• 제목/요약/키워드: vas deference

검색결과 7건 처리시간 0.021초

Clonidine의 혈압강하및 적출정관 평활근수축에 미치는 6-Hydroxydopamine의 영향 (The Effect of 6-Hydroxydopamine on the Hypotensive Action and Contractile Force of Isolated Vas Deferens Smooth Muscle by Clonidine)

  • 윤재순;장문희
    • 약학회지
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    • 제31권2호
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    • pp.82-91
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    • 1987
  • The effect of neurotoxic compound 6-hydroxydopamine (6-OHDA) on the change in blood pressure and contractile response of Vas deference by centrally acting agents has been studied in normal and DOCA-salt induced hypertensive rats. The treatment of neonatal rats with 6-OHDA (2$\times$100mg, 250mg Kg$^{-1}$s.c) significantly inhibited the antihypertensive and relaxant effects of Vas deference of clonidine(100$\mu\textrm{g}$ Kg$^{-1}$iv.). The simultaneous administration of desipramine with clonidine into neonatal rats decreased the antihypertensive response of clonidine although treated did not affect the relaxative response of Vas deference. Furthermore, the antihypertensive and relaxant responses of clonidine were reduced by the neonatal rats with 6-OHDA regardless of the administration of desipramine. When neonatal rats were administered with 6-OHDA, the development of DOCA-salt hypertension was prevented. These results suggest that 6-OHDA, clonidine and desipramine hada significant effect on the development and the inhibition of central hypertension mediating the central adrenergic neuron due to their affinity to the central nervous system.

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소형견종에서 실시한 복강경 잠복고환 절제술 (Laparoscopic Cryptorchidectomy in Small Breed Dogs)

  • 박지영;정성목
    • 한국임상수의학회지
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    • 제31권1호
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    • pp.61-65
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    • 2014
  • The study aimed at determining the feasibility of three portal totally Laparoscopic cryptorchidectomy in small breed dogs. Four right sided and one left sided abdomen retained testicles in five dogs weighing 2.2~8.7 kg were retrieved successfully. Pampiniform plexus and vas deference were ligated and transected with Hem-o-lock/monopolar electrocauterization (1/5), or ultrasonic scalpel (4/5) and the latter provided more easy, quick and safe hemostasis and transection. The resected testis was easily removed through a insertion site. Mean surgical time was $19.9{\pm}15.2$ minutes and when the abdominal cavity was explored again, there were no major complications. The patient recovered favorably without unwilling events. This is the case report of laparoscopic cryptorchidectomies in small breed dogs weigh less than 10 kg. Laparoscopic cryptorchidectomy could be considered as an alternative in small animal surgery.

위장질환 치료용 의약조성물(DWP 301)의 일반약리작용 (General Pharmacology of DWP 301, a New Combined Drug for Gastroduodenal Diseases)

  • 임승욱;염제호;김영만;심점순;박남준;장병수;연제덕;김병오;강진석
    • Biomolecules & Therapeutics
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    • 제2권4호
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    • pp.347-360
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    • 1994
  • The general and some pharmacological actions of DWP 301 were investigated in animals and the following results were obtained. In central nervous system, DWP 301 had no effects on the pentobarbital induced anaesthesia, rotarod test, traction test, analgesic action, anticonvulsant action in mice and body temperature in rat. But DWP 301 showed a little decrease of locomotor activity at a dose of 3,000 mg/kg. From these results, DWP 301 was considered to have little pharmacological effect on the central nervous system. Furthermore, DWP 301 had no influences on the normal blood pressure and heart rate. DWP 301 showed no effect on the isolated guinea pig ileum, trachea, right atrium, and nonpregnant rat uterus. But, in the isolated guinea pig vas deference, DWP 301 had showed inhibitory effect on the contractions produced by norepinephrine. DWP 301 showed rise of gastric juice pH and decrease of urine volume. Also, DWP 301 had no effect on the gastrointestinal motility and blood aggregation. From these results, it is concluded that the general pharmacological effect of DWP 301 are similar to or weaker than M and AGA.

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Pharmacological Characterization of (10bS)-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline Oxalate (YSL-3S) as a New ${\alpha}_2$-Adrenoceptor Antagonist

  • Chung, Sung-Hyun;Yook, Ju-Won;Min, Byung-Jun;Lee, Jae-Yeol;Lee, Yong-Sup;Jin, Chang-Bae
    • Archives of Pharmacal Research
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    • 제23권4호
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    • pp.353-359
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    • 2000
  • ${\alpha}_2$-Adrenoceptor antagonists, which can enhance synaptic norepinephrine levels by blocking feedback inhibition processes, are potentially useful in the treatment of disease states such. as depression, memory impairment, impotence and sexual dysfunction. (10bS)-1,2,3,5,6,10b-Hexahydropyrrolo[2,1-a]isoquinoline oxalate (YSL-3S) was evaluated in several in vitro biological tests to establish its pharmacological profile of activities as an ${\alpha}_2$-adrenoceptor antagonist. Saturation binding assay revealed that$^{3}[H]$rauwolscine bound to the $\alpha$$_2$-adrenoceptors with a Kd value of 6.3$\pm$0.5 nM and a Bmax value of 25l$\pm$39 fmol/mg protein in rat cortical synaptic membranes. Competitive binding assay showed that YSL-3S inhibited the binding of$^3[H]$rauwolscine (1 nM) in a concentration-dependent manner with a Ki value of 98.2$\pm$12.1 nM while it did not inhibit the binding of [$^3$H]cytisine (1.25 nM) to neuronal nicotinic cholinergic receptors. The Ki values of yohimbine, clonidine and norepinephrine for $^3[H]$rauwolscine binding were 15.8$\pm$1.0, 40.1$\pm$5.9 and 40.0$\pm$11.5 nM, respectively. In addition, the binding affinity of YSL-3S for ${\alpha}_2$-adrenoceptors was higher than that of its antipode and the racemic mixture. The functional activity of YSL-3S at the presynaptic ${\alpha}_2$-adrenoceptors was assessed using the prostatic portion of the rat vas deferens. Clonidine inhibited field-stimulated contractions of the vas deference in a dose-dependent manner. The presence of YSL-3S or yohimbine caused a parallel, rightward the dose-response curve of clonidine in a dose-dependent manner, indicating an antagonistic action at the presynaptic ${\alpha}_2$-adrenoceptors. The $pA_2$values of yohimbine and YSL-3S were 7.66$\pm$0.13 and 6.64$\pm$0.18, respectively. The results indicate that YSL-3S acts as a competitive antagonist at presynaptic ${\alpha}_2$ -adrenoceptors with a potency approximately ten times lower than yohimbine, but is devoid of binding affinity for neuronal nicotinic cholinergic receptors.

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위장질환 치료용 의약조성물(BWP 302)의 일반약리작용 (General Pharmacology of DWP 302, a New Combined Drug for Gastroduodenal Diseases)

  • 임승욱;염제호;김영만;장병수;남권호;김동오;유영효;박명환
    • Biomolecules & Therapeutics
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    • 제1권2호
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    • pp.211-219
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    • 1993
  • The general and some pharmacological actions of DWP 302 were investigated in animals and the following results were obtained. In central nervous system, DWP 302 had no effects on the pentobarbital induced anaesthesia, locomotor activity, rotarod test, traction test, analgesic action in the mice and body temperature in the rat. DWP 302 showed no depressive action on the convulsion induced by strychnine and electronic shock. From these results, DWP 302 was considered to have no or little pharmacological effect on the central nervous system. Furthermore, DWP 302 had no influences on the normal blood pressure and heart rate. In the isolated ileum of guinea pig, DWP 302 showed neither contractive nor relaxing effects against the acetylcholine ($10^{-6}g/mι$), histamine ($10^{-6}g/mι$) and $BaCl_2$ ($10^{-4}g/mι$) at a concentration of $1.9{\times}10^{-4}g/mι$ in bath. But it caused a slight increase in basal tone at a concentration of $6.3{\times}10^{-4}g/mι$ and this effect was inhibited by atropine $10^{-7}g/mι.$ In the isolated trachea and vas deference, DWP 302 showed no effect on the contractions produced by histamine and norepinephrine, respectively. And DWP 302 showed no effect on the contractions produced by acetylcholine and oxytocin in the isolated nonpregnant rat uterus. DWP 302 had no effect on bile excretion, urine volume, pH and gastrointestinal motility, But, DWP 302 showed a significant inhibitory effect on gastric secretion in the rat.

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징거미새우, Macrobrachium nipponense 수컷 생식기의 구조 (Structure of the Male Reproductive System in the Freshwater Prawn Macrobrachium nipponense)

  • 김대현;한창희
    • 생명과학회지
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    • 제8권5호
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    • pp.582-588
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    • 1998
  • 징거미 새우의 정소는 한 쌍의 관으로 되어 있고, 정소의 중앙 후반부에서 기원된 수정관은 제 5보각의 기부에 위치한 생식공까지 연결되어 있다. 수정관은 기부, 나선부, 말단부, 사정관으로 구분되었다. 수정관은 simple columnar ephithelium, high columnar ephithelium, 종주근과 환상근으로 이루어져 있다. AG는 수정관의 말단부에서 사정관에 걸쳐 위치하고 있다. AG의 형태는 불규칙한 세포 덩어리로 되어져 있고, hematoxyline에 약하게 염색되는 염색질과 둥글고 커다란 핵을 가진다. 핵질과 세포질은 염기성 핵막을 경계로 쉽게 구분되나, 세포질과 세포질사이의 경계는 그 구별이 어렵다. 암컷의 복판에 부착된 정포는 호산성기질, 호염기성기질 그리고 호염기성기질에 싸여있는 한 쌍의 정자덩어리로 구성되어 있다. 성숙정자는 압정형태이고, 두부는 가운데 부분이 약간 오목한 원반형이고, 미부는 두부 중앙부 하단의 약간 볼록한 부분에서 연장된 하나의 spike를 이루고 있다. 정자의 크기는 두부의 직경이 약 8 $\mu$m, 미부의 길이가 약 10 $\mu$m였다.

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생쥐 태아 및 성체 조직에서의 N-Methylpurine-DNA Glycosylase 유전자의 발현 (Expression of N-Methylpurine-DNA Glycosylase Gene during Fetal Development and Adult in Mice)

  • 손태종;김남근;이숙환;한세열;고정재;박찬;이우식;이찬;이용희;차광열
    • 한국발생생물학회지:발생과생식
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    • 제3권1호
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    • pp.101-105
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    • 1999
  • N-Methylpurine-DNA glycosylase (MPG)는 DNA에서 N-methylpurine과 다른 손상된 purine기를 제거하는 DNA 회복 효소이다. 생쥐의 임신 8일 후의 태아조직부터 생후 400일까지의 조직들로부터 RT-PCR 방법으로 MPG mRNA 발현을 조사하였다. MPG mRNA는 태아 형성기동안 많은 양이 발현되었으며, 특히 15일에서 가장 높게 발현되었다. 태반에서의 MPG mRNA는 8 p.c. (post coitum)부터 18 p.c. 까지 계속적으로 감소하였다. 태아 형성기의 뇌와 간 조직에서 높은 mRNA 발현을 보였으나, 400일 되는 성체에서는 현저히 감소하였다. 부정소, 정낭, 정소, 정관, 난소, 난관 그리고 자궁 등의 생식기관에서의 MPG mRNA는 비교적 높게 발현되었고, 그들 중 부정소에서의 발현 정도가 가장 높았다. 이러한 결과들로 보아 MPG 유전자는 태아 발생단계 및 조직 특이적으로 발현됨을 알 수 있었다.

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