• 제목/요약/키워드: Phenylhydrazine

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자성(雌性) 흰쥐에서 phenylhydrazine으로 유발된 용혈성 빈혈에 오미자 약침의 항빈혈효과 (Anti-anemic Effect of Aqueous Extracts of Fructus schisandrae on Phenylhydrazine-induced Hemolytic Anemia in Female Sprague-Dawley Rats)

  • 신혜숙;김이화;김창주
    • Korean Journal of Acupuncture
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    • 제19권1호
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    • pp.67-75
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    • 2002
  • 목적 : 자성(雌性) 흰쥐에서 phenylhydrazine으로 유발된 용혈성 빈혈에 오미자 약침의 항빈혈효과를 알아보기 위해서 적혈구수, hematocrit ratio, hemoglobin, 혈청 철함유량 및 serum total iron binding capacity (TIBC)를 관찰하였다. 방법 : 실험동물은 정상군, 대조군, 250 mg/kg 오미자 투여군 및 500 mg/kg 오미자 투여군으로 총 4개의 군으로 분류하였다. 정상군의 흰쥐는 아무런 처치도 하지 않았고, 대조군은 phenylhydrazine으로 용혈성 빈혈을 유발하였다. 오미자 투여군은 용혈성 빈혈을 유발한 후 7일간 매일 250 mg/kg 및 500 mg/kg의 용량으로 중완혈에 자침하였다. 결과 : 적혈구수, hematocrit ratio 및 hemoglobin은 대조군에서 정상군에 비해 감소한 반면 오미자 투여군은 증가하였다. 혈청 철함유량과 TIBC는 대조군에서 증가하였으나, 오미자 투여군에서는 감소하였다. 이러한 결과로 중완혈에 오미자 자침은 phenylhydrazine으로 유발된 용혈성 빈혈에서 항빈혈효과가 있는 것으로 사려된다.

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The effects of Sa-Mul-Tang (Si-Wu-Tang), a Traditional Chinese Medicine, on Phenylhydrazine-induced Anemic Rats

  • Ryu, Jong-Hoon;Yook, Chang-Soo
    • Biomolecules & Therapeutics
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    • 제9권1호
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    • pp.1-6
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    • 2001
  • Sa-Mul-Tang (Si-Wu-Tang, SMT), a kind of Chinese medicine, has been used for the hemato-deficient disease for hundreds of years. In this work, investigations on the anti-anemic activity of an aqueous extract of SMT were undertaken in order to find the pharmacological basis for the ethnomedical use of the formulation. Three kinds of Angelicase species, such as Angelica sinensis, Angelica acutiloba, and Angelica gigas, were used for preparing the water extracts of SMT. Anemic model rats were induced by the treatment of phenylhydrazine (40 mg/kg/day, i.p.) for 4 days. After the treatment of phenylhydrazine, rats were divided into several groups for their different treatment of three kinds of SMT. Red blood cell (RBC), hemoglobin (Hg), and hematocrit (Hct) were determined on the day 0, 3, 6, 10, 14 after the treatment of SMTs and erythrocytes deformabilities were also determined at the end of experiments. Oral administration of SMT (1g/kg/day) for 14 days did not ameliorate drug-induced anemic states evaluated by RBC counts, Hg contents, and Hct values. However, the erythrocyte deformabilities were improved in phenylhydrazine-treated group by the administragest that SMTs (p<0.05). Especially, these effects were high in the Angelica acutiloba group. These results suggest that SMTs have an ameliorative effect on blood rheology related to the blood stasis syndrome in oriental diagnostics not on the blood deficient states related to the anemic syndrome.

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청혈지황탕(淸血地黃湯)이 Phenylhydrazine으로 유발한 용혈성 빈혈 흰쥐에 미치는 영향 (Effects of Chunghyuljihwang-tang on Phenylhydrazine-induced Hemolytic Anemia in Rats)

  • 양형주;우홍정
    • 대한한의학회지
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    • 제32권1호
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    • pp.130-140
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    • 2011
  • Objectives: This study was performed in order to investigate the anti-hemolytic effect of Chunghyuljihwang-tang(CHJHT, Qingxuedihuang-tang) on phenylhydrazine-induced hemolytic anemia in Rats. Materials and Methods: Hemolytic anemia model of rats were induced by phenylhydrazine(PHZ, 40mg/kg/day, i.p.) for 3days. Male Sprague-Dawley rats were divided into three groups for their treatment. Normal group was injected normal saline for 3 days with distilled water(d.w.) orally, control group was injected PHZ for 3 days with d.w. and CHJHT group was injected PHZ for 3 days with administration of CHJHT for 10 days. RBC(Red blood cell), Hb(hemoglobin), mean corpuscular volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, reticulocyte were determined on day 0, 4, 7, 10. Body weight was investigated on day 0, 2, 4, 6, 8, 10 and the weight of spleen was measured on day 10. Results: For CHJHT group, the levels of RBC and Hb were significantly higher than control group on day 4, and the concentration of hemoglobin on day 7 was increased more than control group. Moreover, reticulocyte was significantly decreased on day 10 more than control group. These results could be concluded that CHJHT suppressed the hemolytic anemia by PHZ and improved hematological values of anemia earlier.

생약복합제제(生藥複合製劑)의 약효(藥效) 연구(硏究) (제19보)(第19報) -사물안신탕(四物安神湯)이 순환기계(循環器系) 및 Phenylhydrazine으로 유발(誘發)된 가토빈혈(家兎貧血)에 대한 영향(影響)- (Studies on the Efficacy of Combined Preparation of Crude Drug (XIX) -The effect of ‘Samulanshintang’ on the Cardiovascular System and Anemic Rabbits induced by Phenylhydrazine-)

  • 홍남두;이경섭;황의완;김남재
    • 생약학회지
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    • 제15권4호
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    • pp.188-193
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    • 1984
  • It was previously indicated that 'Samulanshintang' had been examined for effects of the anticonvulsive, antipyretic, analgesic, sedative and antispasmodic actions. In order to investigate the effect on the cardiovascular system and anemic rabbits induced by phenlhydrazine HCl, pharmacological studies have been carried out with extract. The results of this investigation were summarized as follows: The relaxation of bronchial smooth muscle and antihistamine action were recognized. Antihypertensive and vasodilating actions due to vascular smooth muscle relaxation were noted in frogs and rabbits. 'Samulanshintang' lowered the rate of anemia induced by phenylhydrazine and rapidly recovered from the anemia state.

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생쥐난자에 있어서 투명대 경화현상이 체외수정에 미치는 영향 III. Peroxidase Inhibitors와 Tyrosine Analogue 처리된 난자의 투명대 경화 현상과 체외수정 (Effect of Zona Hardening on In Vitro Fertilization in Mouse Oocytes III. Analysis of In Vitro Fertilization and Zona Hardening in Oocytes Treated with Peroxidase Inhibitors and Tyrosine Analogue)

  • 이상진;정길생
    • 한국가축번식학회지
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    • 제17권3호
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    • pp.183-191
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    • 1993
  • These experiments were carried out to investigate whether the enzyme is involved in zona hardening during normal activatin of the oocytes by sperm, and demonstrate peroxidase activity during in vitro fertilization of oocytes treated with peroxidase inhibitors(250 $\mu$M phenylhydrazine, 28mM sodium sulfite, 350mM glycine ethyl ester and 50mM sodium azide) and tyrosine analogue(12.5mM tyramine). Also, zona soluble properties of the ovarian oocytes incubated for 0, 5, 10 and 15 hr in the presence of pheylhydrazine or tyramine were studied by using $\alpha$-chymotrypsin. The results obtained from these experiments were summarized as follows ; 1. The rates of fertilizatin in control oocytes and oocytes treated with phenylhydrazine or tyramine were 69.8%, 62.3% and 88.2%, respectively. However in vitro fertilization in oocytes treated with three different peroxidase inhibitors, sodium sulfite, glycine ethyl ester and sodium azide, were not induced. The oocytes treated with phenylhydrazine had no significant effect on in vitro fertilization rate as compared to control. However there was a significantly different in fertilization between tyramine treated group and control group(P<0.01). 2. The zona solubility(t50) of control and fertilized oocytes in culture treated with phenylhydrazine or tyramine were 30.7, 26.0 and 16.3 min., respectively. Phenylhydrazine treated group and tyramine treated group had effect on inhibition of zona hardening as compared to control group. These results suggest that ovoperoxidase is involved in zona hardening during normal activation of the oocytes by sperm. 3. t50 of control oocytes and ovarian oocytes treated with phenylhydrazine or tyramine for 5, 10 and 15 hr in vitro were 14.0, 26.2 and 32.0 min., 14.5, 26.9 and 30.2 min., and 14.0, 24.3 and 31.2 min., respectively. These results suggest that zona hardening in ovarian oocytes matured for various times in vitro cannot be inhibited by peroxidase inhibitors and tyrosine analogue, that the spontaneous zona hardening incultured ovarian oocytes is not caused by the secretory products of cortical granules released during the cortical reaction, ovoperoxidase.

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Chloral-2-acetothienone과 Trichloroethylidene-2-acetothienone의 합성 및 Trichloroethylidene-2-acetothienone 과 Hydrazien 들과의 반응 (Synthesis of Chloral-2-acetothienone and Trichloroethylidene-2-acetothienone, and Reaction of Trichloroethylidene-2-acetothienone with Hydrazines)

  • 이효원;이윤영
    • 대한화학회지
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    • 제19권1호
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    • pp.38-42
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    • 1975
  • 2-Acetothienone과 chloral을 축합시켜 chloral-2-acetothienone을 생성하였으며 이것을 탈수하여 trichloroethylidene-2-acetohienone을 합성하였다. Trichloroethylidene-2-acetothienone과 phenylhydrazine 또는 치환된 phenylhydrazine들과의 반응으로 2-aryl-6-(2-thienyl)-3(2H)-pyridazinone들을 얻었으며 hydrazine과의 반응에서는 3-(2-thienyl)-5-trichloromethyl-2-pyrazoline이 합성되었다.

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Trichloroethylideneacetophenone과 hydrazine들의 반응 (I) pyrazoline 및 pyridazinone 유도체의 합성 (Reactions of trichloroethylideneacetophenone with hydrazines (I) synthesis of pyrazoline and pyridazinone derivatives)

  • 이윤영;이우영;장세희
    • 대한화학회지
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    • 제14권1호
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    • pp.61-64
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    • 1970
  • trichloroethylideneacetophenone과 hydrazine hydrate의 반응으로 3-phenyl-5-trichloromethyl-2-pyrazoline을 합성하였다. 또한 trichloroethylideneacetophenone과 phenylhydrazine 또는 치환된 phenylhydrazine의 반응으로 pyridazinone 유도체들을 합성하였다.

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2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone As a Redox Titrant

  • El-Brash, A.M.;El-Hussain, Laila A.
    • Archives of Pharmacal Research
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    • 제20권6호
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    • pp.597-601
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    • 1997
  • An oxidimetric titrant, 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone in anhydrous acetic acid is used for the semimicro-determination of hydrazine hydrate, phenylhydrazine hydrochloride, isoniazid and iproniazid phosphate in pure forms as well as in some pharmaceutical preparations containing isoniazid and iproniazid phosphate. The end point was detected potentiometrically using a platinum-calomel combination electrode. The results obtained are compared statistically with those obtained by the official methods and they are in good agreement.

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$\gamma$,$\gamma$,$\gamma$-Trichloroethylidene-m-Nitroacetophenone과 Hydrazine 들의 반응 (Reactions of $\gamma$,$\gamma$,$\gamma$-Trichloroethylidene-m-Nitroacetophenone with Hydrazines)

  • 이윤영;송석주
    • 대한화학회지
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    • 제17권1호
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    • pp.25-30
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    • 1973
  • $\gamma$,$\gamma$,$\gamma$-Trichloroethylidene-m-Nitroacetophenone과 phenylhydrazine및 치환된 phenylhydrazine들과의 반응으로 2,6-disubstituted-3-pyridazinone들을 합성하였으며 2,4-dinitrophenylhydrazine과의 반응에서는 hydrazone을 중간체로 분리하였다. hydrazinehydrate와의 반응에서는 3-(mnitrophenyl)-5-trichloromethyl-2-pyrazoline이 좋은 수득률로 얻어졌다. 또한$\gamma$,$\gamma$,$\gamma$-trichloroethylidene-m-nitroacetophenone과 치환된 phenylhydrazine과의 반응에서 phenyl기에 결합된 치환기의 효과를 검토하였다.

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${\beta}-({\alpha}$-Benzenesulfonamidobenzal)hydrazine 및 그 유도체의 합성 (Synthesis of ${\beta}-({\alpha}$-Benzenesulfonamidobenzal)hydrazine and Its Derivatives)

  • 김태린;허태성;한인섭;백연옥
    • 대한화학회지
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    • 제23권5호
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    • pp.307-313
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    • 1979
  • N-Aryllsufonylbenzimidoyl chloride를 출발물질로 사용하여 다음과 같은 7가지 새로운 히드라진 유도체들을 합성하였다. ${\beta}-({\alpha}-Benzenesulfonamidobenzal)hydrazine\;(II),\;{\beta}-({\alpha}-Benzenesulfonamidobenzal)dimethylmethylenehydrazine\;(III),\;{\beta}-({\alpha}-Benzenesulfonamidobenzal)phenylhydrazine\;(VII),\;{\beta}-({\alpha}-Benzenesulfonamidobenzal)-4-nitrophenylhydrazine\;(VIII),\;{\beta}-({\alpha}-Benzenesulfonamidobenzal)-2,4-dinitrophenylhydrazine\;(IX),\;{\beta}-({\alpha}-Benzenesulfonamidobenzal)dimethylhydrazine\;(X),\;{\beta}-({\alpha}-Benzenesulfonamidobenzal)-p-methylphenylhydrazine\;(XI)$ 이 유도체들의 구조를 원소분석, ir, nmr, mass 스펙트럼 및 기타 화학적인 방법을 통해서 확인하였다. 일반적으로 이 치환반응은 극성인 용매에서, 그리고 친핵체인 페닐히드라진 유도체에 전자를 끄는기가 있을 때 수득율이 높았다.

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