海南槌果藤叶提取物的抗氧化及抑菌活性研究

为了评价药用植物海南槌果藤的抗氧化活性及抑菌活性,本实验通过气相色谱与质谱联用技术(Gas chromatography-mass spectrometry,GC-MS)分析鉴定了海南槌果藤叶片甲醇提取物的化学成分,采用紫外-可见分光光度法测定了海南槌果藤甲醇提取物的总多酚、总黄酮含量、DPPH自由基、ABTS自由基、羟基自由基和超氧阴离子的清除作用;以及槌果藤氯仿相萃取物对三种食源性致病细菌和六种植物病原真菌的抑制作用。实验结果表明:海南槌果藤叶片甲醇提取物中含量最多的是酯类(45.03%)和杂环类(33.74%),其中丁基-4-庚烷基-邻苯二甲酸酯(20.58%)为主要的单组分物质。海南槌果藤甲醇提取物中总多酚含量为1.93%,总黄酮含量为2.3%;进一步研究表明海南槌果藤甲醇提取物对DPPH自由基和ABTS自由基有一定的清除能力,其IC50分别为0.454 mg/m L和0.297 mg/m L;而对羟基自由基和超氧阴离子有较强的清除能力,IC50分别为0.937、2.261 mg/m L,分别比芦丁和TBHQ标准品低。除此之外,海南槌果藤氯仿相萃取物对三种食源性致病细菌和六种植物病原真菌均有一定的抑制作用,其中对革兰氏阴性菌(大肠杆菌和铜绿假单胞菌)抑制效果较明显;同时对葡萄溃疡病菌抑制作用最强,抑制率为43.97%,其次是新暗色柱节孢,抑制率为37.5%。     

西瓜藤提取物的抑菌作用研究

采用琼脂稀释法研究西瓜藤提取物的体外抑菌作用,用小鼠腹腔注射金黄色葡萄球菌法研究80%醇提物的体内抑菌作用。结果表明:西瓜藤提取物对金黄色葡萄球菌、大肠埃希氏菌、铜绿假单胞菌、伤寒沙门氏菌、枯草芽孢杆菌和肺炎克雷伯氏菌均有不同程度的抑制作用,但对链球菌作用不明显。其中80%醇提取物和乙酸乙酯萃取物抑制金黄色葡萄球菌活性最好,其最低抑菌浓度(MIC)分别为4.2、8.4mg.mL-1。体内实验也表明,乙醇提取物具有较好的抑菌作用。西瓜藤提取物具有抑菌活性,在抑菌方面有一定开发前景。     

蓖麻提取物对鼠抗生育作用的实验研究

利用蓖麻提取物对昆明种小鼠进行了短期与长期的抗生育实验,研究发现蓖麻提取物（蓖麻油和蓖麻蛋白）对小鼠有明显的抗生育作用。蓖麻蚩白及其与蓖麻油的混合物在抗早孕方面的效果均可达到100％,蓖麻油抗着床的效果也可达到100％。蓖麻油长期抗鼠生育效果明显,在210d（正常小鼠的妊娠期是21～23d）内有效降低小鼠生育代数与产仔数,生育抑制率达80％以上。蓖麻提取物对离体小鼠子宫的影响也非常显著,通过增强小鼠子宫内部收缩有效减少着床机率。在中止妊娠的实验中发现,服用了蓖麻蛋白及其与蓖麻油的混合物的小鼠子宫内没有着床位点。     

蕲蛇提取物抗炎镇痛药理作用的研究

目的 研究蕲蛇提取物的抗炎及镇痛作用,为蕲蛇的临床应用提供科学依据.方法 采用热板法、冰醋酸刺激致痛法研究蕲蛇提取物对小鼠痛阈的影响,利用二甲苯致小鼠耳廓炎症模型和腹腔染料渗出法测定蕲蛇提取物的抗炎作用.结果 蕲蛇提取物醇溶性和水溶性部位对小鼠热板及冰醋酸致痛反应有明显镇痛作用,对二甲苯致小鼠耳廓肿胀、冰醋酸致腹腔毛细血管通透性增高均有明显的抑制作用.结论 蕲蛇提取物醇溶性和水溶性部位有一定的抗炎及镇痛作用,并且水溶性部位较醇溶性部位的药效好,可为蕲蛇的临床应用提供指导作用.     

灵芝发酵液酸性醇提物抗慢性支气管炎疗效的研究

通过灵芝发酵液酸性醇提物对小鼠的镇咳、祛痰实验,及烟熏小鼠肺部组织的形态学观察,研究灵芝酸性醇提物抗慢性支气管炎的疗效。灵芝发酵全液,不同剂量的灵芝酸乙醇提取物、灵芝酸正丁醇提取物均能显著延长二氧化硫诱发的小鼠咳嗽潜伏期,并显著抑制小鼠咳嗽次数,有明显的镇咳作用。60mg/kg给药量的正丁醇提取物使小鼠气道酚红排泄量较对照组提高了50.7%,祛痰疗效也明显优于双黄连口服液。肺组织切片病理检查表明,灵芝酸性提取物明显减轻烟熏小鼠的气管、支气管粘膜损伤,慢性支气管炎的组织病理学变化明显轻于单纯烟熏模型组,且抗炎、抗损伤作用与双黄连相当,这可为灵芝酸产品的研究开发提供一定的药理依据。     

花椒总生物碱镇痛、抗炎、止痒作用研究

目的:研究花椒生物碱镇痛、抗炎及止痒作用。方法:分别采用热板法考察其镇痛作用二甲苯致炎法考察其抗炎作用、低分子右旋糖酐-40诱发小鼠皮肤瘙痒研究其止痒作用。结果:中、高浓度的花椒生物碱对小鼠热刺激引起的疼痛具有较强的镇痛作用;高浓度的花椒生物碱能较强抑制二甲苯所致小鼠耳肿胀,并能缓解分子右旋糖酐-40诱发的小鼠皮肤瘙痒。具有较强的抗炎、止痒作用。结论:花椒生物碱具有较强的镇痛、抗炎、止痒作用。     

灵芝子实体醇提取物的毒理研究

本文主要研究灵芝子实体醇提物的毒理学并评价其安全性,利用小鼠急性毒性试验和遗传毒性试验(Ames试验、小鼠骨髓细胞微核试验、小鼠精子畸形试验)对灵芝醇提物的毒性进行考察。试验结果显示,小鼠对灵芝醇提取物的最大耐受量是15 000mg/(kg?bw);灵芝醇提取物在有或无S9的条件下,对鼠伤寒沙门氏菌的突变型菌株TA97、TA98、TA100及TA102均无潜在致突变性;灵芝醇提取物在小鼠骨髓细胞微核试验和小鼠精子畸形试验中均呈阴性反应,不同剂量的样品组与阴性对照组之间无显著性差异。该结果表明灵芝醇提取物基本无毒性,属实际无毒物质。本研究为灵芝醇提取物的产品开发和应用提供了科学研究。     

杨梅果实提取物抗小鼠腹泻作用的研究

目的研究杨梅果实提取物的抗小鼠腹泻作用,包括预防和治疗作用。方法给小鼠腹腔注射甲型副伤寒沙门菌造成急性腹泻模型,经口灌胃杨梅果实提取物溶液,通过腹泻次数研究提取物对小鼠腹泻的预防作用;先灌胃杨梅果实提取物溶液再给小鼠注射菌液致泻,记录腹泻次数以研究提取物对小鼠腹泻的治疗作用。结果灌胃杨梅果实提取物的小鼠的腹泻次数均有明显的下降,且醇提物的作用效果要好于水提物。结论杨梅果实提取物对甲型副伤寒沙门菌引起的小鼠腹泻具有一定的预防和治疗作用。     

保护风蚀地的刺山柑

刺山柑(Capparis spinosa),又称老鼠瓜、野西瓜、槌果藤、瓜儿菜或抗旱草等,属山柑科或白花菜科,藤本蔓生小半灌木,株高30—50厘米,植丛冠幅4—16(25)平方米,根深粗壮,有的根垂直向下可延伸达30—40米。主茎不明显,枝丛生,平铺地面或斜向升高,长达2—3     

植物寄生线虫在我国的危害特点

早在1743年Needham第一次报道线虫能寄生小麦引起粒瘿病。1850年Hardy在野燕麦上发现有另一种寄生线虫。1859年Schacht报道了寄生甜菜的线虫,1871年Schmidt对这线虫进行描述,命名为甜菜孢囊线虫(Heterodera sckachtii)。后来又有许多学者继续报道了许多植物寄生线虫,才逐渐引起人们的注意。到1906年以后便形成一门专业学科,近三十年来更进一步得到飞速发展。迄今全世界共计发现并正式描述报道的植物寄生线虫已达140多属、2000多种。 我国的植物寄生线虫研究工作起步也早,最初是1916年章祖纯在北京发现小麦线虫引起粒瘿病。50年代便在河北、天津、北京、山东     

Evaluation of antifertility potential of Piper betle (Petiole) on female wistar rats “rising approaches of herbal contraception’’

Piper betle (Petiole) is used of herbal methods for fertility regulation is widely accepted alternative for the synthetic drugs containing chemical having side effects. Piper betle (Petiole) is the plant having several medical properties but no reports were available on the antifertility activity. The aim of this study was to investigate the antifertility activity of extracts of Piper betle (Petiole) on female wistar rats at the doses 500 mg/kg b.wt./day for 30 days. Different parameters were studied in female wistar rats including effect of Reproductive outcome, Anti-implantation, Abortifacient and Estrogenic & Anti-estrogenic activity, were observed. Piper betle shown positive test for Alkaloids, Steroid, Flavonoids, Terpene, Carbohydrates and Tannin. The extract has anti-fertility effect the control rats showed good number of litters and treatment of animal with different extracts resulted a significant (P < 0.05, P < 0.01). Antifertility activity 51% and 37.2% was exhibited by Alcoholic extracts of Piper betle (Petiole) APB and Aqueous extracts of Piper betle (Petiole) WPB respectively. After 21 days of the extracts free period, the antifertility effect of the extracts was reversed. The extract treatment with APB, an increase in the percentage of resorption index indicates the failure in development of embryo. The mean percentage of anti-implantation and abortifacient were found to be highest for APB-38.45%, WPB 13.62, and APB-28.96%, WPB-12.75% respectively. The decrement in implantation caused by the extracts may be due to estrogenic or anti-estrogenic activity. However, along with standard APB exhibiting more potent estrogenic and less potent anti-estrogenic when compared with standard. Female antifertility agents should include acceptability, safety and efficacy during and after the treatment. The above results revealed the potential, reversible female antifertility effect of alcoholic extract Piper betle (Petiole).     

Inhibition of the metabolism of ram spermatozoa by derivatives of α-chlorohydrin

The effects of the male antifertility agent, α-chlorohydrin, six of its derivatives, and glycidol were studied on the metabolism of washed ram spermatozoa in vitro with fructose as substrate. The α-chlorohydrin derivatives were the amino, the phosphorylated, and four glycol-bridge (ketal) compounds. All compounds except glycidol, in a concentration between 0.1 and 100 mM, reduced the aerobic glycolsis and/or oxidation of fructose. However, there was not a high correlation between the ability of these compounds to inhibit the metabolism of ram spermatozoa in vitro and their antifertility activity when administered to male rats. Other factors are clearly involved in their antifertility activity, eg, the concentration of the compounds in the epididymis and their conversion of either more or less spermicidal compounds in the body.     

The effect of the isomers of α-chlorohydrin and racemic β-chlorolactate on the rat kidney

The (R)- and (S)-isomers of the male antifertility agent α-chlorohydrin have been synthesized. When administered to rats, the (R)-isomer induced a period of diuresis and glucosuria, whereas the (S)-isomer, which possesses the antifertility activity, had no detrimental action on the kidney. Neither of the isomers of α-chlorohydrin nor those of an active analogue, 3-amino-1-chloropropan-2-ol, had any inhibitory activity on the oxidative metabolism of glucose or lactate in isolated kidney tubules. However, β-chlorolactate, a metabolite common to both compounds, inhibited the oxidation of glucose, lactate, pyruvate and glutamate to CO₂. It is proposed that the antifertility action of the (S)-isomers of α-chlorohydrin and 3-amino-1-chloropropan-2-ol is unrelated to the renal toxicity of the (R)-isomers, a toxic action involving the inhibition of oxidative metabolism by (S)-β-chlorolactate or a further product of this metabolite.     

Effect of intravaginal instillation of some non-steroidal oral antifertility agents on pregnancy in rats

A study was conducted of the effect of intravaginal instillation of 3 nonsteroidal oran antifertility agents in pregnant rats. The 3 compounds used were 2-phenyl-3-rho-beta-pyrrolidinoethoxyphenyl-6-methox y benzofuran hydrochoride (DBF), 20 mg/kg; 2-phenyl-3-rho-beta-pyrrolidi noethoxyphenyl-naptha (2:1,b furan (NF), 10 mg/kg; and Centchroman, 1.25 mg/kg. These agents were administered on Day 1 postcoitum at the single-day oral contraceptive dose. Control animals were inserted with a pellet containing only carboxymethyl cellulose. Only Centchroman was 100% effective in preventing pregnancy. Even at half the normal dose, Centchroman was effective. Of the 3 compounds, only Centchroman has an antiprogestational property which may be contributing to Centchroman's high antifertility activity by the vaginal route and may prevent side effects.     

棉酚对鼠类生精细胞LDH-X活性的影响

本文测定了连续饲喂棉酚达6周的大鼠和小鼠的生精细胞的LDH-X活性。结果表明,棉酚能够明显地抑制大鼠成熟精子的LDH-X活性;而对睾丸LDH-X活性的抑制,与对照相比,无显著性差异。在小鼠中,未发现棉酚对成熟精子及睾丸生精细胞中的LDH-X活性产生具统计学意义的抑制作用。本文结合精子发生过程及LDH-X的特殊功能,对棉酚抗生育作用的可能机理进行了讨论。     

Abortifacient effects of Vibrio cholerae exo-enterotoxin and endotoxin in mice.

To study antifertility properties of microbial toxins, exoenterotoxin and endotoxin from Vibrio cholerae were injected intravenously into mice at different times during pregnancy. The two substances induced termination of pregnancy, but the patterns of abortifacient activity were different. Exotoxin terminated pregnancy in mice when administered between Days 4 and 10 of gestation, but abortifacient activity was reduced in animals more than 10 days pregnant; exogenous progesterone did not protect the pregnancies. Endotoxin was most effective in terminating pregnancy when injected after mid-gestation and the active principle was heat-stable; exogenous progesterone was not able to prevent the effects of endotoxin. Animals treated with endotoxin on Day 17 often gave birth to live young prematurely; indomethacin reduced the incidence of premature littering. The results demonstrate that exo- and endotoxins have antifertility properties and both appear to act on intrauterine targets rather than inducing progestin deficiency.     

九里香蛋白多糖的抗生育及其它生物活性

九里香蛋白多糖有明显的抗生育作用,小鼠腹腔注射剂量2.08mg/kg,抗早孕率达72—83％。能增强小鼠腹腔巨噬细胞的吞噬功能,吞噬指数和吞噬百分数分别为对照组的5.42和1.70倍。能增加致敏动物血清中溶血素含量,小鼠HC_(50)为对照组的5.1倍。对大鼠新鲜红细胞有明显的促进凝集作用,凝集率为31.1％。能对抗环磷酰胺引起的白细胞减少,对照组和九里香蛋白多糖组白细胞下降率分别为42.7％和26.7％。对二甲苯所致小鼠耳部炎症也有对抗作用,抑制率达52％。有抗凝血作用,家兔静脉注射18mg/kg,凝血时间延长1.76分钟。毒性较低,小鼠腹腔注射LD_(50)为462±56.7mg/kg。     

Antifertility activity and toxicity of alpha-chlorohydrin aromatic ketal analogues in male rats

The antifertility activity and toxicity of alpha-chlorohydrin and seven aromatic ketal derivatives were investigated in male rats. At a dose of 5 mg/kg injected intraperitoneally each day for 14 days, alpha-chlorohydrin and the methoxy benzaldehyde derivative (compound 2) produced complete infertility. The benzaldehyde derivative (compound 1) was 89% effective and the other five compounds 71-25% effective. All compounds except the least effective antifertility agent, the methylbenzaldehyde derivative (compound 3), reduced the motility of sperm recovered from the epididymis. None of the compounds caused a decrease in body or testes weight but some increased adrenal weight.     

Structural requirements of some sulphonamides that possess an antifertility activity in male rats

Sulphonamides with different chemical structures were synthesized and these 13 compounds together with 7 commercially available sulpha drugs were tested for antifertility activity by natural mating in male rats. All compounds were given daily by gastric intubation at doses of 125, 150, 250 or 450 mg/kg for 6 weeks. Sulphapyridine caused a dose-related and reversible reduction in fertility at doses between 125 and 450 mg/kg. At the high dose, fertility was reduced to 25.9% of control at 5 weeks after treatment, and complete recovery occurred by 3 weeks after drug withdrawal. This activity was abolished when the pyridine ring was substituted by other heterocyclic rings, except sulphachloropyridazine which had only weak activity. Replacement of the pyridine ring by a hydrogen atom or short aliphatic chains preserved or even enhanced the potency. Thus, sulphanilamide, N1-methylsulphanilamide or N1-diethylsulphanilamide produced a marked but reversible reduction in fertility. Removal or substitution of the N4-amino group on the benzene ring of sulphapyridine with a methyl group destroyed the activity. However, the bromo or nitro analogue (at the para- but not the meta-position of the benzene ring) still possessed some activity. N4-Acetyl derivatives of sulphapyridine, sulphanilamide, and N1-diethylsulphanilamide were as potent as their parent compounds. These results suggest that the presence of pyridine or other heterocyclic rings is not necessary for the antifertility activity of sulphonamide compounds. However, the N4-amino group is indispensable. In addition, acetylation of this amino group does not change the potency. The prototype of the antifertility sulphonamides therefore seems to be sulphanilamide.     

Ultrastructural, fertility, and spermicidal studies with isomers and derivatives of gossypol in male hamsters

The effects of fourteen new, orally administered synthetic analogs of gossypol on testicular ultrastructure and fertility in hamsters and the spermicidal properties of these compounds, as well as of the optical isomers of gossypol against hamster and human sperm in vitro, are reported in this study. Test compounds were administered to adult male hamsters by daily gavage for 9 weeks at doses ranging from 15 to 50 mg/kg. The results of this study have demonstrated that the fourteen new gossypol analogs evaluated herein are not effective as male antifertility agents and their in vitro activity or lack of activity as spermicides is unrelated to their in vivo contraceptive potential. In addition, the results of the study suggest that (1) the isopropyl moiety of the gossypol molecule, like the aldehyde group, is essential for its mechanism of action and (2) the pathognomonic defect in the mitochondrial sheath induced by gossypol appears to be related to its unique activity as a male antifertility agent. The significance of these findings is discussed.