• 제목/요약/키워드: Blood toxicity

검색결과 711건 처리시간 0.033초

Isonicotinic Acid Hydrazid (INH)의 불활성화(不活性化)에 관한 연구(硏究) (The Inactivation of Isonicotinic Acid Hydrazid (INH))

  • 김재백
    • Journal of Pharmaceutical Investigation
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    • 제9권3호
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    • pp.1-8
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    • 1979
  • The main route of metabolism of isonicotinic acid hydrazid (INH) in man is its conjugation with acetyl coenzyme A to form acetyl-INH. The reaction is catalyzed by an N-acetyl transferase in the liver. The acetylated drug can be excreted by the kidney more efficiently than INH, and the biological half-life of the drug in the body depends upon how rapidly the drug can be acetylated. This report measured the concentration of INH in the blood of 147 individuals 6 hours after they received a standard dose (9.8mg/kg) and plotted the data as a frequeney distribution hiotogram. There was bimodality, with a mean for one subpopulation at approximately $0.6{\sim}0.8\;mcg/ml.$, and a mean for the other subpopulation between 2.8 and 4.0mcg/ml. As might be expected slow acetylators of INH are more likely to develop a cumulative toxicity to the drug. The principle ,toxicity to INH is a peripheral neuritis but this adverse effect can be prevented by given extra pyridoxin to the patients, and the vitamin does not alter the antitubercular activity of INH. This report carried out that pyridoxine does not alter the ratio of free INH to the total INH in blood.

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KH-19의 5-flurouracil 부작용 억제 효력 및 기전 연구 (Studies on medicinal protection with KH-19 against side effect of 5-fIurouracil and its mechanism)

  • 양동식;성현제;윤유식
    • 한국한의학연구원논문집
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    • 제9권1호
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    • pp.137-144
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    • 2003
  • The objective on this study was to investigate medicinal protection with KH-19, which was composed of 9 kinds of oriental herbs tonifying the blood, against side effect of chemotherapy in mice and its mechanism through microarray. Not only WBC (white blood cell), and PLT (platelet) as a hematopoiesis toxicity indicator but also spleen weight as an immune toxicity indicator was reduced significantly 7 day after. 5-flurouracil (FU) treatment. However, reduction of WBC, PLT, and spleen weight after 5-FU treatment was significantly recovered by KH-19. For mechanic study on KH-19 action, gene expression in mouse spleen treated 5-FU was compared with gene expression in mouse treated 5-FU and KH-19. The result indicates that 23 genes were increased. in expression level over 2 fold and 41 genes were decreased in expression level more than 2 fold at mouse spleen by KH-19 treatment. KH-19 mechanism may be complicated more than other drug which of mechanism were composed of single compound because KH-19 was composed of various compounds.

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자동산화 Methyl Linoleate가 Mouse혈청의 효소활성에 미치는 영향 (급성 독성) (The Effect of Autoxidized Methyl Linoleate on the Serum Enzyme Activity in the Mouse (Acute Toxicity))

  • 백태홍;정낙승
    • 한국응용과학기술학회지
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    • 제1권1호
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    • pp.23-31
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    • 1984
  • In order to investigate the acute toxicity of autoxidized methyl linoleate(AOML) on the activity of serum enzymes in the mouse, we administered once 0.45ml of AOML to ICR strain mouse by using stomach tube. The following results were obtained: The total lactic dehydrogenase(LDH) activities in the serum of AOML group were generally increased than those of normal group. According to electrophoresis, the activities of LDH, were increased while those of LDH, were decreased. The activities of glutamic oxaloacetic transaminase(GOT), glutamic-pyruvic transaminase(GPT) and ${\alpha}-amylase$ in the serum of AOML group were increased more than those of normal group. The activities of alkaline phosphatase in the serum of AOML group were increased but those of isozyme were not confirmed in the normal and AOML group. In the serum protein of AOML group, albumin was increased, on the other hand ${\gamma}-globulin$ was decreased. At the peripheral blood slide smear, lymphocytes were significantly decreased but neutrophils were increased and the morphological change of erythrocytes was observed. From these results we conclude that the AOML fed to mouse influences on the activity of various serum enzymes and blood cells in the mouse.

Polychlorinated biphenyls 중독 해독제의 개발에 관한 연구 (Studies on the Development of Detoxicating Agents of Polychlorinated biphenyls Toxicity)

  • 정기화;장판섭
    • 한국식품위생안전성학회지
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    • 제2권2호
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    • pp.51-56
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    • 1987
  • PCBs 투여로 중독된 rat에 대한 천문동, 황정, 백복령, 인삼, 오가피 등의 ethanol 추출물의 효과는 다음과 같다. 1. 생약추출물의 병용투여로 PCBs 중독으로 감소된 체중이 증가하였으나 간장중량의 현저한 회복효과는 볼 수 없었다. 2. 생약추출물을 병용투여함으로써 PCBs 중독으로 감소된 RBC, WBC, Hgb 및 Het의 값이 상승하였으며 특히 백복령과 인삼 추출물의 경우 회복효과가 컸다. 3. PCBs로 증가된 혈청중 cholesterol치와 total lipids가 생약추출물을 투여함으로써 감소되었다. 4. PCBs 투여로 증가된 혈청중 GOT, GPT 및 ALP의 활성도 생약추출물의 투여로 정상치에 가깝게 감소되었다.

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Glucose가 alloxan 독성(毒性) 및 alloxan 투여가토(投與家兎)의 간대사(肝代謝)에 미치는 영향(影響)에 대(對)하여 (Influences of glucose on the alloxan toxicity to the mice and on the metabolism of the rabbits treated with alloxan)

  • 김형진;박재헌;김규호;임한영
    • 대한약리학회지
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    • 제5권1호
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    • pp.45-50
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    • 1969
  • Alloxan is a well known diabetogenic agent which destroys the beta-cell of the Langerhan's islet. The authors investigated the influence of the repeated infusion of glucose solution upon the toxicity of alloxan in the mice. The effects of glucose on the blood sugar content and the serum transaminase (S-GOT and S-GPT) activities in the rabbits treated with alloxan were also observed. The results were as follows: 1. The $LD_{50}$ of alloxan in mice showed a slight decrease by pretreatment with glucose for one or two weeks. 2. The elevated blood sugar level in rabbits induced by alloxan shelved a significant fall for the first 3 days by pretreatment with glucose. 3. The increased serum transaminase activities in rabbits induced by alloxan decreased for the first 3 days by pretreatment with glucose.

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수종 생약 수증기 증류물이 유기인제 농약에 의하여 저해된 Acetylcholinesterase 활성에 미치는 효과 (Effect of Steram Distillate from Some Medicinal Plants on Acetylcholinesterase Activity Following Intoxication by Organophosphate Pesticides in Animals)

  • 신국현;이은방;송영진;김운자
    • 생약학회지
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    • 제23권2호
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    • pp.106-114
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    • 1992
  • The acute toxicity and the effect of steam distillate obtained from several plant mixtures (G-3) on the reactivation of brain, lung, and blood acetylcholinesterase (AChE) activity, and recovery from other toxic symptoms following intoxication by organophosphate pesticides were investigated in mice and mudfish. Administration of G-3 $(50{\sim}100\;ml/kg,\;i.p.)$ immediately or 30 min prior to Diazinon or Sumithion treatments, respectively, resulted in a significant reactivation of AChE activity in brain, lung, and blood, their potencies being almost equipotent to those of 2-PAM, one of well-known antidotes. G-3 itself exhibited almost no acute toxicity even at the highest dose employed, and without effect on the inhibition of hepatic drug metabolism function following organophosphate administrations. G-3 showed a significant diminution of the death rate in mudfish as well as in mice intoxicated by Diazinon.

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Comparative In Vitro Toxicity Study of Docetaxel and Nanoxel, a Docetaxel-Loaded Micellar Formulation Using Cultured and Blood Cells

  • Do, Van Quan;Park, Kwang-Hoon;Park, Jung-Min;Lee, Moo-Yeol
    • Toxicological Research
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    • 제35권2호
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    • pp.201-207
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    • 2019
  • Nanoxel-$PM^{TM}$ (Nanoxel) is a docetaxel-loaded methoxy-poly(ethylene glycol)-block-poly(D,L-lactide) (mPEG-PDLLA). This newly developed and marketed nanoformulation exhibits an improved pharmacokinetic profile, efficacy, and safety. Although the safety of Nanoxel to docetaxel as well as its bioequivalence must be clinically confirmed, all biological activities have not been examined in in vitro or in vivo studies. Here, the toxicity in a cultured cell system and the effects on blood cells were tested with Nanoxel and docetaxel. The in vitro cytotoxicity of Nanoxel was found to be comparable to or slightly lower than that of docetaxel depending on the concentrations tested or the cell types. Neither docetaxel nor Nanoxel induced erythrocytes hemolysis and produced reactive oxygen species up to $100{\mu}M$. However, Nanoxel was able to enhance the aggregatory response of platelets to collagen, whereas docetaxel attenuated such aggregation in a range of $50-100{\mu}M$, while thrombin-induced aggregation was not affected by either of them. Docetaxel or Nanoxel did not alter basal level of $Ca^{2+}$ and 5-hydroxytryptamine-evoked $Ca^{2+}$ transient in vascular smooth muscle cells. These results suggest that the mPEG-PDLLA micellar formulation alters the toxicological properties of docetaxel, and that extra cautions are needed when evaluating the safety of nanomedicine.

표고버섯의 항산화능과 알코올분해능에 미치는 영향 (Antioxidant Activities and the Effect of Reducing Serum Alcohol Concentration of Lentinus edodes)

  • 김재현;정종길
    • 대한본초학회지
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    • 제24권4호
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    • pp.159-164
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    • 2009
  • Objectives : The purpose of this study is to evaluate antioxidant activities and reducing serum alcohol concentration of extract of Lentinus edodes on the alcohol administered rats. Methods : Antioxidant effect was measured by total phenolic compound and DPPH-radical scavenging activity of extract of Lentinus edodes in vitro. Blood alcohol concentration, aldehyde concentration, malondialdehyde concentration, glutathion concentration were measured in vivo. Results : The extract of Lentinus edodes increased DPPH-radical scavenging activity dose-dependently. The water extract with boiling water showed lower antioxidant activity and phenolic content than 70% ethanol extract in vitro. Blood alcohol concentration was significantly reduced by pre-treatment of ethanol extract of Lentinus edodes. The effect was more significant than commercial product used as a positive control. Conclusions : This study suggest that Lentinus edodes can be a potential nature resource for the management of ethanol toxicity although the mechanism of action involved in the treatment remains to be explored.

Studies on the Hypoglycemic Effect of Ginseng Polypeptide

  • Wang, B.X;Yang, M.;Jin, Y.L.;Cui, X.Y.;Wang, Y.
    • 고려인삼학회:학술대회논문집
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    • 고려인삼학회 1990년도 Proceedings of International Symposium on Korean Ginseng, 1990, Seoul, Korea
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    • pp.196-200
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    • 1990
  • the ginseng polypeptide (GPP) isolated from the root of Panax ginseng C.A. Meyer was demonstrated to decrease the levels of blood sugar and hepatic glycogen when injected intravenously to rats at a doses of 50-200mg/kg without affecting blood total lipid. When mice were injected subcutaneously daily at a dose of 50 and 100mg/kg for 7 successive days, GPP was also found to decreased blood sugar and hepatic glycoge. In addition, GPP was found to decrease various experimenta hyperglycemias induced by injection of adrenaline, glucose and alloxan. GPP exhibited inhibiting effect on the glycogen enhancement induced by glucose, but strengthening effect on the glycogen decrease induced by adrenaline. When the levels of blood total lipid and liver glycogen were increased by alloxan, GPP was shown to inhibit these changes except its lowering blood sugar. the toxicity of GPP is very low, its LD50 was found to be 1.62$\pm$0.130 g/kg for iv.

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