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1.
Monooxygenase reactions catalyzed by cytochromes P-450 are paramount in the oxidative metabolism of many xenobiotics, determining both the persistence and effects of numerous types of compounds. Immunological probes are proving useful in evaluating the functions of P-450 isozymes in microsomal preparations from many species. The regulation of specific isozymes by endogenous and exogenous factors can also be evaluated with such probes. Here we describe studies on the activities apparently catalyzed by induced P-450 in fish, evaluated with both polyclonal and monoclonal antibodies to cytochrome P-450E, the apparent major β-naphthoflavone(BNF) or methylcholanthrene(MC)-inducible isozyme purified from scup (S. chrysops) liver.  相似文献   

2.
The hepatic mixed function oxidase system in the fish differs from that in mammals in its responses to the two classic mammalian inducers. The cytochrome P-448-type inducers (polycyclic aromatic hydrocarbons) stimulate monooxygenase activity, but phenobarbital, a P-450-type inducer, does not.1 We have compared the effects of phenobarbital (PB) and polychlorinated biphenyls (PCB) on the turnover of hepatic microsomal hemoproteins in trout (PCB's are P-448- and P-450-type inducers in mammals, which in fish induce only cytochrome P-448). We show here that neither PCB nor PB treatment changed the turnover rate. However, both the rates of synthesis and degradation were much slower than in the rat.  相似文献   

3.
Cytochrome P450 monooxygenases constitute an enzyme superfamily, with at least 74 known families. Members of CYP families 1–4 are important in the phase 1 metabolism of lipophilic xenobiotics, such as those found in contaminated marine environments. Previous studies (James et al. Arch. Biochem. Biophys. (1996) 329, 31–38) showed that a major form of P450 in spiny lobster, Panulirus argus, hepatopancreas was CYP2L1, a new sub-family, and that there was evidence for other P450 forms in hepatopancreas. We now report the sequence of a second member of this subfamily, named CYP2L2, present in P. Argus hepatopancreas. The deduced amino acid sequences of CYP2L1 and CYP2L2 share 54.7% sequence identity and an additional 13.6% of the sequences show conservative substitutions. Analysis of the sequences of CYP2L1, CYP2L2 and other representative CYP2 family members (from rat and mouse sub-families 2A, 2B, 2D and 2E) showed that the crustacean sequences clustered together. In addition to CYP2L2, cDNA clones of 66 to 117 base pairs from the 5′ coding region of two more P450 isoforms were isolated from the spiny lobster cDNA library. The deduced amino acid sequence of one of these additional cDNA clones was identical to the first 22 amino acids of the N-terminal sequence of a P450 protein previously isolated from hepatopancreas microsomes. These studies confirm earlier biochemical evidence that the hepatopancreas contains multiple forms of cytochrome P450.  相似文献   

4.
The effects of the mammalian inhibitor ellipticine (5,11-dimethyl-[6H]-pyrido[4,3b] carbazole) were examined in a mechanistic study of the cytochrome P450 monooxygenase system of control and β-naphthoflavone (βNF)-induced hepatic microsomes of Platichthys flesus. Ellipticine was indicated to bind to the haem moiety of cytochrome P450s (gave type II binding spectra) and to inhibit the transfer of electrons from both the hydrophobic binding site of cytochrome P450 reductase (P450R) to P450 (inhibited P450R reductase activity) and the hydrophilic binding site of P450R to soluble electron acceptors (inhibited NAD(P)H-cytochrome c reductase activity). No effect was seen on cytochrome b5 reductase activity. Ellipticine inhibition indicated the involvement of (i) P450R (possibly also P450s) in NADPH- but not NADH- dependent hydroxyl radical production, and (ii) electron transfer and P450/P450R interaction in NADPH-dependent cytochrome P450 1A-catalysed monooxygenation (7-ethoxyresorufin O-deethylase activity and benzo(a)pyrene (BaP) metabolism). Differential effects of ellipticine on cumene hydroperoxide (CHP)-dependent BaP metabolism (P450 peroxidase activity) with CHP concentration indicated the existence of at least two forms of P450 with different substrate affinities for CHP, and different mechanisms of formation for protein adducts and free metabolites. Overall, the studies indicate the primary site of action of ellipticine in P. flesus is binding between Fe3+-P450 and P450R.  相似文献   

5.
The capacity of the mammalian liver microsomal P-450-dependent systems to metabolize a wide variety of endogenous and exogenous compounds is thought to reflect the presence of multiple forms of P-450 haemoproteins with broad and overlapping substrate specificity. In plants, the functions and specificity of cytochrome P-450 systems are less well known.This study was designed to prepare and characterize subcellular fractions from fresh sheaths (basal parts of leaves) of a mediterranean seagrass Posidonia oceanica (Linnaeus) Delile, the aim being the preparation of a microsomal fraction suitable for studying xenobiotic metabolism. The purity of the different fractions obtained by centrifugation, as well as the recovery of different organelles, was determined using enzyme markers (cytochrome c oxidase, alkaline phosphatase, glucose-6-phosphatase) and morphological examination by transmission electron microscopy. Some assays of enzymes involved in xenobiotic metabolism (cytochrome c reductase, laurate hydroxylase, ethoxyresorufin O-deethylase and glutathione-S-transferase) were also performed on different fractions of the preparation. The subcellular distribution for drug metabolism and marker enzymes showed a loss of endoplasmic reticulum in the pellet obtained after the first centrifugation, but the microsomal fraction was relatively free of mitochondria and fragments of the plasma membrane.Some assays are still being performed to avoid the small loss of endoplasmic reticulum experienced with the first pellet. However, the microsomes prepared in this study from sheaths of Posidonia oceanica appear suitable for further investigation of xenobiotic metabolism.  相似文献   

6.
The degree of induction of hepatic mixed function oxidase (MFO) enzymes in fish is modulated by environmental conditions. This study was designed to investigate the influence of water temperature, presence or absence of food, and exposure to benzo(a]pyrene (BaP) on the inductive response of bluegill sunfish (Lepomis macrochirus). The results show an increase in 7-ethoxyresorufin O-deethylase (EROD) activity with an increase in acclimation temperature and dose. This activity appears to be associated with a very small fraction of the total cytochrome P-450 induced. Major changes were observed in the 53- and 57-kilodaltons (kDa) electrophoretic bands.  相似文献   

7.
The hepatic microsomal monooxygenase system of fish-eating sea birds has received little attention considering the vulnerability of this group of animals to environmental pollution. Knight et al.1 measured monooxygenase activities of six species of fish-eating sea birds towards the organochlorine pesticide aldrin and the dieledrin analogue HCE (1,2,3,4,9,9-hexachloro-1,4,4a,5,6,7,8,8a-octohydro-exo-7,8-epoxy-1,4-methanonaphaline) and found very low activities in all species except the puffin (Fratercula arctica), activities more comparable to those of the fish than those of terrestrial birds. The aims of the present study were to compare the aldrin epoxidase and HCE hydroxylase systems of the razorbill (Alca torda) and the puffin with those of the male rat. Kinetics of the two reactions were compared at substrate concentrations down to environmentally realistic levels and the forms of cytochrome P-450 of the birds were partially characterised and compared with forms equivalently from untreated male rat liver.  相似文献   

8.
The relationship between cytochrome P450 and feeding on terpenoid-rich gorgonian corals was investigated in a species of tropical butterflyfish and compared with two other sympatric congeners that do not feed on gorgonians. Fish were collected from non-polluted waters in Belize and the levels of two cytochrome P450 isozymes (CYP2B and CYP3A) were immunoquantitated in addition to quantification of total P450. Chaetodon capistratus regularly feeds on gorgonian corals and has higher levels of total hepatic microsomal cytochrome P450 than C. ocellatus or C. striatus. The content of hepatic P450 (0.588–0.794 nmol mg−1) in C. capistratus is among the highest ever reported in teleosts from non-polluted waters and is significantly greater than detected in C. ocellatus or C. striatus. Chaetodon capistratus also had a larger hepatic index (g liver per g fish) and more microsomal protein (mg protein per g liver), factors that translate into 3.3- to 8-fold more total P450 per g fish. Sexual differences in total P450 were observed between male and female C. capistratus, but not among the other species. The contents of proteins detected by immunoassay with polyclonal anti-scup P450B (CYP2B) and anti-human P4503A (CYP3A) were 2- to 10-fold and 2- to 20-fold greater, respectively, in C. capistratus than in the congeneric species. CYP2 and CYP3 gene families in mammals are thought to have evolved partially in response to dietary allelochemicals. These results suggest that these P450 isozymes may also be important in marine teleosts that feed on terpenoid-rich prey.  相似文献   

9.
Monoclonal antibody directed against a major β-naphthoflavone (BNF)-induced form of teleost cytochrome P-450, P-450E (equivalent to P-450c in rat) was used to immunolocalize this enzyme in liver, gill and heart of scup and trout. Liver sections from both species showed P-450E in the cytoplasm of hepatocytes. No regional differences were observed which might indicate zonation of cytochrome P-450E within subpopulations of hepatocytes. Scup exocrine pancreatic cells were only weakly positive. In the gill of both fish, cytochrome P-450E was restricted to the endothelium (pillar cells) of secondary lamellae, where fluorescence appeared as a chain in longitudinal sections through lamellae and as star-shaped clusters in en face views. Sections of ventricular wall in both species revealed P-450E was restricted to endothelium at margins of muscle bands limiting heart ventricular lumen. Localization in the specific cells of these and other organs may be fundamentally important in understanding the role of cytochrome P-450E.  相似文献   

10.
Bivalve and gastropod molluscs readily accumulate polynuclear aromatic (PNAH) and other hydrocarbons from the environment and are widely used in environmental monitoring programmes.1 The response of the cytochrome P-450 monooxygenase or mixed function oxidase (MFO) system to organic xenobiotics is of interest from the comparative viewpoint and in biological effects monitoring.2 We have studied the bivalves Mytilus edulis (mussel) and Cardium edule (cockle) and the gastropod Littorina littorea (periwinkle) exposed to hydrocarbons, experimentally or naturally in the field. The general trend of response in digestive gland microsomes was an increase in cytochrome P-450 content and NADPH-cytochrome c reductase (NADPH-CYTCRED) activity but no increase in benzo[a]pyrene hydrolyase (BPH) activity. Sex and seasonal interactions were evident. We conclude that aspects of the responses may be peculiar to the Mollusc and that NADPH-CTYCRED possibly offers potential for this phylogenetic group as a specific indicator of biological impact by organic pollution.  相似文献   

11.
The metabolism of some xenobiotics can lead to the formation of reactive intermediates with mutagenic/carcinogenic properties. With the carcinogenic PAH these have been identified as bay-region diol-epoxides.1 Phenanthrene, a non-carcinogenic, bay-region containing model PAH, is metabolised in vivo by bony fish at the proximate bay-region position, whereas mammals and other marine organisms mainly form the K-region metabolite 9,10-dihydro-9,10-dihydroxy-phenanthrene.2 We wanted to investigate this difference more closely by studying the regiospecificity of phenanthrene metabolism in vitro both with microsomes from differently pretreated cod and with isolated cytochrome P-450 isozymes from BNF-induced cod.3 Secondly, by preparing antibodies to the major isozyme isolated (called cod P-450c), we investigated the immunochemical properties of the variously treated cod liver microsomes.  相似文献   

12.
The incidence of hepatoma, epidermal and other forms of cancerous growths in fish is well documented (Halver, 1967; Matsushima & Sugimura, 1976; Dawe et al., 1964). In fish, as in mammals, cancer may be a result of metabolically activated carcinogens. In mammals the primary enzyme system involved in the activation of environmental carcinogens is the cytochrome P-450 linked mixed-function oxidase (MFO). The hepatic microsomes of the species offish studied contain variable levels of cytochrome P-450. Liver microsomes of the trout Salmo trutta lacustris are surprisingly active in metabolising benzo-[a]pyrene (BP) and other compounds preferentially metabolised by polycyclic aromatic hydrocarbon (PAH)-specific cytochrome P-450. This finding may be significant, because it is apparent that the detrimental effects of PAHs require metabolic activation.We have studied the production of reactive intermediates of BP by following their binding to DNA and by measuring the specific nucleotide-BP metabolite complexes by chromatography. Untreated S. trutta liver microsomes catalyse the production of reactive intermediates of BP which bind to nucleotides of DNA at a rate that is 3–4 times higher than that catalysed by control rat liver microsomes. The most prominent DNA-BP metabolite adducts produced by trout liver microsomes are the nucleoside adduct of BP-7, 8-diol-9,10-epoxide and 9-OH-BP-4,5-oxide and other phenol oxides. In contrast to the trout, another fish species, roach (Rutilus rutilus), has extremely low activity. Although the in vitro binding of BP to DNA is not strictly correlated to in vivo binding or biological effects, our results show that reactive intermediates are formed by trout liver and thus the prerequisite for chemical carcinogenesis or mutagenesis is ful filled. This is further supported by the fact that in Ames's test, trout liver preparations produce mutagenic products from promutagens.  相似文献   

13.
Cytochrome P-450 monooxygenases catalyze the biotransformation of a great variety of foreign, as well as endogenous, lipid-soluble compounds to more water-soluble products. As in mammals, highest concentration of cytochrome P-450 in fish is found in the liver. However, previous studies have indicated that fish kidney contains relatively high cytochrome P-450-mediated activities.1,2 We have therefore prepared and characterized subcellular fractions from the kidney of rainbow trout suitable for studies on cytochrome P-450-dependent reactions. Furthermore, as in the liver, several cytochrome P-450-mediated reactions in the kidney were induced following treatment of the fish with β-naphthoflavone.  相似文献   

14.
The monooxygenase cytochrome P-450 is a ubiquitous enzyme well known for its role in the detoxication of drugs and xenobiotics and the biosynthesis of the steroid hormones. The toxicity and carcinogenicity of many chemicals is frequently due to the formation of oxygenated reactive intermediates, which are formed by the same enzymes that effect the detoxication of these chemicals, namely the cytochromes P-450. In mammalia the cytochromes P-450 exist as a group of isoenzymes with overlapping substrate affinities, selectively and differentially induced by their specific substrates or inhibitors. As few enzyme assays have been shown to be specific for a particular cytochrome P-450 isoenzyme the characterisation of these isoenzymes has been dependent on their isolation and purification. It is therefore important to know whether one or more isoenzyme of cytochrome P-450 is specifically concerned with the activation of carcinogens and chemicals, rather than their detoxication, and to develop a specific enzymic assay for this activating enzyme.  相似文献   

15.
The development of an effective artificial larval diet has been a major stumbling block for advancing the aquaculture of spiny lobsters internationally. Attempts to determine the natural diet of spiny lobster larvae have been impeded by their small size and sparse distribution in the open ocean, making these larvae difficult to study using conventional methods. Recent advances in molecular genetic techniques have provided a novel route for identifying the natural prey of spiny lobster larvae (phyllosoma). In this study, sequences from zooplankton found associated with phyllosomas, along with sequences from GenBank, were used to design a suite of group-specific primers. These primers were able to amplify via the polymerase chain reaction (PCR) a short (100–200 base pair) DNA fragment from the 16S or COI locus of potential prey but not from lobster. These methods were applied to four wild-caught phyllosomas of Jasus edwardsii and two phyllosomas of Scyllarus sp. Z. Gadiforme, Cnidaria, Gastropoda and Decapoda crustacean (non-lobster) DNA sequences were obtained from the gut contents of these lobster larvae and inferred as prey. These initial results confirm previous studies using other less definitive methods which have indicated that phyllosomas are opportunistic predators of a wide range of zooplankton taxa.  相似文献   

16.
Based on the assumption that depleted stocks would have recovered during a six-year layoff from fishing, trapping for deep-water spiny lobster Palinurus delagoae and slipper lobster Scyllarides elisabethae off eastern South Africa resumed in 2004 until 2007. A generalised linear modelling approach was used to investigate the effects of year, sampling area, depth, month and trap soak-time on catch and lobster size, and to construct standardised abundance indices. The renewed trapping rapidly reversed partially restored nominal catch rates. Fishing strategy changed from targeting spiny lobsters during the first months of each fishing season to targeting slipper lobsters during later months. Small spiny lobsters were abundant in the southern area, identified as a recruitment hotspot. Spiny lobster abundance and size in this area increased over four years of fishing, but conversely, large adult spiny lobsters predominated in the central and northern areas, where trapping depleted their abundance over time. The adult populations in the central and northern areas are upstream from the recruitment hotspot, and are presumably a source of larvae. Slipper lobster abundance peaked in 2005, remained relatively constant across areas, and increased with depth. Trapping for deep-water lobster is unlikely to be sustainable in its present form. However, the clear gradients in spiny lobster size and abundance by sampling area and depth provide a good framework for spatial management planning.  相似文献   

17.
The spiny lobster Jasus edwardsii (Hutton) supports a thriving new fishery at the Chatham Islands, about 770 km east of New Zealand. Commercial fishing for J. edwardsii started in November 1965, and within 2 years the area became a major centre of New Zealand's large spiny lobster fishery, which earned >NZ$5,000,000 in 1967. Over 12 months (September 1966 to August 1967) landings at the Chatham Islands made up 39.8% of the total New Zealand spiny lobster catch of 16,600,0001b.

In the first year of fishing 2,177,923 lb of spiny lobsters were caught, and in the second 7,129,658lb—a 227% increase. Fishing effort also increased substantially: average number of boats fishing each month rose by 174% in the second year, and the total number of boat‐fishing days by 152%. Most specimens of J. edwardsii caught are large and mature, typical of a virgin stock.  相似文献   

18.
Increasing anthropogenic pollution of the environment can have adverse consequences for organisms which are more subtle than direct toxicity. Detectable levels of persistent pollutants remain even if the substance is no longer used. An example is atrazine, a herbicide in common use throughout the world but one which has been banned in Germany since 1992. As a lipophilic substance, atrazine is bioconcentrated which may lead to chronic intoxication or physiological stress. In order to withstand chemical stressors, many organisms possess detoxication enzymes, for example certain P-450 monoxygenases and glutathione S-transferases. But detoxication demands cellular energy, and in developing organisms, such as fish embryos which have particularly high energy needs for sustaining growth and organogenesis, the additional energy needs of detoxication may present additional stress. In this study, uptake of atrazine, cytochrome P-450 binding spectra, effects on microsomal and soluble glutathione S-transferase activities, and the initial detoxication steps of atrazine via microsomal and soluble glutathione S-transferases were studied using early life stages of zebrafish.  相似文献   

19.
In this study we have used cloned gene probes for human glutathione peroxidase (GPX), rat cytochrome P-450IVA1 and rat cytochrome P-450IIE1 to detect homologous sequences in RNA from the hepato-pancreas of Mytilus edulis. The presence of sequences hybridising to the GPX and P-450IVA1 probes, but not to the P-450IIE1 probe, confirms the ancient origin of the former genes and indicates that conserved-sequence DNA probes from higher organisms can be used to examine the structure and function of genes of environmental interest in marine organisms.  相似文献   

20.
Purification of cytochromes P-450 from liver microsomes of β-naphthoflavone (BNF)-fed rainbow trout yielded three apparently homogeneous forms. The major form (LM4b)* appears to be a P-448 type of cytochrome. A minor form (LM4a), having properties very similar to LM4b, was also obtained. In addition, a P-450 form (LM2) was isolated, with properties quite different from LM4a or LM4b, including a high rate of aflatoxin B1 (AFB1) metabolism (Williams & Buhler, 1983c). Antibodies to all three forms were obtained from rabbits. The IgGs prepared against LM4a and LM4b both cross-reacted (forming lines of identity) equally well with both antigens on Ouchterlony plates. Rat P-448 cross-reacted (without lines of identity) with both LM4a- and LM4b-IgG. LM4b-IgG was much more effective than LM4a-IgG for inhibition of LM4a or LM4b reconstituted benzo[a]pyrene (BP) hydroxylase, suggesting that these two antibodies recognize different antigenic sites. The LM2-IgG did not cross-react with any of the other rat or trout cytochromes P-450 examined. Levels of LM2 and LM4b in microsomes from untreated, polychlorinated biphenyl (PCB), phenobarbital (PB) or BNF-treated trout were estimated with an immunological technique involving electrophoresis on SDS-PAGE, followed by transfer to nitrocellulose and staining with either LM 2 - or LM4b -IgG. The ratio of in microsomes from PCB- or BNF-treated rainbow trout was much higher than 1, whereas the reverse was true with microsomes from untreated rainbow trout. These results are consistent with previous observations (Vodicnik et al., 1982) that pretreatment with BNF induced the synthesis of a P-448 type cyytochrome, presumably responsible for the great increase in the metabolism and activation of BP seen in these fish. Conversely, pretreatment with PB did not affect the levels of either LM2 or LM4b. This specific immunological technique should make it possible to assay the levels of these P-450 and P-448 isozymes in various strains of rainbow trout and other species of fish. In addition, the effect of age, sex, diet and exposure to P-450 and P-448 inducers could be examined and, perhaps, utilized to predict the relative risk of certain populations to pollutants activated by these different isozymes.  相似文献   

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