Translocation of leaf-fed 32P in pea plants as influenced by foliar and root applications of CCC and Phosfon

In controlled environment growth chambers, the effects of foliar and root applications of 2-chloroethyltrimethylammonium chloride (CCC) and 2,4-dichlorobenzyltributylphosphonium chloride (Phosfon) on the translocation of³²P fed to leaves, were investigated. When applied to leaves or to root, CCC had no effect on the relative amounts of³²P radioactivity retained by the fed leaf 5, 20 and 80 h after feeding. At 20 and 80 h after feeding, Phosfon concentrations of 0.01 and 0.1mg l^?1 reduced retention of the applied³²P. 80 h after³²P feeding, CCC concentration of 1 mg l^?1 applied as a foliar spray or to the root enhanced the downward movement of³²P. Phosfon at low concentrations, particularly at 0.1 mg l^?1, on the other hand, favoured an upward transport of the applied³²P. Foliar applications of CCC and Phosfon at high concentrations had no significant effect on³²P transport to the root and the shoot below the fed leaf, while root applications of CCC and of Phosfon inhibited downward transport. Root applications generally caused greater alterations in³²P distribution patterns than did foliar applications. On the basis of total active ingredient uptake, Phosfon was more effective than CCC in altering translocation patterns.     

Stimulation of Growth of Peppermint (Mentha piperita) by Phosfon, a Growth Retardant

The shoot growth and fresh weight of Mentha piperita grown in soil were stimulated at concentrations of 1.26 × 10^?5M to 7.77 × 10^?4M phosfon (2,4-dichlorobenzyl tributyl phosphonium chloride) while higher concentrations resulted in retardation of growth. Concentrations of 6.30 × 10^?7M to 3.78 × 10^?5M caused retardation of growth in mineral nutrient solution, and even death at the highest concentrations. However, when the M. piperita plants were grown in mineral nutrient solutions at concentrations of phosfon which had been sequentially lowered from 2.52 × 10^?8M to 2.52 × 10^?12M, the shoot growth and fresh weight were stimulated as in the case of plants grown in phosfon treated soil.     

Non-Reversibility of Gibberellin-Induced Inhibition of Regeneration in Begonia Leaves

With applied to the petioles of detached Begonia x cheimantha leaves before planting, Gibberellic acid (GA₃) inhibited the formation of adventitious buds and roots ill an apparently irreversible manner. Bud formation was entirely suppressed by 10^?6M and higher concentrations and a significant inhibition was still present at 10^?9M the lowest concentration tested. Root formation was not affected by GA₃ below 10^?7M and was possible even at 10^?4 M GA₃. Petiole elongation was stimulated by GA₃ with an optimum at 10^?5M. GA₃ also blocked the action of 6-benzyiamino-purine (BAP) and 1-naphthaleneacetic acid (NAA), compounds which are potent stimulators of bud and root formation, respectively. When applied simultaneously with GA₃ they were, at their optimal concentrations, devoid of any effect in counteracting or reversing the gibberellin-induced inhibitions. Abscisic acid and the growth retardants CCC and Phosfon also were unable to restore bud and root formation. In leaves initially treated with water or 10^?5M BAP, endogenous bud and root formation as well as BAP-induced bud formation were entirety suppressed when 10^?5M GA₃ was applied 8 days after the initial treatments. Even when delayed for 14 days GA₃ treatment inhibited BAP-induced bud formation, while treatment after 21 days bad little effect on bud and root formation. Development of pre-existing, visible bud primordia was not inhibited by GA₃. BAP and NAA competitively inhibited the action of GA₃ in petiole extension growth. The results are discussed in relation to results obtained in other plant systems. It is suggested that GA₃ acts by blocking of the organized cell divisions initiating the formation of bud and root primordia.     

The Influence of NAA, BA and Temperature on Shoot and Root Development from Begonia×cheimantha Petiole Segments Grown in vitro

The effect of exogenously supplied NAA and BA on the shoot and root formation in isolated petiole segments of Begonia×cheimantha was determined in vitro on a modified White medium at a constant temperature of 24°C. The best development of normally appearing plants was obtained on media containing 0.01 mg × 1^?1 of NAA and 0.5 to 1.0 mg × 1^?1 of BA. Lower concentrations of BA yielded no shoots, higher concentrations promoted shoot formation, but the shoots were abnormal with malformed leaves. Lower concentrations of NAA resulted in poorer survival rate and no roots, with higher concentrations of NAA many roots developed, but these were thickened and their longitudinal growth inhibited. Temperature proved to be of utmost importance for the induction of shoot formation. Thus significantly fewer shoots were formed at the higher temperature (25°C) than at lower temperatures (15 to 20°C). Temperature immediately after initial transfer was of greatest importance: 25°C, during the first week followed by low temperature, produced very few shoots.     

Uptake and translocation of root-fed32P in response to foliar and root applications of CCC and phosfon inPisum sativum

The uptake and translocation of³²P applied to nutrient solutions, as influenced by (2-chloroethyl) trimethylammonium chloride (CCC) and 2, 4-dichlorobenzyltributylphosphonium chloride (Phosfon), were investigated in growth chambers. Specific effects depended on the “Retardin”, the method of application, and the concentration. Foliar applications of CCC had no significant effect on³²P uptake 5 h after feeding. At 20 and 80h after feeding, CCC at 100 and at 1 000 mg l^?1 decreased P uptake. With root applications of CCC the same concentrations decreased P uptake as early as 5h after feeding, while the 1 mg l^?1 concentration enhanced P uptake by 40% after 20h. Both the foliar and the root applications of Phosfon influenced P uptake 5h after feeding. With foliar applications the low Phosfon concentration of 0.01 mg l^?1 increased P uptake throughout the experimental period of 80h, but the magnitudes of enhancement declined from 109% at 5h to 63% at 80h. Similarly, the enhancement of P uptake due to the 0.1 mg l^?1 foliar treatment declined from 132% at 5h to 80% at 80h. 100 mg l^?1 CCC enhanced P translocation to the shoot in 5h, with magnitudes of 29% (foliar application) and 64% (root application). At 20 and 80h the stimulations were nullified. The highest concentrations (100 mg l^?1 CCC; 10 mg l^?1 Phosfon) enhanced P translocation 80h after feeding. There were thus general enhancements of P uptake at low concentrations and suppressions at high concentrations, but these effects diminished with time, indicating transitory influences.     

Growth and Organogenesis in Tissue Cultures of Allium cepa var. proliferum

Callus isolated from aerial bulbs of Allium cepa var. proliferum was grown in agar and liquid cultures on a synthetic medium containing 5 × 10^?6M 2,4-D. Root formation occurred in the absence of 2,4-D and was highly stimulated by 5 × 10^?6M NAA. Cytokinin was not necessary for growth and organ formation but slightly stimulated the formation of leafy buds. Combinations of NAA or IAA and cytokinin stimulated growth and root formation to a greater extent than anyone of these substances added alone. Pieces of callus in liquid culture developed roots in one week in root-inducing medium, but bud or embryo formation was not observed in liquid cultures.     

Néoformation caulinaire et radiculaire chez les fragments de feuille deBegonia rex Putz.: Action de divers facteurs régulateurs trophiques et d'environnement

The effects of several growth and trophic substances on bud and root neoformation on leaf fragments ofBegonia rex were studied in precisely defined environmental conditions. IAA, depending on the type of treatment, had different effects. In aseptic cultures, a notable stimulation of bud formation was observed at certain concentrations. However, non aseptic treatments of IAA had no visible effects except at very high concentrations.(10^?3 M) where bud formation was totally inhibited and root formation was favored. NAA, at 10^?6 M and 10^?5 M strongly stimulated root formation and inhibited shoot formation. All the cytokinins used stimulated bud formation and inhibited partially or totally root formation. Gibberellic acid inhibited bud and root formation. Glucose and sucrose clearly stimulated bud and root formation and sucrose, when applied simultaneously with other growth substances, modified the effects of these substances alone. The most favorable environmental conditions were at 24°C in a 24 h photoperiod but other temperatures (17 to 27°C) and photoperiods (9 or 16 h) did not prevent neoformation.     

Growth and the content of laurinterol and debromolaurinterol in Laurencia okamurae (Ceramiales, Rhodophyta)

The growth of Laurencia okamurae and the content of laurinterol and debromolaurinterol were influenced by various factors. Temperature influenced growth raere te with a maximum at 25°C, regardless of daylength. Maturity depended on temperature rather than daylength; the plants grew without maturing at 15°C, while the plants matured within two weeks at 25°C. The plants were able to grow at salinities of 14–50‰ with maximum growth at 26‰. The salinities growth rash;50‰te reduced with decreasing concentration of nitrate below 1.2 × 10^-3 M, and of total phosphate below 7.5× 10^-8 M. Bromide concentration had no effect on growth, and the plants grew without bromide. Variation in temperature between 15–25°C and daylength produced no obvious change in laurinterol and debromolaurinterol contents. On the other hand, an increase in salinity led to an increase for both. The plants cultured in a completely artificial medium, modified ASP₁₂NTA, showed a marked drop in their content of these metabolites. An increase in concentrations of nitrate, total phosphate or bromide did not restore the content. This revised version was published online in June 2006 with corrections to the Cover Date.     

Stimulatory role of smoke–water and karrikinolide on the photosynthetic pigment and phenolic contents of micropropagated ‘Williams’ bananas

At low concentrations, smoke–water (SW) and smoke-derived karrikinolide (KAR₁) are compounds with potential cytokinin and auxin-like activity. Their roles on the growth, photosynthetic pigment and phenolic contents of micropropagated ‘Williams’ bananas were investigated in comparison with meta-topolin (mT). Explants were cultured on modified Murashige and Skoog basal media supplemented with either SW (1:125; 1:250; 1:500; 1:1,000; 1:2,000 dilutions) or KAR₁ at four concentrations ranging from 4.8?×?10^?22 to 3.3?×?10^?12?M. After 42?days, growth parameters were measured while the photosynthetic pigments and phenolic contents were quantified using spectrophotometric methods. Chlorophyll a, b and total carotenoid contents were significantly enhanced by KAR₁ (4.8?×?10^?22?M) and SW (1:125 and 1:1,000 dilutions). The pigments in KAR₁-treated plantlets were approximately two-fold to three-fold higher than those in the control and mT-treated plants, respectively. Total phenolic content was highest with KAR₁ at 1.0?×?10^?19?M in the leaves and 7.8?×?10^?17?M in the roots. Furthermore, KAR₁-treated plants at 1.0?×?10^?19?M yielded the highest level of total phenolics (leaves) and proanthocyanidins (roots). At 1:500 dilutions, SW stimulated the highest total flavonoid content in the leaves across all the treatments. Combining mT with either SW (1:500) or KAR₁ (4.8?×?10^?22?M) significantly increased the quantity of secondary metabolites. However, the growth parameters and pigment contents were not improved. Based on the significant role of photosynthetic pigments and phenolic compounds on the defense and survival strategies of plants, current findings will have practical significance for important processes such as acclimatization and survival of micropropagated plants. These results are also demonstrating the potential of SW and KAR₁ as an eliciting agent for secondary metabolite production.     

Effect of 24-epibrassinolide on growth, protein content and antioxidative defense system of Brassica juncea L. subjected to cobalt ion toxicity

Brassica juncea L. plants were subjected to cobalt (Co) ion (0, 5?×?10^?4, 10^?3, 1.5?×?10^?3 and 2?×?10^?3?M) toxicity and were sprayed with different concentrations of 24-epibrassinolide (24-EBL) (0, 10^?10, 10^?8 and 10^?6?M) at 15-day stage after sowing. They were sampled at 30 and 60?days after sowing and analyzed for growth parameters in terms of shoot length and number of leaves. Thereafter, leaves were excised and content of proteins and the activities of antioxidative enzymes (superoxide dismutase (SOD) (EC 1.15.1.1) catalase (CAT) (EC 1.11.1.6), ascorbate peroxidase (APOX) (EC 1.11.1.11), guaiacol peroxidase (POD) (EC 1.11.1.7) glutathione reductase (GR) (EC 1.6.4.2), monodehydroascorbate reductase (MDHAR) (EC 1.1.5.4) and dehydroascorbate reductase (DHAR) (EC 1.8.5.1)) were analyzed. The plants exposed to cobalt ion exhibited a significant decline in growth in terms of shoot length and number of leaves. However, foliar spray treatment with 24-EBL was able to alleviate the stress generated by cobalt ion and significantly improved the above parameters. The activities of antioxidative enzymes (SOD, CAT, POD, GR, APOX, MDHAR and DHAR) and protein content were also regulated considerably in leaves of plants treated with 24-EBL alone, 10^?8?M concentration being the most effective. The activities of antioxidative enzymes also increased in leaves of B. juncea plants by the application of cobalt ion to soil and consequently sprayed with 24-EBL. Similarly, the protein content was also regulated in leaves of B. juncea plants treated with 24-EBL as compared to untreated control plants, thereby revealing stress-protective properties of 24-EBL.     

The Influence of n-Propanol on the Growth and Conidiation of Pestalotia rhododendri

Pestalotia rhododendri was exposed to vapours from 1 ml propanol solution in water and linear growth, formation of aerial hyphae and production of conidia were determined. A special Petri dish technique was used and maximum stimulation of conidial formation was induced by the vapours from a propanol concentration of 3–4 % (v/v) at 25°C. When propanol was added directly to the medium, a concentration of 1.2 × 10^?2M was optimal for growth and sporulation at 30°C. Sporulation stimulated by propanol was observed at temperatures from 20–32°C, with an optimum at 30°C. Certain observations indicated that an exposure to propanol for 24 hours was enough to induce a stimulated spore production. The stimulation was noticed on different media at 25°C, and was more pronounced at 30°C. One exception was observed. Propanol did not promote sporulation when the fungus was grown on maltagar at 30°C. Propanol 3 ° (v/v) in combination with the standard medium containing (NH₄)₂-tartrate as sole nitrogen source, inhibited the linear growth at 15–20°C, was inactive at 22.5° and 25°C, and stimulated growth at 27.5–31°C. The stimulatory effect was maximal at 30°C. Other media were tested at 25° and 30°C. At both temperatures stimulations of linear growth caused by propanol were observed with a medium containing KNO₃ as sole nitrogen source, and inhibitions with maltagar and another medium containing l -asparaginc as sole nitrogen source. The linear growth could be either inhibited or stimulated while the sporulation was stimulated.     

Adventitious Root Formation Induced by Gibberellic Acid and Regulated by the Irradiance to the Stock Plants

Pea plants (Pisum sativum L. cv. Alaska) were grown from seeds for eleven days at different irradiances. Cuttings were then excised and rooted at 16 W × m^?2. Gibberellic acid (GA₃, 10^?11 to 10^?3M) was applied to the cuttings immediately after excision. Cuttings from stock plants grown at the highest level of irradiance (38 W × m^?2) formed the lowest number of roots. An increasing number of roots per cutting was obtained by decreasing the irradiance to the stock plants. In cuttings from stock plants grown at low irradiances, low concentrations of GA₃ (10^?8 and 10^?7M) promoted root formation further. No effect on rooting by these GA₃ concentrations was observed when applied to cuttings originating from stock plants grown at the high irradiances. Root formation in all cuttings was inhibited by GA₃ at concentrations higher than 10^?6M. The degree of inhibition by GA₃ was influenced by the irradiance pretreatment and was increased with an increase in the irradiance during the stock plant growth. Seeds from different years produced cuttings with different response patterns regarding the irradiance and GA₃ effects on rooting.     

Vegetative Growth Responses of Pea Plants to CCC and Phosfon in Relation to Phosphorus Nutrition

The effects of 2-chloroethyltrimethylammonium chloride (CCC)and 2,4-dichlorobenzyl-tributylphosphonium chloride (Phosfon)on the growth of pea plants in sand culture at two rates ofapplied phosphorus (P), were studied in controlled-environmentgrowth chambers. CCC at 1 and 10 mg/1, and to a lesser degreePhosfon at 0.1 mg/1, stimulated growth. CCC at 1000 mg/1 andPhosfon at 100 mg/1 retarded growth, due mainly to shortenedstems. The magnitude of such effects depended on the level ofapplied P. Reductions in plant height by the 1000 mg/1 CCC treatmentwere 13 and 50 per cent respectively at the high (160 mg/1)and low (8 mg/1) rates of applied P. Similar decreases due to100 mg/1 Phosfon were 30 and 57 per cent respectively. At thehigh P rate, both CCC and Phosfon had no significant effecton total uptake of P, or on relative distribution in the leaf,stem, and root. At the low P rate, the root, relative to leafand stem, retained more P, at a CCC concentration of 1000 mg/1.With Phosfon at 100 mg/1 relative leaf P content increased whilethat of the stem and root decreased. Phosfon was more activethan CCC in terms of the concentration required to cause a givenmagnitude of growth effect.     

Presynaptic Control of the Synthesis and Release of Dopamine from Striatal Synaptosomes: A Comparison Between the Effects of 5-Hydroxytryptamine, Acetylcholine, and Glutamate

The effects of 5-HT and glutamate on dopamine synthesis and release by striatal synaptosomes were investigated and compared with the action of acetylcholine, which acts presynaptically on this system. 5-HT inhibited (28%) synthesis of [¹⁴C]dopamine from L-[U-¹⁴C]tyrosine, at 10-⁵M and above. This contrasts with the action of acetylcholine, which stimulated [¹⁴C]-dopamine synthesis by 24% at 10-⁴ M. Tissue levels of GABA were unaffected by either 5-HT or acetylcholine up to concentrations of 10-⁴ M. The inhibitory action of 5-HT (5 × 10^?5 M and 2 × 10^?4 M) on [¹⁹C]dopamine synthesis was completely abolished by methysergide (2 × 10^?6 M). Higher concentrations of methysergide (10^?4 M) or cyproheptadine (10^?5 M) inhibited [¹⁴C]dopamine synthesis by 28% and 25%, respectively, when added alone to synaptosomes. However, only methysergide prevented the further inhibition of synthesis caused by 5-HT. At concentrations of 2 × 10^?5 M and above, 5-HT stimulated [¹⁴C]dopamine release. This releasing action differed from that of acetylcholine, which occurred at lower concentrations (e.g., 10^?6 M). Methysergide (up to 10^?4 M) or cyproheptadine (2 × 10^?4 M) did not reduce the 5-HT (5 × 10^?5 M)-induced release of [¹⁴C]dopamine, but methysergide (10^?4 M) showed a potentiation (49%) of this increased release. The stimulatory effects of 5-HT (2 × 10^?5 M) and K⁺ (56 mM) on [¹⁴C]dopamine release were additive, indicating that two separate mechanisms were involved. However, when both agents were present the stimulatory effect of K⁺ (56 mM) on [¹⁴C]dopamine synthesis was not seen above the inhibitory effect of 5-HT. Glutamate (0.1-5 mM) did not affect [⁴C]dopamine release or its synthesis from L-[U-¹⁴C]tyrosine. It is concluded that 5-HT modulates the synthesis of dopamine in striatal nerve terminals through a presynaptic receptor mechanism, an action antagonised by methysergide. The releasing action of 5-HT apparently occurs through a separate mechanism which is also distinct from that involved in the response to K⁺ depolarisation.     

Further properties of the polyamine oxidase from oat seedlings

After purification, the polyamine oxidase from the leaves of oat seedlings grown in the dark appeared to be homogeneous on electrophoresis. The MW determined by density gradient centrifugation was 119 000. The enzyme would not oxidise diaminodipropylamine and neither diaminodipropylamine nor diaminopropane were inhibitors at concentrations up to 1 mM. With spermidine as substrate, the energy of activation was 19.7 kJ/mol and activity was reduced to 50% on heating for 10 min at 50°. With spermine as substrate, activity was increased up to 3-fold in the presence of M sodium chloride. This stimulation was not observed with spermidine as substrate The enzyme was also stimulated by sodium phosphate and sodium citrate at high concentrations. The pH for optimal stability was 6.5, the same as the pH for maximum activity with both spermidine and spermine as substrates. For spermidine and spermine the K_ms were 8 × 10 ^?6 M and 2 × 10 ^?6 M respectively. Loss of activity on storage of leaves at ? 15° was ca 5 % per week and in extracts the loss was ca 10 % per week.     

Methyl jasmonate inhibits growth and flowering inChenopodium rubrum

C. rubrum plants of different age were treated with methyl jasmonate (JA-Me), in some cases in combination with photoperiodic flower induction. Plants treated with JA-Me (3×10^?4, 3×10^?5 and 5×10^?7M) showed inhibition of growth and flowering. No effect of JA-Me application on ethylene formation was observed.     

Production of gibberellin-like substance in the embryo of barley during germination

Summary Embryos were excised from barley seeds, their homogenates were incubated with ficin, and their content in gibberellin-like substance was assayed by means of -amylase-producing activity, but no gibberellin-like substance could be detected.Embryos free from endosperm which were cultured for five days produced measurable amounts of gibberellin-like substance. This substance was not produced when a carbon source was absent from the medium, or when air was removed after 2 days of aerobic culture. CCC and Phosfon D (at the concentration of 2×10^-4 M and 0.8×10^-4 M, respectively) inhibited the formation of the gibberellin-like substance in cultured embryos without affecting their growth.Mevalonic acid could be used as a carbon source in the culture of the embryos. The formation of the gibberellin-like substance was in this case inhibited by 0.8×10^-4 M Phosfon D, but was not inhibited by 2×10^-3 M CCC.     

Effetti Morfologici,Anatomici Ed Ultrastrutturali Indotti Dai Ritardanti Di Crescita Su Plantule Di Pisum Sativum L. Var. « Gloria Di Quimper » Cultivate in Soluzione Nutritizia

Abstract

The effect of the growth retardants on the structure of Pea seedlings coltured in nutritive solution. – The addition of CCC (2-Chloro-ethyltrimethyl ammonium chloride) and AMO 1618 (4-Hydroxyl-5-isopropyl-2 methyl-phenyl-trimethylammonium chloride. 1-piperidine carboxylate) to Pea seedlings (Pisum sativum L. var. Gloria di Quimper) promotes the usual modifications induced by growth retardants on higher plants. CCC appears less effective than AMO 1618; CCC inhibits growth only at 10²-M. concentration, on the contrary 5×10-⁵M. AMO 1618 inhibits strongly the growth of the seedlings both in the light and in darkness. CCC and AMO 1618 operate similarly as far as the inhibition of expansion growth, the increase of the stem diameter, and the decrease of the apical dominance are concerned. 10-²M. CCC stimulates both the growth of roots and the secondary roots formation, on the contrary 2,5×10-⁴M. AMO 1618 inhibits strongly the growth of the roots. AMO 1618 affects more strongly than CCC the expantion growth of the leaves. Leaves of the AMO 1618 treated plants are greener than the control plants. Plants treated with CCC and AMO 1618 are smaller because these chemicals inhibit the expantion growth of the cells. The increase of the stem diameter induced by CCC and AMO 1618 is due to the stimulation of the mitotic activity of the cambium. AMO and CCC induce a decrease of the size of the vessels and the sieve tubes. In the sieve tubes of the treated plants and slime plugs appear near to the sieve plates many slime bodies. AMO and CCC did not affect the mitotic activity of the apical meristems; in fact the plants grown in the presence of the growth retardants, show a normal primary body. AMO and CCC delay the lignification process. Chloroplasts of this Pisum sativum variety show prolamellary bodies associated to a good lamellar system. Starch granules are always present. Starch was never found in the chloroplasts of the treated plants. The general picture of the effects induced by growth retardants in Pea seedlings show so many modifications that it is very difficult to believe, like some Authors suggest, that all the effects produced by growth retardants are due to the inhibition of gibberellin biosynthesis.     

A Possible Role for Ferrous Complexes in Fungal Disease Suppression: Glume Blotch and Net Blotch of Cereals

Germination of spores of Septoria nodorum and Pyrenophora teres was inhibited and germ-tube growth in germinated spores was reduced b y ferrous ions complexed with a number of cheiating agents. No such inhibition was observed with ferric complexes and none of the chelating agents in the desferri form was toxic to the fungi. The germination mechanism in spores suspended in ferrous-2,3-dihydroxybenzoic acid (Fe¹¹-DHBA) for 24 h could not subsequently be released to any great extent by incubation with ethylenediamjne-di (o-hydroxyphenyl-acetic acid) (EDDHA). Lesion development by the fungi in the presence of ferrous complexes on detached leaves of host plants was almost totally suppressed, but compounds which preferentially chelate ferric ions, used in the desferri form significantly stimulated lesion development by S. nodorum on wheat leaves. Cermination, appressorium formation and lesion development on leaves of host plants were also significantly reduced by Fe¹¹-DHBA when plants were sprayed to run-off up to 5 days prior to inoculation. Disease development and subsequent 1000 grain weight loss were reduced by approximately 50 percent in wheat and barley plants when the flag leaves were treated with Fe¹¹-DHBA (5 × 10^?4 M) prior to inoculation with S. nodorum and P. teres respectively, compared with inoculated, untreated plants.     

Effects of papaverine on basal and on isoproterenol-stimulated renin secretion from rat kidney slices

Papaverine inhibited the basal renin secretion of rat kidney slices incubated in a physiological salt solution at 37°C. Inhibition was concentration-dependent; secretion was 99 ± 0.2 % inhibited by 5 × 10^?4 M papaverine, and 8 × 10^?5 M was the estimated ED₅₀. In contrast, 2 × 10^?4 M IBMx (3-isobutyl-1-methyl-xanthine) increased the rate of secretion from 215 ± 17 to 366 ± 30 ng hr^?1mg^?1/20 min (p < 0.001). Isoprotenol (4 × 10^?7, 8 × 10^?7, and 5 × 10^?6 M) stimulated renin secretion in a concentration-dependent manner; the stimulatory effects were antagonized by papaverine but unaffected by IBMx. Thus, two known inhibitors of phosphodiesterase--IBMx and papaverine--produce sharply contrasting effects on basal and on isoproterenol-stimulated renin secretion from rat kidney slices.