshida, Masaki
AU - Andersson, Karl Erik
AU - Hedlund, Petter
PY - 2005
Y1 - 2005
N2 - The study was performed to clarify if apomorphine at the level of the rat corpus cavernosum can produce erectile responses or interfere with nerve-induced penile erection. Apomorphine (10 -9-10 -4 M) exhibited a 10-fold higher potency to relax phenylephrine (Phe)- than endothelin-1 (ET-1)-induced contractions. Relaxant effects of apomorphine in Phe-activated corpus cavernosum did not change tissue levels of cyclic nucleotides, and were unaffected by inhibition of the synthesis of nitric oxide, or by inhibition of the soluble guanylate cyclase. Relaxations by apomorphine of ET-1-contracted rat corpus cavernosum were not influenced by α 2-adrenoceptor blockade (yohimbine, 10 -7 M), or by the dopamine D1-like receptor antagonist SCH 23390 (10 -6 M). Clozapine (10 -6 M), a proposed dopamine D2-like receptor antagonist, partly reduced apomorphine-induced relaxations, and significantly altered the -log IC 50 value for apomorphine. Nerve-induced contractions of the rat corpus cavernosum were attenuated by apomorphine in a concentration-dependent and biphasic manner. Yohimbine (10 -7 M) abolished the biphasic concentration-response pattern. SCH 23390 (10 -6 M) attenuated the inhibitory effects of apomorphine on contractions, and significantly altered the -log IC 50 value for the compound. In anesthetized rats (50 mg kg -1 pentobarbital sodium, 10 mg kg -1 ketamine), intracavernous apomorphine (100, 300, or 1000 nmol) did not have effects on basal cavernous pressure under resting conditions, and did not affect filling or emptying rates, or peak pressures of the rat corpus cavernosum during submaximal activation of the cavernous nerve. In awake rats, apomorphine produced a maximal number of erections at 300 nmol kg -1. In the rat isolated corpus cavernosum, pre- and postjunctional effects of apomorphine appear to involve dopamine D1- and D2-like receptors, as well as α-adrenoceptors. At relevant systemic doses of apomorphine, peripheral effects of the compound are unlikely to contribute to its proerectile effects in rats.
AB - The study was performed to clarify if apomorphine at the level of the rat corpus cavernosum can produce erectile responses or interfere with nerve-induced penile erection. Apomorphine (10 -9-10 -4 M) exhibited a 10-fold higher potency to relax phenylephrine (Phe)- than endothelin-1 (ET-1)-induced contractions. Relaxant effects of apomorphine in Phe-activated corpus cavernosum did not change tissue levels of cyclic nucleotides, and were unaffected by inhibition of the synthesis of nitric oxide, or by inhibition of the soluble guanylate cyclase. Relaxations by apomorphine of ET-1-contracted rat corpus cavernosum were not influenced by α 2-adrenoceptor blockade (yohimbine, 10 -7 M), or by the dopamine D1-like receptor antagonist SCH 23390 (10 -6 M). Clozapine (10 -6 M), a proposed dopamine D2-like receptor antagonist, partly reduced apomorphine-induced relaxations, and significantly altered the -log IC 50 value for apomorphine. Nerve-induced contractions of the rat corpus cavernosum were attenuated by apomorphine in a concentration-dependent and biphasic manner. Yohimbine (10 -7 M) abolished the biphasic concentration-response pattern. SCH 23390 (10 -6 M) attenuated the inhibitory effects of apomorphine on contractions, and significantly altered the -log IC 50 value for the compound. In anesthetized rats (50 mg kg -1 pentobarbital sodium, 10 mg kg -1 ketamine), intracavernous apomorphine (100, 300, or 1000 nmol) did not have effects on basal cavernous pressure under resting conditions, and did not affect filling or emptying rates, or peak pressures of the rat corpus cavernosum during submaximal activation of the cavernous nerve. In awake rats, apomorphine produced a maximal number of erections at 300 nmol kg -1. In the rat isolated corpus cavernosum, pre- and postjunctional effects of apomorphine appear to involve dopamine D1- and D2-like receptors, as well as α-adrenoceptors. At relevant systemic doses of apomorphine, peripheral effects of the compound are unlikely to contribute to its proerectile effects in rats.
KW - α-adrenoceptors
KW - Apomorphine
KW - Corpus cavernosum
KW - Dopamine receptors
KW - Rat
KW - Relaxation
UR - http://www.scopus.com/inward/record.url?scp=30544445518&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=30544445518&partnerID=8YFLogxK
U2 - 10.1038/sj.bjp.0706317
DO - 10.1038/sj.bjp.0706317
M3 - Article
C2 - 16025145
AN - SCOPUS:30544445518
VL - 146
SP - 259
EP - 267
JO - British Journal of Pharmacology
JF - British Journal of Pharmacology
SN - 0007-1188
IS - 2
ER -