壳聚糖包衣对油菜种子萌发及幼苗耐盐性影响

以不同浓度的壳聚糖对油菜种子进行包衣处理,考察其对油菜种子萌发及幼苗耐盐性的影响,并在不同盐浓度胁迫条件下对种子萌发时的发芽势、发芽率、生物量（鲜重、干重、根长、芽长）等指标进行测定,同时分析油菜幼苗叶绿素含量、可溶性蛋白及可溶性糖含量的变化。结果表明,一定浓度的壳聚糖包衣处理可提高油菜种子发芽率、发芽势、生物量、幼苗的耐盐指数、叶绿素含量、可溶性蛋白及可溶性糖的含量,其中浓度为0.25 g·L^-1壳聚糖包衣处理对油菜种子萌发的促进效果较好,而浓度为0.50 g·L^-1壳聚糖包衣处理对提高油菜幼苗耐盐性具有较好的促进作用。     

薯蓣皂素对小麦幼苗抗旱性的影响

用不同浓度的薯蓣皂素喷施处理小麦幼苗叶片,研究薯蓣皂素在干旱胁迫下对小麦幼苗影响。结果表明,喷施一定浓度的外源薯蓣皂素,在干旱胁迫下可保持小麦幼苗叶片相对含水量,提高SOD和POD活性,降低MDA含量,对小麦幼苗抗旱有一定的作用。且薯蓣皂素最佳质量浓度为0.5 mg.L-1。     

外源甲醇对油菜种子萌发和幼苗生长的影响

以中国南、北2个主要栽培品种‘玉油二号’和‘秦油二号’油菜种子为供试材料,采用溶液培养方法研究了0~2 000mmol·L-1甲醇溶液处理下,油菜种子萌发、幼苗生长特征及其相关生理生化指标的变化。结果表明:(1)10~1 000mmol·L-1甲醇处理的油菜种子萌发指标(发芽率、发芽势、发芽指数、活力指数)和幼苗生长指标(幼芽及幼根长度、鲜重、根冠比)均比对照显著增加,而甲醇溶液浓度为2 000mmol·L-1时油菜种子萌发和幼苗生长受到显著抑制;两个油菜品种种子萌发和幼苗生长在甲醇溶液处理下均表现为相同的变化趋势,但也存在品种的差异,‘秦油二号’生长受影响程度低于‘玉油二号’。(2)随着甲醇溶液浓度的增加,油菜种子萌发指标和幼苗生长指标表现出先增加后降低的趋势,并在甲醇溶液浓度为100mmol·L-1时均达到最大值,继续高于此浓度后促进作用即减弱以至消失,甚至产生抑制作用。(3)随着甲醇处理溶液浓度的增加,油菜幼苗叶片的叶绿素含量呈先增后降的趋势,而同期叶片的MDA和过氧化氢含量却呈先降后升的相反趋势,且均在相同的100mmol·L-1浓度下分别达到最大或者最低值。研究认为,适宜浓度的甲醇溶液能够促进油菜种子萌发和幼苗生长。     

水杨酸对菊叶薯蓣中薯蓣皂素生物合成的影响

薯蓣皂素为甾体激素药物合成起始原料,主要来源于菊叶薯蓣等薯蓣属植物的块茎或根状茎,因而关于提高菊叶薯蓣中薯蓣皂素含量的研究有重要意义。利用水杨酸处理菊叶薯蓣的离体植株,研究其对薯蓣皂素生物合成的影响及作用机制。100μmol·L－1的水杨酸处理使薯蓣皂素积累量最大,且提高了叶绿素含量和可溶性糖含量,降低可溶性蛋白含量。半定量 RT-PCR 检测基因表达发现,除了法尼基二磷酸（FPP）基因,水杨酸增强菊叶薯蓣角鲨烯合酶（SQS）基因、甲基戊二酰辅酶 A 还原酶（HMGR）基因、环阿屯醇合成酶（CAS）基因的表达。研究结果为提高菊叶薯蓣中薯蓣皂苷的含量、揭示水杨酸促进薯蓣皂素生物合成的机制等研究提供了基础。     

外源5-氨基乙酰丙酸对盐胁迫下菘蓝种子萌发及幼苗抗氧化酶活性的影响

采用砂培方式,研究了外源5-氨基乙酰丙酸(ALA)对盐胁迫下菘蓝种子的萌发、幼苗叶片的可溶性糖含量、丙二醛(MDA)含量及其抗氧化酶活性的影响,探讨ALA缓解菘蓝受盐胁迫伤害的响应机制。结果显示:(1)菘蓝种子萌发及幼苗生长在100 mmol·L^-1 NaCl胁迫下受到明显的抑制,种子发芽率、发芽势、发芽指数、活力指数与自然含水量均显著降低,丙二醛含量、可溶性糖含量以及超氧化物歧化酶(SOD)、过氧化物酶(POD)活性显著升高。(2)盐胁迫下适宜浓度的ALA处理显著提高了种子萌发率、自然含水量及SOD、POD和CAT活性,降低了可溶性糖和丙二醛的含量,并以16.7 mg·L^-1 ALA处理盐胁迫下菘蓝种子的发芽率、发芽势最大,其幼苗的SOD、POD、CAT活性最强。研究表明,盐胁迫显著抑制菘蓝种子的萌发及幼苗生长,适宜浓度的ALA能够有效缓解盐胁迫对菘蓝种子萌发及幼苗生长的伤害,提高植株的抗盐性,并以16.7 mg·L^-1 ALA处理效果最佳。     

链带藻源生物刺激剂提高小麦对盐胁迫的生理适应

盐胁迫是影响小麦萌发、生长和生产的最重要环境因素。探究链带藻（Desmodesmus Sp.）生物刺激剂对盐胁迫条件下小麦种子和早期幼苗抗盐、生长和生理的缓解效应以及最佳施用浓度,可为其应用于缓解小麦盐胁迫影响提供理论依据。【方法】通过室内培养皿培养法,将小麦种子置于100 mmol/L NaCl胁迫下,外源添加25,50,100,200 mg/L的链带藻提取物（DAE）,处理7 d后测量各项萌发和生长参数。【结果】外源添加DAE处理缓解了盐胁迫对小麦种子萌发和早期幼苗生长的抑制作用,提高了盐胁迫下小麦种子的萌发率和叶片含水量,促进了生物量的积累;提高了幼苗叶片超氧化物歧化酶、过氧化物酶、过氧化氢酶、抗坏血酸过氧化物酶活性以及脯氨酸、可溶性总糖、可溶性蛋白质和叶绿素的含量;降低了脂质过氧化作用,减少了丙二醛含量和膜透性。在100 mmol/L NaCl胁迫条件下,25 mg/L DAE对盐胁迫下小麦种子萌发及早期幼苗生长抑制作用的缓解效果最佳。【结论】链带藻细胞提取物通过促进小麦种子早期萌发的启动,提高小麦幼苗叶绿素含量、抗氧化酶活性和渗透调节能力,增强小麦种子及早期幼苗对盐胁迫的适应性,提升了小麦的耐盐能力。     

臭氧水浸种对黄瓜种子萌发及幼苗生长的影响

臭氧水处理10、30和50 min后的黄瓜种子,种子萌发及幼苗生长均受到促进,种子的发芽率和活力指数、萌发种子的过氧化氢酶(CAT)和淀粉酶的活性以及呼吸速率、幼苗的壮苗指数和根系活力均有提高;处理70和90min的黄瓜种子萌发和生长则受到抑制,种子电解质外渗,过氧化氢酶和淀粉酶活性下降.     

壳聚糖包衣对油菜种子萌发和幼苗生长以及几个生理生化指标的影响

不同酸溶剂与不同分子量壳聚糖包衣均促进油菜种子萌发和幼苗生长。其中壳聚糖无机酸溶剂包衣种子发芽率及幼苗生化等指标优于有机酸溶剂 ;小分子量壳聚糖包衣优于大、中分子量的。壳聚糖包衣处理有促进植物生长之功能     

不同处理对黄精种子萌发和幼苗生长的影响

目的：探究不同处理对黄精种子萌发和幼苗生长的影响，完善黄精种子有性繁育技术体系。方法：采用不同pH值的缓冲溶液、不同外源激素溶液和不同种子包衣剂，分别处理黄精种子，综合测定分析各处理对黄精种子萌发和幼苗生长影响。结果：酸性环境pH(4～6)中黄精种子的发芽势、发芽率、初生小球茎直径、须根数均高于碱性环境pH(8～10)。不同外源激素对黄精种子萌发和幼苗生长均有显著的促进作用。其中，6-BA处理组黄精种子的发芽势最高为20.00%,ABA处理组黄精种子的发芽率最高为44.00%，幼苗初生小球茎直径和须根数由高至低依次均为：ABA> 6-BA> GA₃> 2,4-D。不同包衣剂对黄精种子萌发和幼苗生长均有一定的抑制作用，其中SLS处理组对黄精种子萌发和幼苗生长的抑制作用最弱，且与CK组无显著差异(P <0.05)。综合评分表明，对黄精种子萌发和幼苗生长促进作用较强的处理组分别为：pH4处理组、ABA处理组和SLS处理组。结论：酸性土壤环境有利于黄精种子萌发和幼苗生长，100 mg/L ABA溶液可以显著促进黄精种子萌发和幼苗生长，SLS包衣剂可...     

水淹和不同贮藏方法对中华蚊母树种子萌发及其生理特征和幼苗生长活力的影响

以中华蚊母树(Distylium chinense)种子为材料,分别设置4个贮藏时间(0、30、60和90d),以及2m水淹(FSW)、低温沙藏(CSS)、低温干藏(CDS)、室温沙藏(RSS)、室温干藏(RDS)和低温层积(CSF)6个贮藏方式对种子进行贮藏实验,并测定分析各处理种子的萌发特性及其幼苗生长状况,明确不同储藏方式和时间对中华蚊母树种子萌发及幼苗生长的影响。结果表明:(1)CSF处理30d后,中华蚊母树的种子有65.37%发生霉烂,最后萌发种子数为贮藏种子的30.93%;FSW处理90d的种子的萌发率为35.67%。(2)室内贮藏90d后,CSS、CDS、RSS和RDS处理的种子萌发率较新鲜种子萌发率(26.37%)显著增大,并以4℃下CDS处理90d的种子萌发率最大(70.65%),萌发速率系数为1 956.97。(3)CDS处理90d的种子淀粉和蛋白质含量较新鲜种子分别降低了38.75%和20.16%,而可溶性糖含量增加了31.47%;FSW处理后的种子淀粉、蛋白质及可溶性糖含量均较新鲜种子显著降低,降幅分别为48.75%、62.62%和6.29%。(4)不同贮藏方式贮藏90d后,各处理间中华蚊母树幼苗的生长活力表现出显著差异,并以CDS处理的幼苗活力最高,而FSW处理的种子萌发后幼苗的活力显著低于其他贮藏方式。研究表明,低温条件下中华蚊母树种子萌发率及幼苗活力显著高于室温贮藏,可能是在低温贮藏条件下种子的贮藏物质由淀粉水解为可溶性糖,更利于种子吸收并为种子萌发提供了能量,从而加快了破除种子生理休眠的进程,而且中华蚊母树种子对水淹有一定的耐受性,故中华蚊母树可以作为三峡水库消落带高海拔区域植被恢复与重建优先考虑的物种。     

Diosgenin--a growth stimulator of mammary gland of ovariectomized mouse.

Estrogenic action of diosgenin on the mammary epithelium of ovariectomized (OVX) mouse has been reported. Diosgenin when administered (sc) at the dose levels of 20 and 40 mg/kg body weight for a period of 15 days stimulated the growth of mammary epithelium. This was indicated by the increase in DNA content, increase in number of ducts and appearance of terminal endbuds. There was a significant increase in the mammary development scores in the presence of diosgenin. Concomitant treatment of estrogen and diosgenin showed augmentation of estrogenic effect of diosgenin especially at the higher dose level (40 mg/kg body wt). Diosgenin showed a lack of progesterogenic action as was apparent from the absence of alveolar development even in the presence of exogenous estrogen.     

Effects of diosgenin on myometrial matrix metalloproteinase-2 and -9 activity and expression in ovariectomized rats

Diosgenin, a traditional Yam extraction, has been used in hormone replacement for menopausal women. We aimed to investigate the influences of diosgenin administration upon the MMP-2 and -9 activity and expression and reproductive hormones of ovariectomized (OVX) rats, a model of menopausal status. Seven-week old female Wistar rats with bilateral OVX or sham operation (controls) were divided and administered different dosages of diosgenin (0, 10, 50, or 100 mg/kg/day) for 8 weeks. Serum was then sampled for progesterone (P4) and estradiol (E2) assay and uterine horns harvested. Myometrial MMP-2 and -9 activity and expression were surveyed and myometrial collagen expression was also assayed. The results show higher body weight in OVX rats across the 8 weeks post surgery and no significant differences were noted among OVX or Sham rats with diosgenin supplements. There were lower P4 and E2 concentrations in OVX rats compared to Sham rats, and higher P4 concentration of Sham rats post diosgenin supplement. MMP-2 and -9 mRNA expression and activity was lower in OVX rats, although higher MMP-2 and lower MMP-9 activity/mRNA expression was observed in OVX rats post diosgenin supplementation. Collagen mRNA expression was higher in OVX rats compared to Sham controls, and diosgenin administration decreased collagen mRNA expression in OVX rats. In conclusion, diosgenin is associated with gelatinase expression and collagen metabolism in OVX rats. Diosgenin administration can partially reverse the effects of OVX upon MMP functions and hormone status. Adequate diosgenin supplement might modulate myometrial gelatinase expression and collagen metabolism in menopausal subjects.     

Diosgenin inhibits the migration of human breast cancer MDA-MB-231 cells by suppressing Vav2 activity

Diosgenin, a naturally occurring steroidal saponin, possess tumor therapeutic potential. However, the effect of diosgenin on cancer metastasis remains poorly understood. In this study, we performed in vitro experiments to investigate the inhibitory activity of diosgenin on human breast cancer MDA-MB-231 cell migration, and reveal the possible mechanism. Diosgenin caused a marked inhibition of cell migration in MDA-MB-231 cell by transwell assay. In addition, diosgenin significantly impacted MDA-MB-231 cell migratory behavior under real-time observation. We also found diosgenin significantly inhibited actin polymerization, Vav2 phosphorylation and Cdc42 activation, which might be, at least in part, attributed to the anti-metastatic potential of diosgenin. These findings reveal a new therapeutic potential of diosgenin for human breast cancer metastasis therapy.     

Diosgenin induces apoptosis in IGF-1-stimulated human thyrocytes through two caspase-dependent pathways

Insulin-like growth factor-1 (IGF-1) is a growth factor of the thyroid that has been shown in our previous study to possess proliferative and antiapoptotic effects in FRTL-5 cell lines through the upregulation of cyclin D and Fas-associated death domain-like interleukin-1-converting enzyme (FLICE)-inhibitory protein (FLIP). Diosgenin, a natural steroid sapogenin from plants, has been shown to induce apoptosis in many cell lines, with the exception of thyroid cells. In this report, we investigated the apoptotic effect and mechanism of diosgenin in IGF-1-stimulated primary human thyrocytes. Primary human thyrocytes were preincubated with or without IGF-1 for 24h and subsequently exposed to varying concentrations of diosgenin for different times. We found that diosgenin induced apoptosis in human thyrocytes pretreated with IGF-1 in a dose-dependent manner through the activation of caspase cascades. Moreover, diosgenin inhibited FLIP and activated caspase-8 in the FAS-related apoptotic pathway. Diosgenin increased the production of ROS, regulated the balance of Bax and Bcl-2 and cleaved caspase-9 in the mitochondrial apoptotic pathway. These results indicate that diosgenin induces apoptosis in IGF-1-stimulated primary human thyrocytes through two caspase-dependent pathways.     

盾叶薯蓣营养器官薯蓣皂甙元含量的动态变化

利用高效液相色谱(HPLC)法对盾叶薯蓣营养器官特别造根状茎中薯蓣皂甙元含量的动态变化、品种之间的差异以及雌雄株之间的差异进行了研究。结果表明:实生苗根状茎中薯蓣皂甙元的含量,2年生高于1年生;根茎营养繁殖的2年生根状茎中皂甙元的含量高于1年生的含量;花叶品种的含量高于绿叶品种的含量;雄株的含量比雌株的含量高。在地上的缠绕茎和叶中没有检测到薯蓣皂甙元。由根茎繁殖的1年生根状茎前期皂甙元含量增加缓慢,后期增加较快;2年生根状茎盛花期含量最高,开花后期含量最低,随后含量逐渐增加。为此应在花叶品种中选择产量高、抗性强的品种作为栽培品种。合适的采挖期仍以地上缠绕茎枯萎期为宜。     

盾叶薯蓣营养器官薯蓣皂甙元含量的动态变化

利用高效液相色谱(HPLC)法对盾叶薯蓣营养器官特别是根状茎中薯蓣皂甙元含量的动态变化、品种之间的差异以及雌雄株之间的差异进行了研究。结果表明：实生苗根状茎中薯蓣皂甙元的含量,2年生高于1年生;根茎营养繁殖的2年生根状茎中皂甙元的含量高于1年生的含量;花叶品种的含量高于绿叶品种的含量;雄株的含量比雌株的含量高。在地上的缠绕茎和叶中没有检测到薯蓣皂甙元。由根茎繁殖的1年生根状茎前期皂甙元含量增加缓慢,后期增加较快;2年生根状茎盛花期含量最高,开花后期含量最低,随后含量逐渐增加。为此应在花叶品种中选择产量高、抗性强的品种作为栽培品种。合适的采挖期仍以地上缠绕茎枯萎期为宜。     

Effect of diosgenin on lipid metabolism in rats.

The purpose of this study was to determine whether diosgenin suppresses cholesterol absorption in rats, and to examine relevant changes in cholesterol and bile acid metabolism. Diosgenin fed with the diet for 1 week inhibited cholesterol absorption as determined by the serum isotope ratio technique, as well as by measuring in the feces the amount of unabsorbed radioactivity from orally administered [3H]cholesterol. In addition, diosgenin suppressed the serum and liver uptake of radioactivity from co-administered [3H]cholesterol as well as the accumulation of liver cholesterol in the cholesterol-fed rat; diosgenin was substantially more active than cholestyramine or beta-sitosterol. In vitro, diosgenin had no effect on the activity of rat pancreatic esterase. Diosgenin decreased the elevated cholesterol in serum LDL and elevated cholesterol in the HDL fraction of cholesterol-fed rats; diosgenin had no effect on serum cholesterol in normocholesterolemic rats. In contrast to cholestyramine, diosgenin markedly increased neutral sterol excretion without altering bile acid excretion; in vitro, diosgenin had no effect on bile acid binding. Diosgenin treatment increased hepatic and intestinal cholesterol synthesis as well as the activity of hepatic HMG CoA reductase. This was accompanied by increased biliary concentration of cholesterol, but not of bile acids. Diosgenin had no effect on cholesterol synthesis when added to normal rat liver homogenates. It was concluded that diosgenin interferes with the absorption of cholesterol of both exogenous and endogenous origin; such interference is accompanied by derepressed, i.e., increased, rates of hepatic and intestinal cholesterol synthesis. The increased unabsorbed cholesterol together with enhanced secretion of cholesterol into bile resulted in increased excretion of neutral sterols without affecting the biliary and fecal excretion of bile acids.     

Diosgenin inhibits superoxide generation in FMLP-activated mouse neutrophils via multiple pathways

Abstract

Diosgenin possesses anti-inflammatory and anticancer properties. Activated neutrophils produce high concentrations of the superoxide anion which is involved in the pathophysiology of inflammation-related diseases and cancer. In the present study, the inhibitory effect and possible mechanisms of diosgenin on superoxide generation were investigated in mouse bone marrow neutrophils. Diosgenin potently and concentration-dependently inhibited the extracellular and intracellular superoxide anion generation in Formyl-Met-Leu-Phe (FMLP)- activated neutrophils, with IC₅₀ values of 0.50 ± 0.08 μM and 0.66 ± 0.13 μM, respectively. Such inhibition was not mediated by scavenging the superoxide anion or by a cytotoxic effect. Diosgenin inhibited the phosphorylation of p47phox and membrane translocation of p47phox and p67phox, and thus blocking the assembly of nicotinamide adenine dinucleotide phosphate oxidase. Moreover, cellular cyclic adenosine monophosphate (cAMP) levels and protein kinase A (PKA) expression were also effectively increased by diosgenin. It attenuated FMLP-induced increase of phosphorylation of cytosolic phospholipase A (cPLA₂), p21-activated kinase (PAK), Akt, p38 mitogen-activated protein kinase (p38MAPK), extracellular signal-regulated kinase (ERK1/2), and c-Jun N-terminal kinase (JNK). Our data indicate that diosgenin exhibits inhibitory effects on superoxide anion production through the blockade of cAMP, PKA, cPLA₂, PAK, Akt and MAPKs signaling pathways. The results may explain the clinical implications of diosgenin in the treatment of inflammation-related disorders.