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1.
KAORU NIKI KATSUTOSHI YOSHIZATO HIDEO NAMIKI SAKAÈ KIKUYAMA 《Development, growth & differentiation》1984,26(4):329-338
DERBY successfully maintained the tail of tadpole ( Rana pipiens) in vitro over a period of 2 weeks in a physiological salt solution (1). When we tried to apply DERBY'S methods of the tissue culture to tadpoles of bullfrog, Rana catesbeiana , it was found that the tissue regressed spontanously without stimulation of thyroid hormone. Several different media were examined in order to select a better culture medium for the bullfrog tadpole tissues. RPMI-1640 medium supplemented with insulin and transferrin was found to be satisfactory for this aim. With this improved medium, the interaction between the epidermis and the mesenchyme has been investigated during the hormone-induced tadpole tail regression and the epidermal dependence of the mesenchyme regression was demonstrated by the following three experiments. (i) Some of surgically prepared mesenchymes regressed in responce to thyroid hormone. In these cases the mesenchymes were revealed to be contaminated with the remaining epidermal cells. (ii) Complete removal of the epidermis was accomplished by the chemical treatment. The mesenchyme thus obtained ("nude tail fin") was insensible to thyroid hormone. (iii) "Skin conditioned medium" (SCM) was prepared by culturing the skin in the presence and absence of thyroid hormone. Nude tail fin regressed when cultured in the SCM containing thyroid hormone. 相似文献
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S¸ükrü Beydemİr İlhami Gülçİn 《Journal of enzyme inhibition and medicinal chemistry》2013,28(2):193-197
The in vitro effects of melatonin (N-acetyl-5-methoxytryptamine) on human carbonic anhydrase isozymes (HCA-I and HCA-II) from human erythrocytes and in vivo effects on rat erythrocytes carbonic anhydrase (CA) were determined. Human erythrocyte carbonic anhydrase isozymes were purified by haemolysate preparation and Sepharose-4B-L tyrosine-sulfanilamide affinity gel chromatography. The HCA-I enzyme, having a specific activity of 7337.5?EU/mg protein, was purified 843-fold with a yield of 60% and the HCA-II enzyme, having a specific activity of 17067?EU/mg protein, was purified 1962-fold with a yield of 22.7%. For in vitro experiments, the enzyme activity was minimal at 2×10-4?M melatonin concentration and increased above this concentration. Ten mg?kg-1 melatonin was administered intraperitoneally and showed a stimulatory effect on the enzyme. Time-dependent in vivo studies were conducted for melatonin in Sprague–Dawley type rats. It was found that CA activity in the rat erythrocytes was decreased by the melatonin after 1 and 3 hours to 2500±500.0 and 1875±239.4 respectively which were statistically significant (p<0.05) differences to the control (2660±235.8). However, CA activity was restored to its normal level after 6?h (2666±235.7) (p>0.05) probably due to metabolism of the melatonin. The findings indicate that melatonin may be pharmacologically useful in some diseases. 相似文献
4.
Miguel Arredondo Héctor Núñez Guadalupe López Fernando Pizarro Mariana Ayala Magdalena Araya 《Biological trace element research》2010,134(3):252-264
Classic copper indicators are not sensitive and specific for detecting excess copper exposure when this is higher than customary
but not markedly elevated. Serum copper and ceruloplasmin (Cp) are the most commonly used indicators to assess nutritional
status of copper. The objective of this paper was to study the influence of estrogens on these indicators and others used
to assess early effects of excess copper exposure in humans and the expression of a set of copper related proteins in a hepatic
cellular model. For the studies in humans, 107 healthy participants (18–50 years) were allocated as follows: group 1 (n = 39), women assessed on day 7 of their hormonal cycle; group 2 (n = 34), women assessed on day 21 of their hormonal cycle, and group 3 (n = 34, comparison group), healthy men. Participants received 8 mg Cu/day (as copper sulfate) during 6 months. Serum Cp and
Cu, Cu–Zn–superoxide dismutase activity, liver function indicators [aspartate aminotransferase (AST), alanine aminotransferase
(ALT), and gamma glutamyltransferase (GGT)], and serum Fe and Zn concentrations were measured monthly. In addition, the influence
of estradiol on intracellular total copper content, hctr1, dmt1 and shbg mRNA abundance and hCTR1, and DMT1 expression was
measured in HepG2 cells. Serum Cu, Fe, and Zn and liver aminotransferases but not Cu–Zn–superoxide dismutase varied depending
on sex. Fe nutrition indicators, GGT, and ALT activities showed significant differences between the hormonal phases. Cellular
experiments showed that estradiol increased cellular Cu concentration and hCTR1 and DMT1 mRNA expression and changed these
proteins expression patterns. Estradiols significantly influence the responses to copper at the whole body and the cellular
levels, suggesting that they help maintaining copper availability for metabolic needs. 相似文献
5.
Cationic Liposomes Enhance the Rate of Transduction by a Recombinant Retroviral Vector In Vitro and In Vivo
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Colin D. Porter Katalin V. Lukacs Gary Box Yasuhiro Takeuchi Mary K. L. Collins 《Journal of virology》1998,72(6):4832-4840
Cationic liposomes enhanced the rate of transduction of target cells with retroviral vectors. The greatest effect was seen with the formulation DC-Chol/DOPE, which gave a 20-fold increase in initial transduction rate. This allowed an efficiency of transduction after brief exposure of target cells to virus plus liposome that could be achieved only after extensive exposure to virus alone. Enhancement with DC-Chol/DOPE was optimal when stable virion-liposome complexes were preformed. The transduction rate for complexed virus, as for virus used alone or with the polycation Polybrene, showed first-order dependence on virus concentration. Cationic liposomes, but not Polybrene, were able to mediate envelope-independent transduction, but optimal efficiency required envelope-receptor interaction. When virus complexed with DC-Chol/DOPE was used to transduce human mesothelioma xenografts, transduction was enhanced four- to fivefold compared to that for virus alone. Since the efficacy of gene therapy is dependent on the number of cells modified, which is in turn dependent upon the balance between transduction and biological clearance of the vector, the ability of cationic liposomes to form stable complexes with retroviral vectors and enhance their rate of infection is likely to be important for in vivo application. 相似文献
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William W. Yotis 《Journal of bacteriology》1967,94(5):1353-1358
Norethindrone has been examined in vitro for antibacterial activity against 10 microorganisms. Turbidimetric techniques were used to assay the antibacterial activity of norethindrone. The organisms tested included Staphylococcus aureus, S. epidermidis, Micrococcus conglomeratus, Listeria monocytogenes, Streptococcus faecalis, Salmonella typhosa, Shigella flexnerii, Klebsiella pneumoniae, Escherichia coli, and Proteus vulgaris. Bacteriostatic action was shown only against the gram-positive microorganisms when they were grown anaerobically in Tryptic Soy Broth containing 10 to 50 mug of norethindrone per ml. The bacteriostatic action of norethindrone was exerted primarily during the first 8 hr of incubation and it was reduced by the presence of oxygen. Mestranol at a concentration of 1 to 10 mug/ml failed to exert any significant action on S. aureus. However, incorporation of 5 mug of mestranol per ml in the culture medium enhanced the bacteriostatic action of norethindrone on staphylococci. Enhancement of the bacteriostatic action of norethindrone could not be obtained by the addition of a concentration of 5 mug/ml of testosterone, 17alpha-estradiol, and 17beta-estradiol. Progesterone and 4-pregnen-20beta-ol-3-one under similar conditions showed an additive bacteriostatic effect when they were incorporated into the culture medium containing norethindrone. In vivo studies indicated that female, adult New Zealand rabbits, injected subcutaneously with two injections of 10 to 20 mug of norethindrone, 24 hr apart, and challenged intradermally with S. aureus 4 hr after the second injection, had fewer lesions with smaller areas of swelling and erythema as compared to control, nontreated rabbits. The protective effect of norethindrone on the development of staphylococcal lesion seemed related to hormone concentration. Thus, it was demonstrated with doses of 20, 15, and 10 mug, but not with doses of 1 and 5 mug. When the lesions were excised 48 to 92 hr after infection and when viable cell counts were made, rabbits treated with norethindrone showed significantly lower staphylococcal counts than the control rabbits. During the 1st day after infection with S. aureus, leukocytic counts of the norethindrone-treated rabbits remained normal, whereas control animals showed elevated leukocytic counts. 相似文献
7.
Pyocin, a bacteriocin obtained from lysates of ultraviolet-induced cultures of Pseudomonas aeruginosa was characterized in vitro and in vivo after 1,000-fold purification by chemical, column, and differential centrifugation procedures. Electron micrographs of negatively stained pyocin preparations contained rod-shaped particles which resembled the contractile tail protein of the T-even phages of Escherichia coli. Although two separate and distinct pyocin fractions were eluted from diethylaminoethyl cellulose (pH 7.5) during the purification procedure, the particles appeared identical. In addition, the two fractions exhibited a close correlation between their titers and the particle numbers as observed in the electron microscope. The particles were approximately 20 by 90 mmu with a core diameter of 5 mmu and a sheath length of 50 mmu. Neither intact phage nor ghosts were seen in any of the preparations, although ringlets of two different diameters, which appeared to correspond to the diameters of the sheath and inner core, were observed. Other studies indicated that, although crude preparations were stable to freezing and thawing, purified preparations lost all of their activity under similar treatment. However, the addition of 50% glycerol to purified preparations completely protected activity. Conversely, aged normal human or rabbit sera enhanced the antibacterial activity of pyocin approximately fourfold, although serum albumin and hemoglobin had no effect. In vivo studies indicated that purified pyocin was not lethal for mice when injected intraperitoneally in concentrations of 28,000 to 1,400,000 units (5.6 to 276 mug of protein), nor was 7,200 to 36,000 units dermonecrotic for rabbits. 相似文献
8.
SYNOPSIS. A diversity of issues related to metamorphosis arediscussed in this paper, ranging from biomechanical constraintson behavior in premetamorphic anurans, to environmental factorsthat regulate metamorphosis. I begin by reviewing key behavioralfeatures of tadpoles that have implications to their form andlocomotion. Tadpoles lack all visceral behaviors, such as emesis, coughing,and egg-laying, that require major elevations of pressure inthe pleuroperitoneal cavity. I suggest that the inability toforcefully elevate pleuroperitoneal pressure is a consequenceof the tadpoles' short and inflexible spine. Although postmetamorphicfrogs have a similarly short vertebral column, they can compressviscera by movement at sacroiliac joints, which are absent intadpoles. I argue that the short torso of tadpoles is a necessaryconsequence of the need to innervate the frog's limbs earlyin development so that they can be fully functional by the endof metamorphosis. The short torso is a good mechanical design for the saltatoryfrog, but afflicts the tadpoles with a distinctly globous shapethat intuitively appears inefficient for aquatic locomotion.Computational fluid dynamics (CFD) models, however, reveal thattadpoles are, in fact, efficient undulatory swimmers comparedto subcarangiform fishes and that their swimming kinematicswork in concert with their shape to help generate thrust. Furthermorethe CFD models show that the crease in the dorsal profile oftadpoles, where the body abruptly meets the tail, produces a"dead water" zone immediately behind the body of the tadpole.As a result, tadpoles can grow hindlimbs in this region withoutthose limbs seriously impeding flow. Thus the shape of tadpolesnicely matches their need to transform into limbed tetrapods. In the latter half of this paper I review ideas on how environmentalfactors could influence metamorphosis in anurans. One speculationis that tadpoles may secrete a metamorphic inhibitor in theiroral mucus, which they then ingest with their food, with theresult that metamorphosis is delayed when food is abundant.An epidermal growth factor-like peptide has been suggested asa possible metamorphic inhibitor along the pathway just proposed.Strengths and weaknesses of this hypothesized agent and pathwayare reviewed. An experiment to test the hypothesis that orallyingested EGF inhibits metamorphosis yielded inconclusive results.Orally secreted EGF-like peptide may not inhibit metamorphosisof the tadpole gut, but other yet-to-be-identified factors intadpole oral mucus could still play a role in regulating metamorphosisof the alimentary tract in anurans. The essay ends with some broad speculations on the role thatpeptides in frogs' skin may play in the metamorphic processas well as several unanswered questions about how other organismsand the physical environment influence tadpole metamorphosis. 相似文献
9.
Martilias S. Farrell John D. McCorvy Xi-Ping Huang Daniel J. Urban Kate L. White Patrick M. Giguere Allison K. Doak Alison I. Bernstein Kristen A. Stout Su Mi Park Ramona M. Rodriguiz Bradley W. Gray William S. Hyatt Andrew P. Norwood Kevin A. Webster Brenda M. Gannon Gary W. Miller Joseph H. Porter Brian K. Shoichet William E. Fantegrossi William C. Wetsel Bryan L. Roth 《PloS one》2016,11(3)
Rationale
The sacred lotus (Nelumbo nucifera) contains many phytochemicals and has a history of human use. To determine which compounds may be responsible for reported psychotropic effects, we used in silico predictions of the identified phytochemicals. Nuciferine, an alkaloid component of Nelumbo nucifera and Nymphaea caerulea, had a predicted molecular profile similar to antipsychotic compounds. Our study characterizes nuciferine using in vitro and in vivo pharmacological assays.Methods
Nuciferine was first characterized in silico using the similarity ensemble approach, and was followed by further characterization and validation using the Psychoactive Drug Screening Program of the National Institute of Mental Health. Nuciferine was then tested in vivo in the head-twitch response, pre-pulse inhibition, hyperlocomotor activity, and drug discrimination paradigms.Results
Nuciferine shares a receptor profile similar to aripiprazole-like antipsychotic drugs. Nuciferine was an antagonist at 5-HT2A, 5-HT2C, and 5-HT2B, an inverse agonist at 5-HT7, a partial agonist at D2, D5 and 5-HT6, an agonist at 5-HT1A and D4 receptors, and inhibited the dopamine transporter. In rodent models relevant to antipsychotic drug action, nuciferine blocked head-twitch responses and discriminative stimulus effects of a 5-HT2A agonist, substituted for clozapine discriminative stimulus, enhanced amphetamine induced locomotor activity, inhibited phencyclidine (PCP)-induced locomotor activity, and rescued PCP-induced disruption of prepulse inhibition without induction of catalepsy.Conclusions
The molecular profile of nuciferine was similar but not identical to that shared with several approved antipsychotic drugs suggesting that nuciferine has atypical antipsychotic-like actions. 相似文献10.
Alexander P. Gultyaev F.H.D. van Batenburg Cornelis W.A. Pleij 《Journal of molecular evolution》2002,54(1):1-8
Comparison of the most stable potential hairpins in the sequences of natural ribozymes with those in the randomized sequences
has revealed that the hairpin loop energies are lower than expected by chance. Although these hairpins are not necessarily
parts of functional structures, there is a selective pressure to diminish the destabilizing free energies of the hairpin loops.
In contrast, no significant bias is observed in the stacking values of the most stable stems. In the ribozymes isolated in
vitro the loops of potential hairpins are closer to random values, which can result in less efficient folding rates. Furthermore,
the effects of kinetic traps seem to be more significant in the folding pathways of the in vitro isolates due to a potential
to form stable stacks incompatible with the functional folds. Similarly to natural ribozyme sequences, the untranslated regions
of viral RNAs also form hairpins with relatively low loop free energies. These evolutionary trends suggest ways for efficient
engineering of improved RNA constructs on the basis of analysis of in vitro isolates and approaches for the search of regions
coding for functional RNA structures in large genome sequences.
Received: 12 January 2001 / Accepted: 21 May 2001 相似文献
11.
Effects of Lead In Vivo and In Vitro on GABAergic Neurochemistry 总被引:2,自引:1,他引:1
Ellen K. Silbergeld Robert E. Hruska Leonard P. Miller Nancy Eng 《Journal of neurochemistry》1980,34(6):1712-1718
Abstract: Alterations in aspects of neurotransmission utilizing -γ-aminobutyric acid (GABA) are associated with in vivo exposure of rats to lead at doses that do not produce convulsions, but sensitize animals to convulsant agents. These effects are observed regionally and include: decreased GABA levels in cerebellum; increased activity of glutamate decarboxylase (GAD) in caudate; and decreased GABA release (both resting and K+ -stimulated) in cortex, caudate, cerebellum and substantia nigra. Sodium-dependent uptake of GABA by synaptosomes of cerebellum, substantia nigra and caudate was also affected: in these regions, affinity (Km ) was increased and maximal velocity (Vmax ) was reduced. Sodium-independent binding of GABA to synaptic membranes was increased in cerebellum, but was observed only when tissue was Tritonized and prepared without freezing and washing. No effects on GAD or on GABA uptake, release, or binding were observed when lead was added to brain tissue in vitro in concentrations as high as 100 μM. The results suggest that lead may produce chronic inhibition of presynaptic GABAergic function, notably in the cerebellum, which is associated with supersensitivity of postsynaptic GABA receptors. Failure of lead to affect GABAergic function in vitro may indicate that these effects are secondary to another neurotoxic action of lead in the CNS or are consequent to a nonneuronal metabolic action of lead. 相似文献
12.
Regulation of Pyruvate Decarboxylase In Vitro and In Vivo 总被引:2,自引:0,他引:2
Results presented in this paper strongly support the view thatregulation of the key enzyme of alcoholic fermentation, pyruvatedecarboxylase (PDC), is achieved in a number of ways, all associatedwith possible lowering of the cytoplasmic pH during anoxia.These mechanisms include not only the well-known acid pH optimumof PDC, but also long-term, reversible changes in characteristicsof the enzyme established both in vitro and in vivo. Following transfer of desalted extracts from pH 6.0 to 7.4,maximal activity of PDC was decreased, while there was a considerableincrease in the lag before maximal activity was reached. Similarchanges in enzyme characteristics were observed when wheat (Triticumaestivum L. cv. Gamenya) roots and rice (Oryza sativa L. cv.Calrose) coleoptiles were transferred from anoxic to aerobicsolutions, provided PDC was assayed within 10 min of the startof maceration. All of the above changes were usually readilyreversible when extracts were returned to pH 6.0, or when plantswere returned to anoxic solutions. Additional regulation of PDC would be achieved by the S0.5 forpyruvate which is 0.75 mol m3 at pH 6.0, 1.0 mol m3at pH 6.8, and 2.5 mol m3 at pH 7.4; the latter is wellabove estimates for pyruvate concentrations in the cytoplasmof aerated tissues. We assess that the combined effects of the acid pH optimum,the high S0.5 at pH 7.4 and the long-term decreases in activityobserved during incubation at pH 7.4 would reduce PDC activityin aerobic cells to at most 7% of the activity in anoxic cells.Possible additional controls for the pathway of alcoholic fermentationare briefly considered. Key words: PDC, regulation, anoxia 相似文献
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Jun‐Hui Choi Yoon‐Sik Kim Chang‐Ho Shin Hyo‐Jeong Lee Seung Kim 《Journal of biochemical and molecular toxicology》2015,29(12):552-558
The objectives of present study were to investigate whether luteolin affects procoagulant proteinase activity and fibrin clot formation and influences thrombosis and coagulation in Sprague–Dawle rats. Luteolin significantly inhibited the enzymatic activity of thrombin and FXa activity by 29.1% and 16.2%. Luteolin also inhibited fibrin polymer formation in turbidity and microscopic analysis using fluorescent conjugate. Coagulation assay of luteolin was found to prolong activated partial thromboplastin time and prothrombin time. Moreover, luteolin protected the development of oxidative stress induced thrombosis in the FeCl3‐induced carotid arterial thrombus model. This study demonstrated that luteolin may be useful by reducing or preventing thrombotic challenge and can help us better understand the antithrombotic action of luteolin. 相似文献
16.
Full-grown ovarian oocytes removed from non-hormone-treated Rana pipiens females exhibit a low level of protein synthesis, the rate of which is dependent upon the ionic environment. The highest rates of protein synthesis in these oocytes are obtained in media containing either a divalent cation (Ca++ or Mg++) or high levels of K+. The dependence of protein synthesis on ionic environment persists through about the first 18-24 hours of maturation (at 18°C). Normal maturation of oocytes in vitro also has specific ionic requirements for the first 24 hours. In this case, the process requires high ionic strength (T/2 = 1.0-1.2) and divalent cations. The kinetics of K+ exchange suggest that K+ exists in the ovarian oocyte in two compartments; one in equilibrium with the exogenous medium and freely exchangeable; the other in equilibrium with the exogenous medium and freely exchangeable; the other in equilibrium with the first internal compartment and only very slowly exchangeable. The slowly exchangeable (bound) compartment contains about 95% of all endogenous K+. In hormone stimulated oocytes, the kinetics of K+ exchange are essentially the same. Oocyte adaptation to ionic environment is discussed as a possible regulatory mechanism during maturation. 相似文献
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Cytoglobin, generated using genetic engineering method, is a kind of recombinant human stellate cell activation-associated
protein. We speculate that it could influence the development of hepatic fibrosis like Sellate cell activation-associated
protein which was discovered by Kawada et al. Therefore, we investigated its anti-fibrosis effect on liver both in vivo and
in vitro. During our research, we found that cytoglobin showed obvious effect compared with the control group on Thioacetamide-induced
liver fibrosis in SD rats, including significantly decrease in aspartate aminotransferase, Hyaluronic acid, laminin and collagen
I(Col I) levels in serum and hydroxyproline in livers, which are the important indices reflecting the degree of hepatic fibrosis.
Meanwhile, the viability of rat hepatic stellate cell line T6 (HSC-T6) cells was inhibited by cytoglobin and the apoptosis
induced by cytoglobin in HSC-T6 cells was detected by Annexin V/PI double staining. Activation of the caspase cascade including
caspase-3 for the intrinsic pathways was demonstrated. The results also showed that the expression of Bcl-2 protein decreased
whereas that of Bax protein increased, leading to an increase of the Bax/Bcl-2 ratio. Our results demonstrated that cytoglobin
exhibited anti-fibrosis activity on livers in vivo and in vitro, involving apoptosis induction. 相似文献
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From 40 discrete mouse tissue culture cell lines examined by electron microscopy or complement fixation, or both, for the presence of detectable virus, one (NCTC 4705), initiated and maintained on chemically defined medium, was chosen for a more extensive study. Virus-like particles (100 to 110 mμ), morphologically similar to previously reported immature and mature C-type leukemia virus particles, were found budding from the plasma membrane and free in the intracellular spaces of cells in tissue culture and in fibrosarcomas resulting from intramuscular implants of these tissue cultures. Complement-fixation tests for group reactive murine leukemia antigens were positive, with titers consistently higher to a broadly reactive anti-serum than to anti-Friend, anti-Moloney, or anti-Rauscher sera. The 4705 virus was neutralized by Gross antiserum, but not by the F-M-R antisera. When injected into DD, BALB/c, or C3H/He newborn mice, the virus thus far has manifested no leukemogenicity, though virus from tumor extracts and tissue culture medium has been shown to be capable of infecting C3H and Swiss mouse embryo tissue cultures and successfully replicating in them. The role of the virus in accelerating or inducing neoplastic transformation in NCTC 4705 is still not known. When it was introduced into NCTC [ill], a non-neoplastic cell line in other respects similar to NCTC 4705, 4823 manifested no signs of neoplastic transformation after harboring the virus more than 300 days in vitro. 相似文献