Effects of tetcyclacis on growth and on sterol and sapogenin content in fenugreek

Tetcyclacis, a norbornanodiazetine plant growth retardant, used at 10 mg · L^–1 (36 m), caused greater growth inhibition in the shoots of fenugreek (Trigonella foenum-graecum L.) seedlings (60%) than in the roots (30%), compared with control. This greater retardation was reversed by a supplement of gibberellin (200 mg · L^–1). The total sterol composition of control and treated seedlings was analyzed and quantified. In the roots especially, treatment of seedlings with tetcyclacis resulted in a modification of the sterol profile, leading to an accumulation of 14-methyl sterols, presumably as a consequence of the inhibition of cytochrome P-450-dependent obtusifoliol 14-demethylase. In addition, tetcyclacis caused a significant increase in the cholesterol content of the roots: 38.1% of total sterols against 3.7% in the control roots. However, tetcyclacis was shown to be an ineffective inhibitor of the S-adenosyl-l-methionine (Adomet): cycloartenol-C24-methyltransferase (EC 2.1.1.41) in fenugreek microsomes indicating that cholesterol accumulation does not result from the inhibition of the sterol side chain-alkylating enzyme. Moreover, this accumulation was shown to be concomitant with a significant decrease of the sapogenin content in the treated roots. This last result is discussed with respect to the current proposed pathway by which cholesterol is metabolized to saponins.Abbreviations GA gibberellin - PGR plant growth regulator - GA₃ gibberellin acid - FW fresh weight(s) - DW dry weight(s) - Adomet-CMT S-adenosylmethionine-cycloartenol-C24-methyltransferase - GC gas chromatography - TLC thin layer chromatography - MS mass spectroscopy - FS free sterol(s) - SE steryl ester(s) - SG steryl glycoside(s) - ASG acylated steryl glycosides - SAM S-adenosylmethionine     

Effect of heat stress on development in vitro and in vivo and on synthesis of heat shock proteins in porcine embryos

The present study was conducted (1) to examine the effect of an acute increase in ambient temperature on the development of porcine day 6 embryos in culture and after transfer to recipient gilts, and (2) to analyze intracellular production of heat shock proteins (hsps). The viability of porcine day 6 embryos following a temporary acute elevation in ambient temperature (at 42°–45.5°C and for 10–180 min) was examined. Synthesis of 70 kDa hsp (hsp 70) and 90 kDa hsp (hsp90) was determined by SDS-PAGE and Western blot analysis in porcine day 6 embryos subjected to heat stresses. Nonheat-stressed embryos were considered as control. Significantly higher numbers of viable nuclei were observed in treatment groups of 42°C-10 min (236.6 ± 71.4; P < 0.05) and 43°C-30 min (276.8 ± 89.4; P < 0.005) compared to control (173.9 ± 53.9). The 42°C-180 min group (158.0 ± 27.1 μm) had a greater increase in diameter after 24 hr in culture following heat stress compared to control (82.5 ± 47.3 μm), while heat stress with 43°C for ≧60 min, 44°–44.5°C for ≧30 min, or 45°-45.5°C for ≧10 min impaired their survival, as assessed by differences in number of viable nuclei. The embryos subjected to heat stresses under the conditions of 42°C-180 min, 43°C-10 min, 43°C-30 min, 44°C-10 min, or 45°C-10 min developed to normal piglets after transfer to recipient gilts. Overall pregnancy rate was 75% (6/8), and farrowing rate 62.5% (5/8). Of heat-stressed embryos transferred, 59% (36/61) developed to normal piglets. Heat-stress conditions of 42°C for 180 min, 43°C for 30 min, 44°C for 10 min, and 45°C for 10 min were determined as critical with respect to the in vitro and in vivo survival of porcine embryos. Porcine day 6 embryos constitutively synthesized hsp70 even without heat stress, while hsp90 was detected only at trace level. Neither hsp70 nor hsp90 levels increased in the embryos subjected to heat stresses. In conclusion, porcine day 6 embryos could continue to develop in vivo or during in vitro culture after exposure to acute and temporary rise in temperature. However, no increase of hsp70 and hsp90 was observed in the heat-stressed porcine embryos, while hsp70 was detected in the nonheat-stressed porcine embryos. The precise mechanism of the thermotolerance was unclear. © 1996 Wiley-Liss, Inc.     

Studies on the effects of insulin and acetylcholine on activation of glycogen synthase and on glycogenesis in hepatocytes

The addition of insulin (4.0 × 10^?11 M) or acetylcholine (10^?6 M) to isolated hepatocytes stimulated glycogen accumulation and this stimulation was more pronounced when the medium glucose was raised from 50 to 300 mg percent. Studies with [¹⁴C]-glucose showed a two-fold stimulation in glycogen synthesis by the addition of insulin (4.0 × 10^?11 M) or acetylcholine (10^?6 M). A sixteen percent increase in the activity of glycogen synthase was observed in cells incubated for 10 minutes with insulin (4.0 × 10^?11 M) or acetylcholine (10^?6 M), whereas at one hour incubation a 40 percent increase in activity was observed with the same concentration of insulin or acetylcholine. The effects of insulin and acetylcholine were not additive.     

The growth of Pseudomonas putida on m-toluic acid and on toluene in batch and in chemostat cultures

Summary The present study describes the growth of Pseudomonas putida cells (ATCC 33015) in batch and continuous cultures on two toxic substrates; toluene and m-toluic acid as sole carbon and energy sources. In fed-batch cultures on m-toluic acid up to 3.55 g cell dry weight/1 were achieved with a maximal specific growth rate (_max) of 0.1 h^-1. The average cellular yield was 1.42 g cell dry weight/g m-toluic acid utilized. When liquid toluene was added to shake-flask cultures in the presence of 0.7 g/1 m-toluic acid, the average cellular yield obtained was 1.3 g cell dry weight/g toluene utilized and the _max was 0.13 h^-1. Growth on toluene vapour in the presence of 0.7 g/l m-toluic acid in batch cultures resulted in a cellular yield of 1.28 g cell dry weight/g toluene utilized, with growth kinetics almost identical to those with liquid toluene (_max liquid=0.13 h^-1, _max vapour=0.12 h^-1). The maximal biomass concentration was 3.8 g cell dry weight/l, obtained in both cases after 100 h of incubation. Pseudomonas putida was grown in a chemostat initially on 0.7 g/l m-toluic acid and vapour toluene and then in the steady state on toluene as the sole source of carbon and energy. Toluene was added continuously to the culture as vapour with the inflowing airstream. Chemostat cultures could be maintained at steady state for several months on toluene. The maximal biomass concentration obtained in the chemostat culture was 3.2 g cell dry weight/l. The maximum specific growth rate was 0.13 h^-1, with a cellular yield of 1.05 g cell dry weight/g toluene utilized. Approximately 70% of the toluene consumed was converted into biomass, and the remainder was converted to CO₂ and unidentified byproducts.     

Effect of dietary fibers on glycemia and insulinemia and on gastrointestinal function in rats

The effects of purified and semipurified dietary fiber supplements on glycemia and insulinemia were measured simultaneously with their effects on digestive tract function in the rat. An insoluble fiber (cellulose) and four soluble fibers (guar gum, carboxymethylcellulose, mustard mucilage, and oat beta-glucan) were added separately to a fiber-free solid diet and fed to Sprague-Dawley rats for 10 days. Guar gum and oat beta-glucan reduced the food intake, whereas cellulose increased it. Guar gum reduced weight gain. Cellulose increased the protein efficiency ratio. After a 13-h fast, glycemia and insulinemia were measured 45, 90, 210, and 360 min after the beginning of a voluntary short meal. Addition of fibers did not change the glycemic response, but soluble fibers significantly decreased insulinemia 45 min after the meal. All fibers significantly delayed gastric emptying, cellulose and mustard mucilage being the most effective. Dry matter contents of the small intestine were increased especially by guar gum and oat beta-glucan. All fibers seemed to slow down small intestinal transit and decreased intestinal absorption. In the present experimental situation, both gastric and intestinal components played a role in the hypoinsulinic effect of dietary fibers. The intestinal component appeared to be more determinant for all soluble fibers, except mustard mucilage where the gastric component was more important.     

中国野生植物保护管理的政策、法律制度分析和建议

中国是全球生物多样性最丰富的国家之一。最近40年, 中国的植物多样性保护取得了巨大成就, 实施了多项政策和法律, 尤其是《野生植物保护条例》和《国家重点保护野生植物名录》先后颁布, 奠定了中国植物保护的法律和政策框架, 就地保护和迁地保护网络基本形成。但与生态文明建设的要求相比, 野生植物保护依然存在许多不足。本文系统回顾了中国野生植物保护管理的政策和法律制度, 从就地保护、迁地保护、开发利用活动管理三方面分析了其优缺点并提出建议; 重点对修订《野生植物保护条例》进行讨论并提出建议, 包括修订野生植物和人工培植的定义、优化对开发利用活动的管理程序、加强国际法和国内法的衔接、细化优化罚则等。     

Effect of sucrose diet on insulin secretion in vivo and in vitro and on triglyceride storage and mobilisation of the heart of rats

Basal heart triacylglycerol (TG) (mumole triacylglycerol/g of dry weight) (- before "in vitro" Langendorff perfusion -) was significantly higher in animals rendered chronically hypertriglyceridaemic (H) by a 63% sucrose-rich diet than in controls (C, standard diet); 28 +/- 2.6 means + SEM vs. 19.3 +/- 1.2; respectively (p less than 0.01). After 40' perfusion with Krebs-Henseleit buffer + 5.5 mM glucose, 2.5 mM Ca++, TG content fell to 14.2 +/- 0.6 in C and 14.9 +/- 1.9 in H (n.S.). Administration of 1 n mol x min-1 of glucagon (Gn) from min 20 to 40 reduced TG to 9.0 +/- 0.5 in C (p less than 0.05). In contrast no effect of Gn was observed in H (TG at min 40: 16.7 +/- 2.5). Glycogen (Gly) content (mumol/g of dry weight) after Gn perfusion fell from 30 +/- 1.9 to 17 +/- 2.1 (p less than 0.01) in C, while again no effect was recorded in H. "In vivo" plasma glucose fractional coefficient disappearance rate was lower (p less than 0.001) in H: 1.01 x 10(-2) +/- 0.09 x 10(-2) vs 2.61 x 10(-2) +/- 0.14 x 10(-2) in C, in spite of H showing hyperinsulin secretion. Hyperinsulinism was further documented by "in vitro" Iri release studies from incubated pancreas pieces. In the absence of glucose (G) from the incubation medium H produced 541 +/- 19.8 mU/mg weight Tissue/20', while C produced 91.2 +/- 12.7 (p less than 0.001). With 100 mg% G, H released 1058 +/- 259 and C 377 +/- 82.5 (p less than 0.001). It is suggested that hyperinsulin secretion plus insulin resistance may account for the above findings.     

Effect of reproductive status on twinning and on side of ovulation and embryo attachment in mares

Brood-farm records were used to test several hypotheses concerning twinning and inequalities in the side of ovulation and embryo attachment. Ovulation occurred more frequently (P<0.05) from the left ovary (61% versus 39%) in maiden mares, but with equal frequency from either ovary in lactating and barren mares. The embryo attached more often (P<0.05) to the left horn in lactating mares (60%) and to the right horn in barren (59%) and maiden (67%) mares. Double ovulations and twin embryos were diagnosed more frequently (P<0.05) in barren mares (11% and 6%, respectively) than in lactating mares (5% and 1%). Pregnancy rates for double ovulations were affected (P<0.01) by the length of the interval between the two ovulations (0 days, 83%; 2 days, 87%; 4 days, 67%; 6 days, 54%; 8 days or more, 38%). Pregnancy rates were higher (P<0.01) for double ovulations 0 or 2 days apart (84%) than for single ovulations (54%). Twins were diagnosed more frequently (P<0.05) when double ovulations were two or more days apart (9 32 ) than when the ovulations were synchronous (0 19 ). These results support the conclusion that an embryo-reduction mechanism exists in mares for the elimination of excess embryos and indicate that the mechanism loses its effectiveness when the embryos originate from asynchronous ovulations.     

Different calcium sensitivity in osteoclasts on glass and on bone and maintenance of cytoskeletal structures on bone in the presence of high extracellular calcium

The sensitivity of rat osteoclasts to increased extracellular calcium concentrations ([Ca²⁺]_e) was investigated by single cell measurements of free cytosolic calcium concentrations ([Ca²⁺]_i), by changes in microfilament organization of resorbing osteoclasts, and by in vitro bone resorption assays. Osteoclasts cultured on glass and on bone showed clear differences in their responses, as in 44% and 52% of osteoclasts on glass but in only 21% and 25% of osteoclasts on bone [Ca²⁺]_i increased when [Ca²⁺]_e was increased from 2 mM to 6 or 10 mM via perfusion, respectively. Bone resorption was inhibited without changes in the osteoclast numbers only by 10 mM [Ca²⁺]_e in 2 day cultures. Furthermore, there were no changes in the organization of microfilament structures in resorbing osteoclasts after increased [Ca²⁺]_e (up to 20 mM [Ca²⁺]_e, 30 min incubation). These results suggest that the sensitivity of osteoclasts to increased [Ca²⁺]_e is dependent on their activation phase (resting/migrating vs. resorbing) and that resorbing osteoclasts are not sensitive to increased [Ca²⁺]_e or that the sensing system cannot be reached in polarized resorbing osteoclasts. In contrast, increasing [Ca²⁺]_i through the use of calcium ionophores dispersed specific microfilament structures at the sealing zone transiently in a few minutes. This shows that [Ca²⁺]_i is used as a signaling mechanism to inactivate osteoclasts, with a similar end result on microfilament structures at the sealing zone as caused by increased concentration of cAMP and activation of protein kinase C. © 1996 Wiley-Liss, Inc.