Changes in the phospholipid content in the left heart ventricle of male mice during repeated administration of isoprenaline

1. Male mice were injected 5 mg/kg isoprenaline (IPRO) daily and the heart weight, dry weight and phospholipid content in the left ventricle determined 24 hr after the last injection on days 1, 3, 5 and 10. 2. The phospholipid content sinks during the experiment, but the onset of the change is different in different phospholipids: for diphosphatidylglycerol it is clearly significant after 3 days, for phosphatidylcholine and phosphatidylethanolamine after 5 days and for sphingomyelin after 10 days; the relative amplitude of the change in this latter phospholipid was greatest of all. 3. If IPRO is given for 3 days and physiological saline for next 7 days, the content of some phospholipids (PE, SM and PG) continued to decrease. This suggests an important delayed effect of IPRO action.     

Reproductive timetable for the tropical Vireya rhododendron,R. Macgregoriae

Summary The reproductive development of Rhododendron macgregoriae F.v.M., Section Vireya (Ericaceae) has been followed from 10 days before anthesis to the production of mature germinable seeds about 145 days after anthesis. The species is self-compatible but shows both protandry and physical separation of pollen from the receptive stigma. Pollen is mature and viable from shortly before anthesis until the corolla and attached anthers abscise some 9–12 days after the flowers open. Spontaneous dehiscence, however, occurs mostly in the first few days after opening. The stigma becomes receptive 6–7 days after anthesis, and nectar is produced at this time. Female gametophytes are not mature until about 10 days after anthesis. Fertilization occurs about 6–7 days after pollination, and although the endosperm commences development immediately, development of the embryo proper does not begin until some 40–45 days later. Pollinations made with fresh pollen between 5 and 14 days after anthesis were successful, but those made on dry stigmas in the first 4 days after anthesis, or on senescing pistils 21 days after anthesis, gave little or no seed set. In nature, autogamy is probably uncommon, the majority of pollinations are likely to be geitonogamous, but there is considerable potential for outcrossing.     

Sex differentiation and pubertal development of gonads in the viviparous mosquitofish, Gambusia affinis

The ontogenetic development of gonads from embryo to adult was observed histologically in the viviparous teleost, Gambusia affinis. Primordial germ cells (PGCs) appeared in the subendodermal space of the embryo 14 days before birth, and then transferred to the dorsal mesentery to form paired genital ridges 12 days before birth. The PGCs proliferated in the genital ridge, forming gonadal primordia 10 days before birth. All gonadal primordia differentiated to the ovary containing oocytes 2 days before birth, but then redifferentiated to the ovary and testis just after birth. This indicates that the mosquitofish is a juvenile hermaphroditic species. The characteristics of gonadal sex differentiation just after birth were enlargement of the oocytes in females, and invasion of somatic cells from the hilar region to an inner portion of the gonad in males. The paired ovary fused at the basal area 5 days after birth, then on the ventral and dorsal portions, developing into a single ovary 10 days after birth. During this time a single ovarian cavity was formed on the dorsal portion of the ovary. The paired testes fused only at the basal area and became a single testis having two main lobes 10 days after birth. The oocytes gradually developed and began vitellogenesis 100 days after birth, but did not reach maturation until 110 days after birth. Spermatogenic cells formed cysts at 20 days, began meiosis at 70 days, and matured to form sperm balls 90 days after birth. The male fish sexually matured earlier than the female.     

Muscle regeneration in adiponectin knockout mice showed early activation of anti-inflammatory response with perturbations in myogenesis

Activation, proliferation, and differentiation of satellite cells can be influenced by extracellular factors, such as adiponectin. This adipokine has been proposed as a regulator of in vitro myogenesis, but its action on in vivo regeneration is not still elucidated. We used C57BL/6 (wild-type [WT]) and adiponectin knockout (AdKO) mice injured with barium chloride at periods of 3, 7, and 14 days after injury. The AdKO presented a higher number of centralized nuclei after 7 days, and a reduction in myogenic genes was observed after 3 days. Moreover, these mice presented an increase in anti-inflammatory cytokines after 3 and 7 days, and an increase in the M2 gene marker and proinflammatory cytokines after 7 days. The WT demonstrated an increase in adiponectin messenger RNA after 7 days. These results demonstrate that adiponectin is important in tissue remodeling during regeneration and that its deficiency does not compromise the maturation of muscle fibers, due to an increase in anti-inflammatory response; however, there is a possible impairment in proinflammatory response and an increase in centralized myonuclei.     

Effects of Adrenalectomy and Replacement Therapy of Corticosterone on Cell Proliferation and Neuroblast Differentiation in the Rat Dentate Gyrus

Newly generated neurons in the dentate gyrus differentiate into mature granule cells. In the present study, we observed the effects of adrenalectomy (ADX) and corticosterone replacement therapy (CRT) on cell death, cell proliferation and neuroblast differentiation in the subgranular zone of the hippocampal dentate gyrus (SZDG). For this, the animals received vehicle or CRT after ADX, and were sacrificed 5 or 42 days later. Plasma corticosterone levels were very low in the adrenalectomized groups, whereas CRT after ADX significant increased serum corticosterone levels at 42 days, not 5 days, after ADX. ADX induced some neuronal damage in the dentate gyrus at 5 days post-ADX. CRT did not significantly reduce the neuronal damage at 5 days post-ADX; however, neuronal damage was not shown at 42 post-ADX with CRT. Ki67 (a marker for cell proliferation) and doublecortin (DCX, a marker for neuronal differentiation) immunoreaction was detected in the SZDG. ADX transiently increased cell proliferation and neuroblast differentiation 5 days after ADX, not 42 days, after ADX, and the CRT 42 days after ADX prominently decreased cell proliferation and neuroblast differentiation in the dentate gyrus. These results suggest that adrenal corticosteroid hormone is not essential for cell proliferation and neuroblast differentiation in long-term period after ADX.     

Photoperiodic control of the termination of reproduction in Japanese quail (Coturnix coturnix japonica)

Typically, birds come into breeding in the spring as a response to long days, and end reproduction some weeks later by becoming refractory to those long days. The refractory state is subsequently dissipated by the short days of autumn and winter, so producing once again a bird that can respond to long days. Bird species differ in the extent to which refractoriness is developed; the present experiments took advantage of the relative, rather than the absolute, refractoriness in quail to measure quantitatively the dissipation process. Quail were made refractory by exposure to long days, then transferred to short days and at various times thereafter photostimulated with longer daylengths, the degree of photoresponsiveness being assessed by measuring changes in luteinizing hormone (LH) secretion or cloacal gland size or both. The most clearcut results came from using 13L:11D as the test stimulus to measure photoresponsiveness, and this indicated, in both intact and castrated quail, no response to 13L:11D after one week of short days, a minor response after two weeks, a strong response after three weeks and a full response after five weeks. Thus refractoriness appears to be dissipated gradually under short days, and not in an all-or-none fashion. Confirmation of this conclusion came from experiments in which refractory quail were moved to short days and after one or two weeks transferred to a range of long daylengths. After one week of short days no responses were obtained to 13L:11D or 14L:10D and moderate responses only to 16L:8D, but after two weeks of short days the magnitudes of all the responses were increased.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of aluminum on erythroidal cells in bone marrow in rats

The study has been carried out on Wistar rats. The aim of the present study was to trace the effect of aluminum on erythroidal cells in bone marrow in rats. The number of proerythroblast after 10 days of experiment with aluminum slowly decreased up to 80 days of experiments. However, the number of basophilic erythroblasts after 10 days insignificantly increased but after 20 days gradually decreased up to 80 days of experiments. The bone marrow polichromatic erythroblasts after 10 days of experiment slightly decreased, however after 20, 40 and 80 days of experiments the values decreased significantly. The quality of orthochromatic erythroblasts after 10 days of experiments dropped and after 20, 40 and 80 days of experiments significantly decreased compared to the control value. Aluminum also brings about histological changes in the bone marrow. The statistical significant reductions of hemoglobin and hematocrit levels were found in the aluminum exposed rats.     

Residual toxicity of some insecticides on the predatory bugs Dicyphus tamaninii and Macrolophus caliginosus

Chlorpyrifos, formetanate, methamidophos, imidacloprid and endosulfan were tested in the laboratory for their effects upon the mirid bugs Dicyphus tamaninii and Macrolophus caliginosus, which are polyphagous predators used for IPM programs in some vegetable crops. The mortality of third-fourth instar nymphs was checked 24 and 48 hours and 7 days after exposure to 1-, 3-, 8-, 21- and 30-day residues of the treatments on tomato leaflets. The reproductive capacity of surviving females also was evaluated for 15 days and compared with females that had not been exposed to insecticides. Chlorpyrifos, formetanate and methamidophos are considered persistent because they remained toxic to both mirid species for 30 days. Imidacloprid is moderately persistent, becoming harmless by 21 days after treatment for M. caliginosus and by 30 days after treatment for D. tamaninii. Endosulfan is moderately persistent for M. caliginosus, becoming harmless by 21 days after treatment, and is short lived for D. tamaninii, becoming harmless by 3 days after treatment. There were no effects on the reproductive capacity of females that were exposed as nymphs to the insecticides tested. Of all the insecticides, only endosulfan is marginally compatible with the use of D. tamaninii.     

Ontogeny of the circadian system controlling release of sperm from the insect testis.

In the gypsy moth, the release of sperm bundles from the testis into the vas deferens is rhythmic and is controlled by a circadian pacemaker located in the reproductive system. However, in males kept since pupation in constant darkness (DD) and temperature, the release of sperm was arrhythmic. The release of sperm became rhythmic when males were transferred from a light-dark cycle (LD 16:8) to DD 6-7 days after pupation. To further investigate the development of the circadian system during the pupal stage, we exposed DD pupae to a single 8-hr pulse of light or 8-hr pulse of a 4 degrees C temperature increase on different days after pupation. The pattern of sperm release was determined 5-6 days after the pulse. Males that were exposed to light or temperature pulses 5 days after pupation subsequently showed nonrhythmic sperm release. However, about half of the pupae that received the pulse on day 6 and most of the pupae that received it on day 7 subsequently showed synchronized sperm release. These results suggested that the clock underlying rhythmic release of sperm becomes operational at approximately 6 days after pupation--that is, 2 days prior to initiation of rhythmic sperm release from the testis.     

Hepatic cholesterol synthesis and hydroxymethylglutaryl CoA reductase activity after injection of methylazoxymethanol acetate

Cholesterol synthesis and 3-hydroxy-3-methylglutaryl CoA reductase (HMG-CoA reductase) in the liver of rats at various times (7, 22, 45 and 314 days) after injection with the carcinogen, methylazoxymethanol acetate (MAMA) is reported. Seven days after treatment, an increase in both cholesterol synthesis and HMG-CoA reductase activity was observed. Elevated HMG-CoA reductase activity and reduced dietary feedback was present 22 days after carcinogen. Cholesterol synthesis was normal at this time but dietary cholesterol failed to significantly reduce synthesis. Forty-five days after carcinogen both cholesterol synthesis and HMG-CoA reductase activity had returned to normal. Both parameters were normal 314 days after carcinogen. The enzyme gamma-glutamyl transferase was also elevated at 7, 22 and 314 days. These results indicate that HMG-CoA reductase activity and cholesterol synthesis exhibit different regulatory characteristics during the early stages of hepatocarcinogenesis initiated by MAMA injection.     

Regulation of cell growth by selective COX-2 inhibitors in oral carcinoma cell lines

Evidence indicates that NSAIDs that inhibit prostaglandin (PG) synthesis can reduce the incidence of colorectal cancers and that inhibition of cyclooxygenase-2 (COX-2) may be the underlying mechanism. The objective of this study was to investigate this putative mechanism by examining the effect of selective COX-2 inhibitors (Celebrex, DFU, NS-398) and COX-1 inhibitors (Aspirin) on the growth of two human oral carcinoma cell lines (OEC-M1 and KB) and one normal fibroblast cell line (NF). We found that the growth of OEC-M1 cells could be significantly inhibited by DFU concentrations above 30 microM (31%) after 4 days, and above 50 microM (35%) after 2 days in culture; by Celebrex at concentrations above 20 microM (52%) after 6 days, above 30 microM (36%) after 5 days, and above 40 microM (33%) after 4 days in culture; and by NS-398 above 1 microM (30%) after 6 days, and above 10 microM (35%) after 5 days in culture. The growth of KB cells could be significantly inhibited by DFU concentrations above 10 microM (33%) after 6 days, above 20 microM (35%) after 4 days in culture; and by Celebrex at concentrations above 10 microM (33%) after 5 days, and above 50 microM (30%) after 4 days in culture; and by NS-398 above 1 microM (45%) after 5 days, above 20 microM (36%) after 4 days in culture. The growth of NF cells could be significantly inhibited by DFU above 30 microM (45%) after 6 days, and above 40 microM (32%) after 3 days in culture, and by Celebrex at concentrations above 10 microM (42%) after 6 days, above 30 microM (31%) after 4 days, above 50 microM (32%) after 3 days in culture, and by NS-398 above 0.1 microM (35%) after 4 days, and above 1 microM (32%) after 3 days in culture. The growth-inhibitory concentration (IC50) values for DFU on OEC-M1, KB, and NF cells were about 39.1, 14.8, and 42.9 microM at 144 h, respectively, and on KB was about 45.2 microM at 120 h. The IC50 values for Celebrex on OEC-M1, KB, and NF cells were about 19.1, 8.6, and 15.8 microM at 144 h, respectively, and on KB and NF were about 27.7 and 35.3 microM, respectively, at 120 h. The IC50 values for NS-398 on OEC-M1, KB, and NF were about 18.9, 0.7 and 1 microM, respectively, at 144 h; on KB and NF values were about 10.8 and 1.4 microM, respectively, at 120 h and on KB and NF were about 26.6 and 4.1 microM, respectively, at 96 h. The results show that the growth of these cell lines is inhibited by three COX-2 selective inhibitors but not by any COX-1 selective inhibitors. These findings suggest that COX-2 may play an important role in the generation of biochemical mediators that stimulate the growth of human oral cancer and normal fibroblast cell lines.     

Modulation of Host Gene Expression during Initiation and Early Growth of Nodules in Cowpea, Vigna unguiculata (L.) Walp

Inoculation of 2-day-old cowpea (Vigna unguiculata [L.] Walp.) seedlings with Rhizobium fredii USDA257 results in proficient nodulation of the tap root. The most abundant nodulation occurs in a region roughly corresponding to the position of the root tip at the time of inoculation. We have examined plant gene expression in this region, after inoculation with either USDA257 or a nonnodulating mutant, 257B3. After isolation of mRNA and in vitro translation, the protein products were separated by two-dimensional gel electrophoresis. Seven proteins are induced within 2.5 days after inoculation with USDA257. One additional induced protein is detectable by 3.5 days after inoculation, and three more appear by day 6. Three of the proteins that are differentially expressed at 2.5 and 3.5 days after inoculation are produced at equivalent levels after 6 days, indicating transient induction of these genes during early stages of nodule development. Several proteins were more abundant in translations of mRNA from roots that had been inoculated with the nonnodulating mutant. This was particularly true after 6 days, when nine proteins were in this class. Thus, altered plant gene expression in carefully selected, highly responsive tissue can be detected 2 days before emerging nodules are visible on the roots, and 6 to 7 days before acetylene reduction is detectable. Additionally, comparisons of ionically bound cell wall proteins isolated 6 days after inoculation revealed four that were unique to nodulating roots, suggesting that some of the nodulation-induced genes may code for structural proteins.     

Disaccharidases in the small intestine of the mouse: normal development and influence of cortisone, actinomycin D, and cycloheximide

The development of maltase, sucrase, and lactase activity has been examined in the small intestine of the mouse. After increasing during 2 days before birth, maltase remains unchanged for 14 days, after which activity surges up throughout the intestine. Sucrase is absent during the first 14 days, but then rises in a pattern similar to, but distinct from, that for maltase. Both enzymes rise faster in the proximal third of the intestine than in the terminal third. Lactase, which is high in the infant intestine, falls after 12 days in the proximal segment, but only after 16 days in the more posterior segments.Cortisone administered at 8 days causes a rise of maltase activity that continues for at least 72 hours. At 4 days the same treatment causes an increase that ceases after 48 hours. Sucrase activity is elicited by cortisone at 8 days but not at 4 days. Between 10 and 13 days both actinomycin D and cycloheximide evoke significant increases of both maltase and sucrase activity in all regions of the intestine. When administered in concert with cortisone, actinomycin D inhibits, but does not prevent, the stimulatory influence of the hormone on sucrase; with maltase activity, significant inhibition occurs only in the middle third of the intestine. Cycloheximide does not interfere with the effects of cortisone. No additive effects between hormone and antibiotics were obtained.These results are discussed in relation to results of similar studies on intestinal alkaline phosphatase and leucylnaphthylamidase.     

Single dose exposure of sarin and physostigmine differentially regulates expression of choline acetyltransferase and vesicular acetylcholine transporter in rat brain

Choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT) are the key components of cholinergic system apart from acetylcholinesterase. Effects of subcutaneous exposures of 0.25 and 0.5 LD(50) sarin and 0.75 mg/kg physostigmine on immunoreactivity levels of these two proteins (ChAT and VAChT) were studied. Immunoreactivity levels of ChAT decreased significantly after 1 and 3 days in cortex and 3 days of 0.25 LD(50) sarin administration in cerebellum. While 0.5 LD(50) sarin exposure caused significant down regulation after 2.5 h to 7 days in cortex and 1 and 3 days in cerebellum with respect to controls. Physostigmine at 0.75 mg/kg dose showed enhanced levels of ChAT after 1 day which decreased significantly after 3 and 7 days both in cortex and cerebellum compared to controls. VAChT level decreased significantly after 1 day in cortex and 3 and 7 days in cerebellum after 0.25 LD(50) sarin administration, while 0.5 LD(50) sarin significantly lowered VAChT immunoreactivity level after 2.5 h and 7 days in cortex and 2.5 h and 1 day in cerebellum. Physostigmine at 0.75 mg/kg dose showed significant enhanced immunoreactivity levels of VAChT after 1, 3, and 7 days in cortex and 3 days in cerebellum. Results show that acetylcholinesterase inhibition by sarin caused reduction in cholinergic neurotransmission at cholinergic proteins expression levels, while physostigmine caused differential expression of key cholinergic proteins. Moreover, cortex, which receives greater cholinergic innervations, is more susceptible to anticholinesterase effect on cholinergic gene expression. These changes can explain delayed neurocognitive changes during anticholinesterases induced chronic neurotoxicity.     

Effects of starvation on the parathyroid glands in golden hamsters of different ages, with special reference to the frequency of lipid droplets

The frequency of lipid droplets in the parathyroid glands of young, adult and senile golden hamsters after starvation was investigated. In the parathyroid glands of the young and senile golden hamsters, the number of lipid droplets increased to reach a peak by 2 days, then decreased slowly by 5 days after starvation, and decreased rapidly after refeeding. In the glands of adult animals it increased to reach a peak by 5 days after starvation and decreased rapidly after refeeding. These findings suggest that in the fasting condition there is a relationship between the number of lipid droplets and aging.     

Reversible Inhibition of Acetylcholine Synthesis and Behavioural Effects Caused by 3-Bromopyruvate

3-Bromopyruvate inhibits pyruvate decarboxylase in brain homogenates and causes a 90% drop in acetylcholine tissue content at a concentration of 2 mM. Stereotaxic injection of 3-bromopyruvate into the basal forebrain causes after 7 days a 40% drop of acetylcholine concentration and pyruvate decarboxylase activity in the cortex and hippocampus, and greater decreases at the site of injection. However, values return to normal 18 days after injection. Choline acetyltransferase is partially inhibited only at the site of injection after 7 days. Choline transport and choline concentration are not affected at either 7 or 18 days after injection. Impairments in spontaneous alternation and in retention of passive avoidance were seen only 7 days after the injection. The results suggest that stereotaxic injection of bromopyruvate can induce discrete reversible cholinergic lesions on a time scale useful for behavioural experiments and for comparison with neurodegeneration.     

Monitoring of changes in physical and microbiological properties of a Chernozem amended with different organic substrates

A soil microcosm study was made to monitor changes in soil physical and microbiological properties of a Chernozem during a period of up to 126 or 252 days following the addition of whey, straw or vegetable oil. In the whey treatment soil maximum water-holding capacity (MWHC) had decreased after seven and 28 days of incubation. At both dates, the differences to the untreated control were significant. Straw was able to increase MWHC of soil during incubation and after 42 and 126 days values differed significantly from those of the control. Compared with the control, whey, oil and straw treatments had higher meanweight diameter of dry aggregates. The differences were significant after seven, 28 and 126 days with whey, after 42, 126 and 252 days with oil, and after 126 days with straw. The sensitivity of dry aggregates to abrasion (SAA), representing a negative index of dry aggregate stability, was lower in the whey treatment than in the control after three and seven days incubation. In the later phase of incubation, whey tended to increase SAA. A trend to increase SAA also was observed with straw and after 126 days a significantly higher SAA for the straw than for the oil treatment was determined. This trend still was to observe after 252 days incubation. An increase in SAA observed for the oil treatment after 42 days was followed by a decrease till the end of incubation. Aggregates of organic treatments were more resistant to the dispersive effect of water than those of the control. Microbial biomass-C contents were high in the whey treatment, ranging between 1931 and 754 g g^–1 soil dry mass during incubation. With whey, fungal contributions to biomass-C increased from 40.5% after three to 76.5% after 126 days incubation. Addition of straw or oil stimulated biomass synthesis less than whey. High fungal contributions to biomass-C, approx. 70%, were sustained by straw during incubation. With oil, fungal contributions were 20.5% after three, 76% after 42 and less than 20% after 126 and 252 days incubation. Fungal contributions to biomass-C correlated positively with SAA. High sensitivity of the fungal biomass to mechanical stress is discussed as a cause for the low dry aggregate stability of soils amended with organic substrates encouraging fungal biomass development.     

傅氏凤尾蕨配子体发育及其无配子生殖的研究

采用光学显微镜对傅氏凤尾蕨（Pteris fauriei Hieron.）的配子体发育进行了研究。傅氏凤尾蕨孢子深褐色,呈四面体形,三裂缝,极面观为钝三角形,赤道面观近半圆形。孢子自播种3～7 d左右开始萌发,萌发类型为书带蕨型。18 d左右发育为丝状体,大约为6～10个细胞长;25 d左右,丝状体可通过顶端细胞或中间细胞分裂产生片状体。播种40～50 d左右,在片状体的侧面产生分生组织,发育成原叶体,发育类型为水蕨型。雄配子体形状不规则,其上可产生精子器。大型原叶体形状较规则,顶端为心形,发育2～3个月左右,在生长点下方产生无性胚芽,进行无配子生殖。此后不久,在胚芽和生长点之间产生导管连接孢子体和配子体。经多次培养表明傅氏凤尾蕨不产生颈卵器,为专性无配子生殖。     

Onset of amnesia is delayed with a decrease in inhibition of protein synthesis during odor-taste associative learning in the terrestrial slug Limax valentianus

Slugs can retain odor-taste associative memory for several weeks, and this requires protein synthesis. We examined the dose-dependency of the onset time of amnesia caused by the protein synthesis inhibitor anisomycin, and showed that with reduced dose, the onset is shifted from 2 days to 3 days after conditioning; we could not shift the onset delay later than 3 days. Our results suggest that the mechanism underling memory retention is different in the period up to 3 days, versus the period later than 3 days. Our results also suggest that sustained inhibition of protein synthesis in the period from zero to 3 hr after conditioning is necessary to cause amnesia.