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      토끼 음경 해면체 평활근에서 Atropine의 약리작용과 기전 = The Action Mechanism of Relaxation Effect of Atropine on the Isolated Rabbit Corpus Cavernosum

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      https://www.riss.kr/link?id=A30045468

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      다국어 초록 (Multilingual Abstract)

      Atropine is the classic antimuscarinic anticholinergic grug that has been used to block cholinergic neurotransmission in basic research and received recent interest clinically in the intracavemous pharmacotherapy of erectile dysfunction. It has been suggested that at low dose(10^-8M), atropine blocks muscarinic receptors, thereby reducing both cholinergic of the adrenergic and cholinergic excitation of the NANC neuroeffector systems, on the other hand, at large pharmacologic dose(10^-3M), induces the release of EDRF which recently has been identified as nitric oxide(NO) of NO like substance. Therefore, we tried to confirm the action of atropine in the cavernosal tissue and define its mechanism.
      Strips of rabbit corpus cavernosum were isolated and mounted in 10ml organ chambers to measure isometric tension. Muscle strips submaximally precontracted with phenylephrine(5×10^-6M) and treated with increasing concentrations of atropine(10^-11M to 10^-3M) showed tension increase upto 10^-8M of atropine, and thereafter, relaxed concentration-dependently(10^-7: 43.7%, 10^-6M: 63.0%, 10^-5M: 86.2%, 10^-4M: 93.6%, 10^-3M: 100%). Relaxations to atropine(5×10^-6M) were not inhibited even partially by endothelial disruption or by pretreatment with methylene blue or pyrogallol. Pretreatment of muscle strips with atropine(5×10^-6M) caused concentration-related inhibition of a phenylephrine induced contraction, and in calcium-free high potassium depolarizing solution, decreased basal tension as well as inhibited contraction induced by CaCl_2. However, atropine did not produce reduction of responses to depolarizing medium(20, 40, 80mM KCl).
      With these results we can confirm the relaxation effect of atropine at a larger dose(>10^-7M) on the cavernosal smooth muscle and suggest that its action is mediated by increasing intracellular calcium sequestration, not by hyperpolarization or EDRF.
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      Atropine is the classic antimuscarinic anticholinergic grug that has been used to block cholinergic neurotransmission in basic research and received recent interest clinically in the intracavemous pharmacotherapy of erectile dysfunction. It has been s...

      Atropine is the classic antimuscarinic anticholinergic grug that has been used to block cholinergic neurotransmission in basic research and received recent interest clinically in the intracavemous pharmacotherapy of erectile dysfunction. It has been suggested that at low dose(10^-8M), atropine blocks muscarinic receptors, thereby reducing both cholinergic of the adrenergic and cholinergic excitation of the NANC neuroeffector systems, on the other hand, at large pharmacologic dose(10^-3M), induces the release of EDRF which recently has been identified as nitric oxide(NO) of NO like substance. Therefore, we tried to confirm the action of atropine in the cavernosal tissue and define its mechanism.
      Strips of rabbit corpus cavernosum were isolated and mounted in 10ml organ chambers to measure isometric tension. Muscle strips submaximally precontracted with phenylephrine(5×10^-6M) and treated with increasing concentrations of atropine(10^-11M to 10^-3M) showed tension increase upto 10^-8M of atropine, and thereafter, relaxed concentration-dependently(10^-7: 43.7%, 10^-6M: 63.0%, 10^-5M: 86.2%, 10^-4M: 93.6%, 10^-3M: 100%). Relaxations to atropine(5×10^-6M) were not inhibited even partially by endothelial disruption or by pretreatment with methylene blue or pyrogallol. Pretreatment of muscle strips with atropine(5×10^-6M) caused concentration-related inhibition of a phenylephrine induced contraction, and in calcium-free high potassium depolarizing solution, decreased basal tension as well as inhibited contraction induced by CaCl_2. However, atropine did not produce reduction of responses to depolarizing medium(20, 40, 80mM KCl).
      With these results we can confirm the relaxation effect of atropine at a larger dose(>10^-7M) on the cavernosal smooth muscle and suggest that its action is mediated by increasing intracellular calcium sequestration, not by hyperpolarization or EDRF.

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