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    ESTRUCTURACION DE PROYECTO OPIOID IN SHRIMP

    An opioidis any chemical that resembles morphineor other opiatesin its

    pharmacological efects. Opioids work by binding to opioid receptors, which

    are ound principally in the centraland peripheral nervous systemand the

    gastrointestinal tract. The receptors in these organ systems mediate thebenecial efects as well as the psychoactiveand the side efectso opioids.

    Opioid receptorsare a group o G proteincoupled receptorswith opioids

    as ligands. The endogenous opioids are dynorphins, enkephalins,

    endorphins, endomorphins and nociceptin. The opioid receptors are !"#$

    identical to somatostatin receptors%&&T's(. Opioid receptors are distributed

    widely in the brain, and are ound in the spinal cordand digestive tract.

    G proteincoupled receptors %GPCRs(, also known as seven-

    transmembrane domain receptors, 7TM receptors, heptahelical

    receptors, serpentine receptor, and G proteinlinked receptors%GPLR(, constitute a large proteinamily o receptorsthat sense molecules

    outside the cell and activate inside signal transduction pathways and,

    ultimately, cellular responses. They are called seventransmembrane

    receptors because they pass through the cell membrane seven times.)*

    G proteincoupled receptors are found only in eukaryotes, including yeast,

    choanoflagellates,[2]and animals. The ligandsthat bind and activate these receptors

    include light-sensitive compounds, odors,pheromones, hormones, and

    neurotransmitters, and vary in sie from small molecules topeptidesto largeproteins. G

    proteincoupled receptors are involved in many diseases, and are also the target ofappro!imately "#$ of all modern medicinal drugs.[%]["]The 2#&2'obel (rie in

    )hemistry*as a*arded to +rian obilkaand obert efko*itfor their *ork that *as

    /crucial for understanding ho* G proteincoupled receptors function./.[0]There have

    been at least seven other'obel (riesa*arded for some aspect of G protein-mediated

    signaling.

    There are t*o principal signal transduction path*ays involving the G proteincoupled

    receptors1

    the c3(signal path*ay and

    thephosphatidylinositolsignal path*ay.[4]

    5hen a ligand binds to the G() it causes a conformational change in the G(),

    *hich allo*s it to act as a guanine nucleotide e!change factor6G789. The G() can

    then activate an associatedG proteinby e!changing its bound G:(for a GT(.The G

    protein;s < subunit, together *ith the bound GT(, can then dissociate from the = and >

    subunits to further affect intracellular signaling proteins or target functional proteins

    directly depending on the < subunit type 6G

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    +lassication

    +lassication &cheme o G+'s. +lass A %'hodopsinlike(, +lass - %&ecretin

    like(,+lass + %Glutamate 'eceptorlike(, Others %Adhesion %**(, ri//led %00(,

    Taste type1 %12(, unclassied %1*((.345

    The e!act sie of the G() superfamilyis unkno*n, but nearly A## different human

    genes6or B"$ of the entireprotein-codinggenome9 have been predicted from genome

    se@uence analysis.[A]lthough numerous classification schemes have been proposed, the

    superfamily *as classically divided into three main classes 6, +, and )9 *ith no

    detectable shared se@uence homologybet*een classes.

    The largest class by far is class , *hich accounts for nearly A0$ of the G() genes.

    Cf class G()s, over half of these are predicted to encodeolfactory receptors, *hile

    the remaining receptors are ligandedby kno*n endogenouscompoundsor are classified

    as orphan receptors. :espite the lack of se@uence homology bet*een classes, all G()s

    have a common structureand mechanism of signal transduction. The very large

    rhodopsin group has been further subdivided into &D subgroups 6&-&D9.[D]

    3ore recently, an alternative classification system called G8E 6Glutamate,

    hodopsin, dhesion, 8riled?Taste2,Eecretin9 has been proposed.[A]

    +y this system,G()s can be grouped into 4 classes based on se@uence homology and functional

    similarity1[][&&][&2][&%]

    +lass A %or 0( %'hodopsinlike(

    +lass - %or 1( %&ecretin receptor amily(

    +lass +%or *( %6etabotropic glutamate7pheromone(

    +lass 8 %or "( %ungal mating pheromone receptors(

    +lass 9 %or 2( %+yclic A6 receptors(

    https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-pmid16753280-8https://en.wikipedia.org/wiki/Superfamily_(molecular_biology)https://en.wikipedia.org/wiki/Humanhttps://en.wikipedia.org/wiki/Geneshttps://en.wikipedia.org/wiki/Protein_biosynthesishttps://en.wikipedia.org/wiki/Genomehttps://en.wikipedia.org/wiki/Genomehttps://en.wikipedia.org/wiki/Sequence_analysishttps://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-pmid16753280-8https://en.wikipedia.org/wiki/Sequence_homologyhttps://en.wikipedia.org/wiki/Olfactory_receptorshttps://en.wikipedia.org/wiki/Olfactory_receptorshttps://en.wikipedia.org/wiki/Ligand_(biochemistry)https://en.wikipedia.org/wiki/Ligand_(biochemistry)https://en.wikipedia.org/wiki/Endogenoushttps://en.wikipedia.org/wiki/Endogenoushttps://en.wikipedia.org/wiki/Chemical_compoundhttps://en.wikipedia.org/wiki/Orphan_receptorhttps://en.wikipedia.org/wiki/Protein_tertiary_structurehttps://en.wikipedia.org/wiki/Signal_transductionhttps://en.wikipedia.org/wiki/Rhodopsin-like_receptors#Classeshttps://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-9https://en.wikipedia.org/wiki/Metabotropic_glutamate_receptorhttps://en.wikipedia.org/wiki/Rhodopsinhttps://en.wikipedia.org/wiki/Frizzledhttps://en.wikipedia.org/wiki/Taste_receptorhttps://en.wikipedia.org/wiki/Taste_receptorhttps://en.wikipedia.org/wiki/Secretin_receptorhttps://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-pmid16753280-8https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-pmid16753280-8https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-10https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-11https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-12https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-13https://en.wikipedia.org/wiki/Rhodopsin-like_receptorshttps://en.wikipedia.org/wiki/Secretin_receptor_familyhttps://en.wikipedia.org/wiki/Class_C_GPCRhttps://en.wikipedia.org/wiki/Metabotropic_glutamate_receptorhttps://en.wikipedia.org/wiki/Fungal_mating_pheromone_receptorshttps://en.wikipedia.org/wiki/Cyclic_AMP_receptorshttps://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-pmid16753280-8https://en.wikipedia.org/wiki/Superfamily_(molecular_biology)https://en.wikipedia.org/wiki/Humanhttps://en.wikipedia.org/wiki/Geneshttps://en.wikipedia.org/wiki/Protein_biosynthesishttps://en.wikipedia.org/wiki/Genomehttps://en.wikipedia.org/wiki/Sequence_analysishttps://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-pmid16753280-8https://en.wikipedia.org/wiki/Sequence_homologyhttps://en.wikipedia.org/wiki/Olfactory_receptorshttps://en.wikipedia.org/wiki/Ligand_(biochemistry)https://en.wikipedia.org/wiki/Endogenoushttps://en.wikipedia.org/wiki/Chemical_compoundhttps://en.wikipedia.org/wiki/Orphan_receptorhttps://en.wikipedia.org/wiki/Protein_tertiary_structurehttps://en.wikipedia.org/wiki/Signal_transductionhttps://en.wikipedia.org/wiki/Rhodopsin-like_receptors#Classeshttps://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-9https://en.wikipedia.org/wiki/Metabotropic_glutamate_receptorhttps://en.wikipedia.org/wiki/Rhodopsinhttps://en.wikipedia.org/wiki/Frizzledhttps://en.wikipedia.org/wiki/Taste_receptorhttps://en.wikipedia.org/wiki/Secretin_receptorhttps://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-pmid16753280-8https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-10https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-11https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-12https://en.wikipedia.org/wiki/G_protein-coupled_receptor#cite_note-13https://en.wikipedia.org/wiki/Rhodopsin-like_receptorshttps://en.wikipedia.org/wiki/Secretin_receptor_familyhttps://en.wikipedia.org/wiki/Class_C_GPCRhttps://en.wikipedia.org/wiki/Metabotropic_glutamate_receptorhttps://en.wikipedia.org/wiki/Fungal_mating_pheromone_receptorshttps://en.wikipedia.org/wiki/Cyclic_AMP_receptors
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    +lass %or :( %ri//led7&moothened(

    The human genome encodes thousands of G protein-coupled receptors,[&"]about %0# of

    *hich detect hormones, gro*th factors, and other endogenous ligands. ppro!imately

    &0# of the G()s found in the human genome have unkno*n functions.

    Eome *eb-servers[&0]and bioinformatics prediction methods[&4][&F]have been used for

    predicting the classification of G()s according to their amino acid se@uence alone, by

    means of thepseudo amino acid compositionapproach.

    NOREPINEPHRINE

    Norepinephrine6''9 6abbreviated norepior NE9, also called noradrenaline6+'9

    6abbreviated NA, NAd, or norad9, or 4,5!"rih#dro$#phene"h#la%ineis a

    catecholamine*ith multiple roles including those as a hormoneand a neurotransmitter.[&]t is the hormone and neurotransmitter most responsible for vigilantconcentrationin

    contrast to its most chemically similar hormone, dopamine, *hich is most responsible

    for cognitivealertness.[2]

    Norepinephrine reulates prophenolo!idase s"stem-related

    parameters and ene e!pressions via #- and $-adreneric

    receptors in Litopenaeus vannamei%http&''(((%ncbi%nlm%nih%ov'pubmed'))*7+,.

    +O;+O;? These results suggest that stressinduced ;9 may promote

    the migration o circulating granulocytes to the site o the in@ection and the

    e)isting proO m';A translation which had been stored in granulocytes. ;9

    downregulated the , proO>>, &, and 9 gene transcription by

    haemocytes via 0, B0, 0, 0 and B0, and 0 and B0A's, respectively,

    which subseCuently decreased the O activity by 0 and B0A's in

    haemocytes o

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    central nervous system%+;&( o animals, including humans. >t is popularly

    thought to be a contributor to eelings o wellbeing and happiness.

    Molecular clonin and 0unctional e!pression o0 the

    Penaeus monodon 1-2T receptor%Ongvarrasopone +0, 'oshorm F, &omyong &, othiratana +, etchdee &,

    Tangkhabuanbutra , &ophasan &, anyim &.

    5uthor in0ormation

    5bstract

    Eerotonin 60-HT9 mediates a number of diverse physiological functions in crustaceans

    by interacting *ith various 0-HT receptor subtypes. putative 0-HT receptor cloned

    from the ovary of the black tiger pra*n 6(enaeus monodon9 consisted of 22D&

    nucleotides, encoding a putative 0-HT6&(em9 receptor protein of 0D& amino acids.Transient e!pression of 0-HT6&(em9 in H72D% cells demonstrated a saturable [%H]-0-

    HT binding *ith a d of ."%I?-&.&% n3 and +ma! of &.0%I?-#.#4 pmol?mg. The

    putative 0-HT6&(em9 receptor is e!pressed in all tissues e!amined and is constitutively

    e!pressed in the ovary during ovarian maturation and spent phase. (olyclonal antibodies

    against the third intracellular loop 6i% loop9 of the 0-HT receptor sho*ed that the 0-

    HT6&(em9 receptor protein *as e!pressed in the trabeculae of ovarian stages & and 2

    but on the cortical rod and surrounding the oocyte membrane of stages % and ",

    suggesting that receptor localiation plays a critical role in regulating ovarian

    maturation and spa*ning in penaeus shrimp.

    JJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJ

    Clonin o0 opioid receptors in common carp

    6C"prinus carpio L% and their involvement in

    reulation o0 stress and immune response%+had/inska 60, Hermsen T, &avelkoul H, Ierburgvan Jemenade -6.

    5uthor in0ormation

    5bstract

    n mammals opiate alkaloids and endogenous opioid peptides e!ert their physiological

    and pharmacological actions through opioid receptors 63C, :C and C9

    e!pressed not only on neuroendocrine cells but also on leukocytes. Therefore, opioids

    can modulate the immune response. 5e cloned and se@uenced all three classical opioid

    receptors 63C, :C and C9 in common carp, and studied changes in their

    e!pression during stress and immune responses. 3essenger ' of opioid receptors

    *as constitutively e!pressed in brain areas, specially in the preoptic nucleus '(C

    6homologous to mammalian hypothalamus9. fter e!posure to prolonged restraintstress, m' levels of 3C and :C decreased in the '(C and in the head kidney.

    http://en.wikipedia.org/wiki/Central_nervous_systemhttp://en.wikipedia.org/wiki/Happinesshttp://www.ncbi.nlm.nih.gov/pubmed?term=Ongvarrasopone%20C%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Roshorm%20Y%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Somyong%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Pothiratana%20C%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Petchdee%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Tangkhabuanbutra%20J%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Sophasan%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Panyim%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed/16949686http://www.ncbi.nlm.nih.gov/pubmed/?term=Chadzinska%20M%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/?term=Hermsen%20T%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/?term=Savelkoul%20HF%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/?term=Verburg-van%20Kemenade%20BM%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/18977430http://en.wikipedia.org/wiki/Central_nervous_systemhttp://en.wikipedia.org/wiki/Happinesshttp://www.ncbi.nlm.nih.gov/pubmed?term=Ongvarrasopone%20C%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Roshorm%20Y%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Somyong%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Pothiratana%20C%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Petchdee%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Tangkhabuanbutra%20J%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Sophasan%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed?term=Panyim%20S%5BAuthor%5D&cauthor=true&cauthor_uid=16949686http://www.ncbi.nlm.nih.gov/pubmed/16949686http://www.ncbi.nlm.nih.gov/pubmed/?term=Chadzinska%20M%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/?term=Hermsen%20T%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/?term=Savelkoul%20HF%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/?term=Verburg-van%20Kemenade%20BM%5BAuthor%5D&cauthor=true&cauthor_uid=18977430http://www.ncbi.nlm.nih.gov/pubmed/18977430
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    ncreased e!pression of all studied opioid receptors *as observed in the pituitary pars

    distalis 6containing )TH-producing cells9. n immune organs, constitutive but lo*er

    e!pression of opioid receptor genes *as observed. :uring in vivo ymosan-induced

    peritonitis or after in vitro (E-induced stimulation, *hen pro-inflammatory functions

    are activated, e!pression of the C genes in leukocytes *as concomitantly up-

    regulated. dditionally, specific agonists of opioid receptors especially reduced

    leukocyte migratory properties, manifested by reduced chemota!is and do*n-regulated

    e!pression of chemokine receptors. Cur data indicate an evolutionary conserved role for

    the opioid system in maintaining a dynamic e@uilibrium *hile coping *ith stress and?or

    infection.

    http&''(((%ncbi%nlm%nih%ov'pubmed'+.*77,8