外源亚精胺对Ca(NO3)2胁迫下黄瓜幼苗生长和活性氧代谢的影响

以温室专用黄瓜品种'津优3号'幼苗为材料,采用营养液栽培方法,研究了叶面喷施1 mmol·L-1亚精胺(Spd)对60 mmol·L-1硝酸钙胁迫下黄瓜幼苗生长和植株体内活性氧代谢的影响.结果显示,Ca(NO3)2胁迫下,黄瓜幼苗叶片和根系O-·2产生速率显著增加,超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)等抗氧化酶活性升高,同时MDA含量和相对电导率明显提高,显著降低了黄瓜幼苗的株高、鲜重和干重;外源喷施Spd提高了硝酸钙胁迫下黄瓜幼苗叶片和根系SOD、POD和CAT活性,降低了O-·2产生速率,MDA含量及相对电导率显著下降.由此可见,外源Spd可通过提高黄瓜幼苗SOD、POD和CAT等保护酶活性来增强其对体内活性氧的有效清除能力,降低膜质过氧化伤害程度,从而缓解硝酸钙胁迫对黄瓜幼苗生长的抑制.     

外源亚精胺对Ca(NO3)2胁迫下番茄幼苗合特性和抗氧化酶活性的影响

以耐盐性较弱的番茄品种上海‘合作903’幼苗为试验材料,采用营养液栽培方法,研究了叶面喷施1 mmol·L-1亚精胺( Spd)对75 mmol·L-1 Ca(NO3)2胁迫下番茄幼苗生长、叶绿素含量、光合及荧光参数、叶片抗氧化酶活性的影响,以探讨外源亚精胺缓解Ca( NO3)2胁迫伤害的机制.结果显示:Ca(NO3)2胁迫能够显著抑制番茄幼苗的生长;与Ca( NO3)2胁迫处理相比,叶面喷施外源Spd 9 d后,受胁迫番茄幼苗的株高、茎粗、干重、鲜重分别显著增加70.9％、15.8％、43.4％、41.4％;叶绿素a、b的含量分别提高17.7％、13.8％;净光合速率(Pn)、气孔导度(Gx)、蒸腾速率(T1)、光合电子传递效率(rETR)和光化学猝灭系数(qp)分别升高6.6％、18.0％、31.0％、4.9％、5.0％,而胞间二氧化碳浓度(C1)、非光化学猝灭系数(q、)分别降低21.5％、8.1％;超氧化物歧化酶(SOD)、过氧化氢酶(CAT)活性分别增加10.7％和37.5％,而丙二醛(MDA)含量和超氧阴离子(O2)产生速率分别显著下降34.5％、17.1％.研究表明,外源Spd通过提高番茄幼苗抗氧化酶活性来有效清除体内活性氧,维持光合机构的稳定性,提高其光合速率,从而缓解Ca( NO3)2胁迫对番茄幼苗的伤害.     

外源亚精胺对Ca(NO3)2胁迫下番茄幼苗光合特性和抗氧化酶活性的影响

以耐盐性较弱的番茄品种上海‘合作903’幼苗为试验材料,采用营养液栽培方法,研究了叶面喷施1mmol.L-1亚精胺(Spd)对75mmol.L-1 Ca(NO32)胁迫下番茄幼苗生长、叶绿素含量、光合及荧光参数、叶片抗氧化酶活性的影响,以探讨外源亚精胺缓解Ca(NO3)2胁迫伤害的机制。结果显示:Ca(NO3)2胁迫能够显著抑制番茄幼苗的生长;与Ca(NO32)胁迫处理相比,叶面喷施外源Spd 9d后,受胁迫番茄幼苗的株高、茎粗、干重、鲜重分别显著增加70.9%、15.8%、43.4%、41.4%;叶绿素a、b的含量分别提高17.7%、13.8%;净光合速率(Pn)、气孔导度(Gs)、蒸腾速率(Tr)、光合电子传递效率(rETR)和光化学猝灭系数(qP)分别升高6.6%、18.0%、31.0%、4.9%、5.0%,而胞间二氧化碳浓度(Ci)、非光化学猝灭系数(qN)分别降低21.5%、8.1%;超氧化物歧化酶(SOD)、过氧化氢酶(CAT)活性分别增加10.7%和37.5%,而丙二醛(MDA)含量和超氧阴离子(O2.-)产生速率分别显著下降34.5%、17.1%。研究表明,外源Spd通过提高番茄幼苗抗氧化酶活性来有效清除体内活性氧,维持光合机构的稳定性,提高其光合速率,从而缓解Ca(NO3)2胁迫对番茄幼苗的伤害。     

外源H_2S对NO_3~-胁迫下番茄幼苗生理生化特性的影响

采用营养液水培方法,通过外源施加H2S供体NaHS(100μmol/L),研究了信号分子H2S对100mmol/L NO3-胁迫下番茄幼苗生理生化特性的影响。结果表明:(1)NO3-胁迫下,随着处理时间的延长,番茄幼苗的株高、根长、鲜重和干重显著降低,叶绿素(a、b)含量、净光合速率、气孔导度、蒸腾速率均显著降低,而胞间CO2浓度以及丙二醛(MDA)、H2O2含量增加,超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)和抗坏血酸过氧化物酶(APX)活性显著降低,抗坏血酸(AsA)和还原性谷胱甘肽(GSH)含量显著降低。(2)与NO3-胁迫处理相比,外源NaHS处理1、3、5d后,番茄幼苗的株高、根长、鲜重和干重显著增加,叶绿素(a、b)含量、净光合速率、气孔导度、蒸腾速率均显著升高,而胞间CO2浓度显著降低;MDA和H2O2含量降低,SOD、POD、CAT和APX活性显著增强,AsA和GSH含量显著增加,而且幼苗的硝酸还原酶、谷氨酰胺合成酶、谷氨酸合酶的活性显著增强;L-半胱氨酸脱巯基酶活性和内源H2S含量增加。研究认为,外源H2S可能通过提高抗氧化物酶的活性和增加抗氧化物质含量来缓解NO3-对番茄幼苗造成的伤害,从而增强其对NO3-胁迫耐性。     

外源24-表油菜素内酯对弱光胁迫下番茄幼苗生长及光合作用的影响

以弱光敏感型番茄品种‘基尔斯’为试验材料,采用营养液栽培方式,研究了外源24-表油菜素内酯(24-epi-brassinolide,EBR)对弱光(80μmol.m-2.s-1)胁迫下番茄幼苗生长、气体交换参数、叶绿素荧光参数、叶绿素含量、抗氧化酶活性和MDA含量的影响。结果显示,弱光胁迫显著影响番茄幼苗的生长和相关生理指标。而弱光下叶面喷施EBR 15d后,番茄幼苗的茎粗、地上部鲜重、干重、壮苗指数分别显著升高15.8%、29.3%、79.0%、114.5%,净光合速率(Pn)、气孔导度(Gs)、蒸腾速率(Tr)分别显著升高34.1%、46.3%、35.9%,叶绿素荧光参数Fv/Fm、ФPSⅡ、ETR分别升高21.0%、15.4%、16.7%,SOD、POD、CAT和APX活性分别升高16.7%、31.8%、32.7%、51.2%,株高、叶面积、胞间CO2浓度(Ci)、叶绿素总量、MDA含量分别下降9.8%、13.9%、0.9%、13.2%、19.5%。研究表明,适量外源EBR可以通过增强保护酶系统的活性来减轻弱光胁迫造成的膜脂过氧化伤害,有效解除弱光胁迫下番茄幼苗光合作用减弱的非气孔限制因素,维持光合活性,促进幼苗生长。     

干旱胁迫下喷施黄腐酸对燕麦光合及其抗氧化酶活性的影响

为了揭示黄腐酸对干旱胁迫下燕麦光合及其抗氧化酶活性的影响机理,该研究选用燕麦品种‘燕科2号’为材料,采用盆栽试验,以正常供水(田间持水量的75%)为对照(CK),设干旱胁迫处理(田间持水量的45%,D0)、D0 + 喷施不同浓度黄腐酸(0、200、400、600、800、1 000 mg/L)处理(D1~D5),测定各处理燕麦干鲜重、光合性能及其抗氧化酶活性。结果表明:(1)与CK相比,干旱胁迫下燕麦幼苗地上部鲜重和干重、叶片光合色素含量、净光合速率(P_n)、蒸腾速率(T_r)、气孔导度(G_s)均显著降低,并导致叶片F_v/F_m、qP、ETR和Φ_PSⅡ显著下降,使叶片抗氧化酶 SOD、POD、CAT活性分别显著提高25.68%、19.98%和7.29%。(2)与D0相比,D0 +喷施600 mg/L黄腐酸后,燕麦幼苗地上部鲜重和干重分别显著提高了28.59%和39.13%,叶片叶绿素a、叶绿素a+b、类胡萝卜素和P_n、G_s、T_r及F_v/F_m、Φ_PSⅡ、ETR分别显著增加了25.17%、21.03%、47.37%和74.38%、26.47%、43.34%及6.49%、69.57%、70.71%,C_i和F_o、NPQ分别显著降低了19.52%和13.32%、43.75%。(3)干旱胁迫下喷施不同浓度的黄腐酸均使幼苗叶片中SOD、POD、CAT活性较D0处理显著增加,其中喷施600 mg/L黄腐酸的叶片SOD、POD、CAT活性最高,分别较D0处理显著增加了12.19%、76.57%和55.26%。研究认为,叶面喷施适宜浓度黄腐酸能够显著提高干旱胁迫下燕麦幼苗的光合作用及其抗氧化能力,缓解干旱对燕麦幼苗的伤害,进而促进燕麦幼苗的生长,且以叶面喷施600 mg/L黄腐酸效果最佳。     

喷施多效唑提高麻疯树幼苗耐盐性的生理机制

研究了600 mg?L-1 PP333喷施对200 mmol?L-1 NaCl胁迫处理下麻疯树幼苗干重、含水量、叶片细胞超微结构、光合作用、叶片渗透调节能力、叶片丙二醛含量和叶片抗氧化能力的影响。结果表明：600 mg?L-1 PP333喷施处理能显著提高200 mmol?L-1 NaCl胁迫下植株的干重、根冠比和叶片含水量,同时显著降低叶片电解质外渗率（ELP）,降低叶片细胞超微结构的伤害程度,显著提高了其叶绿素含量、净光合速率、渗透调节能力、SOD酶活性和CAT酶活性,显著降低了MDA含量和POD酶活性。可见,PP333喷施能显著提高麻疯树幼苗对盐渍的适应,主要因为其提高了植株的抗氧化能力、光合作用、渗透调节能力。     

外源GSH对盐胁迫下番茄幼苗生长及抗逆生理指标的影响

采用营养液栽培法,研究外源谷胱甘肽(GSH)对NaCl胁迫下番茄幼苗生长、根系活力、电解质渗透率和丙二醛(MDA)、脯氨酸(Pro)、可溶性糖含量以及超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)活性的影响,为利用外源物质减轻盐胁迫伤害提供理论依据。结果显示:(1)NaCl胁迫显著抑制了番茄幼苗的生长、根系活力和SOD、POD、CAT活性,提高了电解质渗透率及MDA、Pro、可溶性糖含量;(2)外源喷施GSH能够诱导NaCl胁迫下番茄幼苗叶片抗氧化酶SOD、POD、CAT活性上调,电解质渗透率及MDA含量下降,Pro和可溶性糖含量恢复至对照水平;(3)外源喷施还原型谷胱甘肽抑制剂(BSO)使NaCl胁迫下番茄幼苗的根系活力以及抗氧化酶SOD、POD、CAT活性下降,脯氨酸含量提高;(4)喷施GSH可诱导BSO和NaCl共处理番茄植株的根系活力、SOD、POD、CAT活性提高,MDA和Pro含量降低。研究表明,外源GSH可通过提高促进盐胁迫下番茄幼苗植株渗透调节能力及清除活性氧的酶促系统的防御能力、降低细胞膜脂过氧化程度、保护膜结构的完整性,从而有效缓解NaCl胁迫对番茄幼苗生长的抑制,提高其耐盐性。     

氯化胆碱对盐胁迫黄瓜幼苗渗透调节物质及活性氧代谢系统的影响

以盐敏感型黄瓜品种津春4号为材料,采用水培方法研究了叶面喷施不同浓度(0.5、1.0和1.5 mmol·L-1)氯化胆碱(CC)对NaCl胁迫(75 mmol·L-1)下黄瓜幼苗鲜重、叶片叶绿素、渗透调节物质含量及活性氧代谢系统的影响.结果表明:(1)单独CC处理可提高黄瓜叶片的叶绿素、可溶性糖和可溶性蛋白含量以及过氧化氢酶(CAT)与过氧化物酶(POD)活性,降低O2·-产生速率,但对植株鲜重及超氧化物岐化酶(SOD)活性影响不大;(2)NaCl胁迫处理增加了黄瓜幼苗叶片中可溶性糖和可溶性蛋白含量,增强了SOD、POD和CAT活性,提高了O2·-产生速率及丙二醛(MDA)的含量,但同时降低了叶绿素含量与植株鲜重;(3)盐胁迫前CC预处理可缓解黄瓜幼苗叶绿素含量和植株鲜重的下降、以及MDA含量和O2·-产生速率的上升趋势,且进一步提高了盐胁迫下黄瓜叶片中SOD、POD和CAT活性.因此,适宜浓度的氯化胆碱可显著提高盐胁迫下黄瓜叶片的抗氧化酶活性,提高清除活性氧的能力,缓解盐胁迫对黄瓜幼苗细胞膜的伤害,增强黄瓜幼苗的耐盐性.     

外源褪黑素对低温胁迫下茄子幼苗生长及其光合作用和抗氧化系统的影响

以‘沪茄08-1’茄子幼苗为试验材料,采用基质栽培方式,研究了叶面喷施50~200μmol·L-1外源褪黑素(melatonin,MT)对低温胁迫[(10±1)℃(昼)/(5±1)℃(夜)]下茄子幼苗生长、光合作用和抗氧化系统等生理指标的影响,以明确外源MT在茄子幼苗抵御低温逆境方面的生理机制。结果显示:(1)低温胁迫处理后,茄子幼苗株高、茎粗、地上部鲜重和根系鲜重、叶绿素含量、叶片净光合速率(Pn)、气孔导度(Gs)和蒸腾速率(Tr)均显著降低,丙二醛(MDA)含量、超氧阴离子产生速率(O-·2)和过氧化氢(H2O2)含量均显著增加。(2)幼苗叶片超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)、谷胱甘肽还原酶(GR)、脱氢抗坏血酸还原酶(DHAR)活性及抗坏血酸(AsA)和谷胱甘肽(GSH)含量均显著升高,而其脯氨酸(Pro)和可溶性蛋白质含量均显著增加;外源MT处理可有效增强低温胁迫条件下茄子幼苗叶片中SOD、POD、CAT、APX、GR、DHAR活性,提高AsA和GSH含量,增加Pro和可溶性蛋白含量,显著抑制其叶片MDA、O-·2及H2O2的积累。研究表明,外源MT主要通过增强低温胁迫下茄子幼苗的光合作用以及清除活性氧的能力,减缓低温胁迫的危害,提高茄子幼苗对低温胁迫的耐性。     

The sodium cycle: A novel type of bacterial energetics

The progress of bioenergetic studies on the role of Na⁺ in bacteria is reviewed. Experiments performed over the past decade on several bacterial species of quite different taxonomic positions show that Na⁺ can, under certain conditions, substitute for H⁺ as the coupling ion. Various primary Na⁺ pumps ( generators) are described, i.e., Na⁺-motive decarboxylases, NADH-quinone reductase, terminal oxidase, and ATPase. The formed is shown to be consumed by Na⁺ driven ATP-synthase, Na⁺ flagellar motor, numerous Na⁺, solute symporters, and the methanogenesis-linked reverse electron transfer system. InVibrio alginolyticus, it was found that , generated by NADH-quinone reductase, can be utilized to support all three types of membrane-linked work, i.e., chemical (ATP synthesis), osmotic (Na⁺, solute symports), and mechanical (rotation of the flagellum). InPropionigenum modestum, circulation of Na⁺ proved to be the only mechanism of energy coupling. In other species studied, the Na⁺ cycle seems to coexist with the H⁺ cycle. For instance, inV. alginolyticus the initial and terminal steps of the respiratory chain are Na⁺ - and H⁺-motive, respectively, whereas ATP hydrolysis is competent in the uphill transfer of Na⁺ as well as of H⁺. In the alkalo- and halotolerantBacillus FTU, there are H⁺ - and Na⁺-motive terminal oxidases. Sometimes, the Na⁺-translocating enzyme strongly differs from its H⁺-translocating homolog. So, the Na⁺-motive and H⁺-motive NADH-quinone reductases are composed of different subunits and prosthetic groups. The H⁺-motive and Na⁺-motive terminal oxidases differ in that the former is ofaa ₃-type and sensitive to micromolar cyanide whereas the latter is of another type and sensitive to millimolar cyanide. At the same time, both Na⁺ and H⁺ can be translocated by one and the sameP. modestum ATPase which is of the F₀F₁-type and sensitive to DCCD. The sodium cycle, i.e., a system composed of primary generator(s) and consumer(s), is already described in many species of marine aerobic and anaerobic eubacteria and archaebacteria belonging to the following genera:Vibrio, Bacillus, Alcaligenes, Alteromonas, Salmonella, Klebsiella, Propionigenum, Clostridium, Veilonella, Acidaminococcus, Streptococcus, Peptococcus, Exiguobacterium, Fusobacterium, Methanobacterium, Methanococcus, Methanosarcin, etc. Thus, the sodium world seems to occupy a rather extensive area in the biosphere.     

Role of the furosemide-sensitive Na+/K+ transport system in determining the steady-state Na+ and K+ content and volume of human erythrocytesin vitro andin vivo

Summary To study the physiological role of the bidirectionally operating, furosemide-sensitive Na⁺/K⁺ transport system of human erythrocytes, the effect of furosemide on red cell cation and hemoglobin content was determined in cells incubated for 24 hr with ouabain in 145mm NaCl media containing 0 to 10mm K⁺ or Rb⁺. In pure Na⁺ media, furosemide accelerated cell Na⁺ gain and retarded cellular K⁺ loss. External K⁺ (5mm) had an effect similar to furosemide and markedly reduced the action of the drug on cellular cation content. External Rb⁺ accelerated the Na⁺ gain like K⁺, but did not affect the K⁺ retention induced by furosemide. The data are interpreted to indicate that the furosemide-sensitive Na⁺/K⁺ transport system of human erythrocytes mediates an equimolar extrusion of Na⁺ and K⁺ in Na⁺ media (Na⁺/K⁺ cotransport), a 1:1 K⁺/K⁺ (K⁺/Rb⁺) and Na⁺/Na⁺ exchange progressively appearing upon increasing external K⁺ (Rb⁺) concentrations to 5mm. The effect of furosemide (or external K⁺/Rb⁺) on cation contents was associated with a prevention of the cell shrinkage seen in pure Na⁺ media, or with a cell swelling, indicating that the furosemide-sensitive Na⁺/K⁺ transport system is involved in the control of cell volume of human erythrocytes. The action of furosemide on cellular volume and cation content tended to disappear at 5mm external K⁺ or Rb⁺. Thein vivo red cell K⁺ content was negatively correlated to the rate of furosemide-sensitive K⁺ (Rb⁺) uptake, and a positive correlation was seen between mean cellular hemoglobin content and furosemide-sensitive transport activity. The transport system possibly functions as a K⁺ and waterextruding mechanism under physiological conditiosin vivo. The red cell Na⁺ content showed no correlation to the activity of the furosemide-sensitive transport system.     

Ouabain resistance of the epithelial cell line (Ma104) is not due to lack of affinity of its pumps for the drug

Na⁺, K⁺-pumps of most eukaryotic animal cells bind ouabain with high affinity, stop pumping, and consequently loose K⁺, detach from each other and from the substrate, and die. Lack of affinity for the drug results in ouabain resistance. In this work, we report that Ma104 cells (epithelial from Rhesus monkey kidney) have a novel form of ouabain-resistance: they bind the drug with high affinity (Km about 4×10^–8 m), they loose their K⁺ and stop proliferating but, in spite of these, up to 100% of the cells remain attached in 1.0 m ouabain, and 53% in 1.0 mm. When 4 days later ouabain is removed from the culture medium, cells regain K⁺ and resume proliferation. Strophanthidin, a drug that attaches less firmly than ouabain, produces a similar phenomenon, but allows a considerably faster recovery. This reversal may be associated to the fact that, while in ouabain-sensitive MDCK cells Na⁺, K⁺-ATPases blocked by the drug are retrieved from the plasma membrane, those in Ma104 cells remain at the cell-cell border, as if they were cell-cell attaching molecules. Cycloheximide (10 g/ml) and chloroquine (10 m) impair this recovery, suggesting that it also depends on the synthesis and insertion of a crucial protein component, that may be different from the pump itself. Therefore ouabain resistance of Ma104 cells is not due to a lack of affinity for the drug, but to a failure of its Na⁺, K⁺-ATPases to detach from the plasma membrane in spite of being blocked by ouabain.We wish to thank Dr. E. Rodríguez-Boulán for the generous supply of Ma104 cells, as well as acknowledge the generous economic support of the National Research Council (CONACYT) of Mexico. Confocal experiments were performed in the Confocal Microscopy Unit of the Physiology Department, CINVESTAV.     

Intracellular calcium content of human erythrocytes: Relation to sodium transport systems

Summary To study the possible role of intracellular Ca (Ca _i ) in controlling the activities of the Na⁺–K⁺ pump, the Na⁺–K⁺ cotransport and the Na⁺/Li⁺ exchange system of human erythrocytes, a method was developed to measure the amount of Ca embodied within the red cell. For complete removal of Ca associated with the outer aspect of the membrane, it proved to be essential to wash the cells in buffers containing less than 20nm Ca. Ca was extracted by HClO₄ in Teflon^® vessels boiled in acid to avoid Ca contaminations and quantitated by flameless atomic absorption. Ca _i of fresh human erythrocytes of apparently healthy donors ranged between 0.9 and 2.8 mol/liter cells. The mean value found in females was significantly higher than in males. The interindividual different Ca contents remained constant over periods of more than one year. Sixty to 90% of Ca _i could be removed by incubation of the cells with A23187 and EGTA. The activities of the Na⁺–K⁺ pump, of Na⁺–K⁺ cotransport and Na⁺/Li⁺ exchange and the mean cellular hemoglobin content fell with rising Ca _i ; the red cell Na⁺ and K⁺ contents rose with Ca _i . Ca depletion by A23187 plus EGTA as well as chelation of intracellular Ca²⁺ by quin-2 did not significantly enhance the transport rates. It is concluded that the large scatter of the values of Ca _i of normal human erythrocytes reported in the literature mainly results from a widely differing removal of Ca associated with the outer aspect of the membrane.     

Metabolism of NAD+ in Nuclei of Saccharomyces cerevisiae during Stimulation of Its Biosynthesis by Nicotinamide

The activities of nuclear enzymes involved in NAD⁺ metabolism in Saccharomyces cerevisiae strain 913a-1 and its mutant 110 previously selected as an NAD⁺ producer were investigated. The presence of extracellular nicotinamide increased the total NAD⁺ pool in the cells and increased [³H]nicotinic acid incorporation; however, NAD⁺ concentration in isolated nuclei decreased slightly. The stimulating effect of nicotinamide on intracellular synthesis of NAD⁺ correlated with increases in ADP-ribosyl transferase, NAD⁺-pyrophosphorylase, and NAD⁺ ase activities.     

Effect of tissue specificity of brain soluble fractions on Na+, K+-ATPase activity

Previous evidence from this laboratory indicated that catecholamines and brain endogenous factors modulate Na⁺, K⁺-ATPase activity of the synaptosomal membranes. The filtration of a brain total soluble fraction through Sephadex G-50 permitted the separation of two fractions-peaks I and II-which stimulated and inhibited Na⁺, K⁺-ATPase, respectively (Rodríguez de Lores Arnaiz and Antonelli de Gomez de Lima, Neurochem. Res.11, 1986, 933). In order to study tissue specificity a rat kidney total soluble was fractionated in Sephadex G-50 and kidney peak I and II fractions were separated; as control, a total soluble fraction prepared from rat cerebral cortex was also processed. The UV absorbance profile of the kidney total soluble showed two zones and was similar to the profile of the brain total soluble. Synaptosomal membranes Na⁺, K⁺- and Mg²⁺-ATPases were stimulated 60–100% in the presence of kidney and cerebral cortex peak I; Na⁺, K⁺-ATPase was inhibited 35–65% by kidney peak II and 60–80% by brain peak II. Mg²⁺-ATPase activity was not modified by peak II fractions. ATPases activity of a kidney crude microsomal fraction was not modified by kidney peak I or brain peak II, and was slightly increased by kidney peak II or brain peak I. Kidney purified Na⁺, K⁺-ATPase was increased 16–20% by brain peak I and II fractions. These findings indicate that modulatory factors of ATPase activity are not exclusive to the brain. On the contrary, there might be tissue specificity with respect to the enzyme source.     

Effects of Tetraethylammoniumchloride (TEA), Vanadate,and Alkali Ions on the Lateral Leaflet Movement Rhythm of Desmodium motorium (Houtt.) Merr

The period (～3-5 min) of the ultradian rhythm of the lateral leaflet movement of Desmodium motorium is strongly lengthened (≤30-40%) by the K⁺ channel blocker tetraethylammoniumchloride (20, 30, and 40 mM) and vanadate (0.5 and 1 mM), which is an effective inhibitor of the plasma membrane-bound H⁺ pump. The alkali ions K⁺, Na⁺, Rb⁺, and Cs⁺ (10-40 mM) shorten the period only slightly (≤ 10–15%). Li⁺ (5-30 mM), however, increases the period of the leaflet rhythm drastically (≤80%). We concluded that the plasmalemma-H⁺-ATP-ase-driven K⁺ transport through K⁺ channels is an essential component of the ultradian oscillator of Desmodium, as has been proposed for the circadian oscillator.