Age Affects Drug Metamorphosis Essays

Age Affects Drug Metamorphosis Essays Age Affects Drug Metamorphosis Essay Age Affects Drug Metamorphosis Essay Introduction There has been a batch of work and research carried out since the find that age affects drug metamorphosis which can take to toxicity in the 1950s and 1960s. Therefore more cognition and understanding about how drug metamorphosis affects age is critical, which led to the happening out of the of import function of the liver, cytochrome enzyme household, genetic sciences and transporter systems in drug metamorphosis. Age was discovered to hold singular consequence on most of this phenomena involved in drug metamorphosis such as liver volume decrease, lessening in activity of some cytochrome enzymes household. However, the job of acquiring healthy liver tissue of homo and some limitation ethically have limited the surveies of drug metamorphosis effects on age in relation to toxicity. There are legion factor that besides influence the toxicokinetics of drugs in homo. Adult population have more advantage in footings of surveies affecting drugs metamorphosis than the older population and p ediatric population due to hazards involved and ethical grounds in surveies on new drugs which discourage testing of drugs in the older and pediatric population. Changes in drug metamorphosis may be due to differences in toxicokinetics which include soaking up, distribution, metamorphosis or elimination. There are legion variety meats and system that diminution with age and besides undeveloped variety meats and systems in babies or pediatricss affects drug metamorphosis has consequence of this conditions. Advancing age consequences in cut down stomachic acid secernment, stomachic voidance, GI mobility, surface country for soaking up, liver size and map, nephritic map, thin organic structure mass, entire H2O content, serum albumen, cardiac end product and increase organic structure fat which affect straight or indirectly drug metamorphosis and can take to toxicity. Drug METABOLISMS Metamorphosis is a procedure that cause drugs to go more H2O soluble in order to readily take them from the organic structure after they have perform their action in the organic structure. This procedure takes topographic point chiefly in the liver cells and produces metabolites which are non active and sometimes non-toxic, although some metabolites may be toxic. There are drugs that their parent drug are in active and the metabolites produced are active. The mechanisms of drug metamorphosiss are divided into stage I and phase II. Phase I reactions involves structural alteration of drug molecules and stage II reaction dwelling of junction with a more H2O soluble compound. Oxidation, decrease and hydrolysis are chief reaction happening in stage I with engagement of cytochrome p450 enzymes an other enzymes are besides involved in oxidative metamorphosis ( Strolin Benedetti, M. et Al ) . Maturational alterations occurs from birth in both stage I and phase II metabolic tracts which is no rmally non to the full mature at birth. The liver is most of import organ for drug metamorphosis quantitatively and signifiers about 6 % of the organic structure mass at birth but around 3 % of the organic structure mass in the grownup. Growth is associated with decrease in blood fluxing into the liver and liver volume accordingly ensuing in reduced metabolic clearance with drugs that require high hepatic remotion whereas drugs with low hepatic remotion are normally less removed which can take to toxicity. Depending on the enzyme system involved, there can be production of low or high plasma concentration of active rule due to different capacities to metabolise drug in the paediatric or older people than in grownup. There are healing agent in kids that produces metabolites whereas this metabolites are non present usually in grownup and the metabolites may be the cause of efficaciousness and/or toxicity seen with disposal of drug in kids for illustration kids having Elixophyllin produces caffeine ( Olive et Al. ) and other illustrations of healing agent that differ in metabolite production are paracetamol, salicylamide, Chloromycetin, valproic acid and Tagamet. There is besides different in degree of look of metabolites in kids compared to adult although they express the same enzyme complement but there is no cognition of illustration of metabolite production non usually present in grownup that are seen in the older population. Few exclusions occurs though in most instances because differences between the kids and grownups are in ratio of metabolite compared to the parent drug instead than metabolites that are unevenly specific to the paediatric. PHASE IREACTIONS OXIDATIVE ENZYMES CYTOCHROME P450 ( CYP ) SYSTEM The oxidative metamorphosis of many drugs and chemicals are catalyze by cytochrome p450 isoenzyme superfamily that consist of over 50 proteins. The enzymes are present in the smooth endoplasmic Reticulum of the liver and other tissue in their lipotropic membrane which can be isolated and they become cysts called microsomes. Different cytochrome p450 household are responsible for different metamorphosis for illustration cytochrome p450 households 1-4 are responsible for foreign compounds metamorphosis while the other cytochrome p450 households are responsible for endogenous substrates metamorphosis. The metabolic activation of many chemical carcinogens and toxins that undergoes metamorphosis and used clinically are besides the duty of cytochrome p450. CYP1A There are two isoforms of CYP1A subfamily viz. CYP1A1 AND CPY1A2. CYP1A1 are chiefly extra-hepatic. CYP1A2 is concerned chiefly with the metamorphosis of paracetamol, caffeine, Elixophyllin, impramine hydrochloride, aromatic aminoalkanes, Coumadin and acetophenetidin. All demethylations of N-1, N-3, N-7 and pealing hydroxylation of C-8 in the metamorphosis of caffeine and Elixophyllin are besides the duty of CYP1A2 and other CYP isozymes like CYP3A4/5, CYP2A6 and CYP2E1 besides take portion in these reaction ( Oesterheld et al, Kalow, W. and Tang et al. ) . In pediatric, CYP1A2 is non normally noticeable until one to three months infant age and its additions until about three old ages but remains the same with big degree afterwards. Demethylation of caffeine N-3 depends on CYP1A2 in newborns, babies and grownups but N-3 demethylation is more of import in immature babies. Caffeine metabolic tract matures with postpartum age particularly with entire demethylation, demethylation of N-7 and N-3 demethylation whereas demethylation of N-1 show no fluctuation but ripening occurs at one and half old ages of age. Hydroxylation of C-8 is normally developed at one month in few babies than in grownups. The activity of most demethylation was found to be lower in newborns and babies than grownup and diet of babies besides affect development of CYP1A2 activity ( Blake, M.J. et Al ) . There is lessening in activity of CYP1A2 in aged with caffeine. Most of this fluctuation leads to toxicity and it s dose dependent excessively. CYP2A There are three isoforms of this subfamily viz. CYP2A6, 2A7 and 2A13 ( Hakkola, J. et Al ) . CYP2A6 is chiefly involved in contact action of coumarin 7-hydroxylation ( Pelkonen, O. et Al ) . Urinary elimination of 7-hydroxycoumarin is about the same in kids of six to fourteen old ages and grownups but the rate of riddance is unchanged or reduced for CYP2A substrates in the aged which can do toxicity in relation to dose given. CYP2A6 is non seen in fetal liver. CYP2C The isoforms of this subfamily are CYP2C9, CYP2C19 and CYP2C8. They are involved in metamorphosis of assorted curative agent for illustration anti-inflammatory drugs ( non-steroidal ) , antiepileptics, Coumadin, propranolol, Valium etc and might lend to metamorphosis of endogenous agents e.g arachidonic acid. CYP2C isozymes is noticeable early in neonatal period, one month degree is normally about tierce of grownups and remains the same until about one twelvemonth of age. From birth there is interindividual fluctuation in CYP2C9 protein and activity until about 18years with 36 crease boulder clay five months and less fluctuation between five months and 18 old ages. Phenytoin ( antiepileptic ) and substrate of CYP2C9 pharmacokinetics is affected which can take to toxicity. Expression of CYP2C19 additions from birth for approximately five month and fluctuation of single between five months and ten old ages is about 22 creases but from ten old ages at that place is similarity in activit y and look with grownup ( Blanco, J.G. et Al ) . In the aged there is lessening in the rate of riddance of substrates of both CYP2C19 and CYP2C9 ( Kinirons, M.T. et al and Cusack et Al. ) likely doing toxicity depending on dosage. CYP2D CYP2D6 is involved in the metamorphosis of drugs like A ; szlig ; -blockers, anti jerking drugs, antidepressants ( tricyclic and non-tricyclic ) , codeine, Capoten, ondansetron etc ( Strolin Benedetti, M. et Al ) . There is addition in the protein look of CYP2D6 from few hebdomads postpartum age to about five old ages and reaches about two- tierce of the grownup degree. There is besides CYP2D6 polymorphism in kids but there is unchanged rate of riddance of substrates of CYP2D6 in the aged. Most of this change with age can impact the metamorphosis taking to toxicity and it s dose dependant. CYP2E CYP2E1 contribute to the metamorphosis of little molecules like paracetamol, aminobenzine, ethyl alcohol, N-nitrosodimethylamine ( strolin Benedetti, M. et Al ) . The enzymes rises after birth boulder clay about one twelvemonth and go approximately 40 % of big degree but reaches 100 % grownup degree between one twelvemonth and 10 twelvemonth ( strolin Benedetti, M. et Al ) . It decrease or stay unchanged with age utilizing substrates like paracetamol and chloroxazone ( Kinirons et Al and OMahony et Al. ) but recent survey shows that there is addition in CYP2E1 activity with age in work forces than in adult females ensuing in toxicity depending on dosage. CYP3A CYP3A isoforms are CYP3A4, CYP3A5, CYP3A7 ; they are the major CYP isoforms found in the liver and little bowel. They are besides involved in oxidization of legion substrates.CYP3A5 is independent of age and variably high in look ( Steven et al. ) . CYP3A4 is majorly expressed in grownup liver while CYP3A7 is majorly expressed in fetal liver. The isoforms are closely related structurally but differs in monooxygenase reaction capacity map. CYP3A7 in fetal liver is really active until after first hebdomad of birth and starts to diminish till it is absent in grownup liver. CYP3A4 is really weak or non present in fetus but rises after birth and it is responsible for biotransformation of cisapride ( serotonin 5-HT4 agonist ) which can do cardiac toxicity in newborns due to steady addition in activity of CYP3A4 in metamorphosis of cisapride that exceeds grownups value activity particularly in newborns and grownup that do nt transport hazard factor impacting them. Another CYP3A4 substrate, endovenous Versed ( ataractic ) metamorphosis is lower in newborns than in babies greater than 3months of age but as a consequence of low activity of CYP3A4 in the bowel of grownup there is addition in bioavailability of Versed following unwritten consumption in preterm babies compared to grownups ( De Wildt, S.N. et Al ) . CYP3A4 development is fastened with diet in babies ( Blake, M.J. et Al ) . In the aged there is inconclusive information about the activity and look of CYP3A but it remain unchanged or lessening with age ( Schmucker et al. ) . FLAVIN-CONTAINING MONOOXYGENASES ( FMOs ) Flavin- containing monooxygenases are critical in oxidative of assorted foreign compounds incorporating nucleophilic N, phosphorus-heteroatoms, Se, S that are NADPH dependant. There are six member cistron household of the enzyme ( FMO 1-6 ) . In the paediatric, FMO1 look was highest from 2months to 4months gestation and a mechanism coupled with construct suppressed wholly look of FMO1 within three yearss post natal. FMO3 look was non present during neonatal period but low degree was present between 2months and 4months gestation ; from one to two old ages of age FMO3 look was present and increase boulder clay about 11 old ages but from 11 old ages to eighteen old ages, there is gender -interdependence in the addition of FMO3 look ( Strolin Benedetti, M. et Al ) . There is a hepatic nothing FMO phenotype in newborn due speedy station natal suppression of FMO1 and FMO3 look delayed oncoming. MONOAMINE OXIDASES ( MAOs ) Monoamine oxidases are involved in the exogenic and endogenous compounds metamorphosis and found in the chondriosome of liver, kidney, lungs, encephalon, bowel and thrombocytes ( Strolin Benedetti, M. et al. ) . Their concentration is low in liver and higher in other tissues. The two monoamine oxidases that take portion in drug metamorphosis are MAO A and MAO B. During construct MAO A activity is really high and reduces rapidly in the first two twelvemonth of age and becomes steady afterwards. MAO B activity is low at construct, steady in early age and increases with progressing age. ALCOHOL DEHYDROGENASE ( ADH ) Alcohol dehydrogenases are cytosolic isozymes that are involved in the reversible oxidization of intoxicants to aldehydes and metamorphosis of endogenous compounds like steroids and vitamin A1. For illustration Atarax to cetirizine. There are six categories of intoxicant dehydrogenase ADH 1-6, five of the ADH 1-5 are found in adult male ( Strolin Benedetti, M. et al. ) . In newborns, there is immature development of the activity of ADH but from one to two and half twelvemonth of age, the activity of ADH is the same or greater than in grownup. There is no much difference in the activity of ADH in grownup compared to the aged. MOLYBDENUM HYDROXYLASES ( ALDEHYDE OXIDASE AND XANTHINE OXIDASE ) Aldehyde oxidase ( AO ) and Xanthine oxidase ( XO ) are involved in exogenic and endogenous substrates biotransformation. XO is involved in oxidative hydroxylation of hypoxanthine to xanthine, xanthine to uric acid and purine metamorphosis last two stairss in mammals. AO and XO are similar structurally but AO takes portion in metamorphosis of estrogen antagonist, ziprasidone, zaleplon, famciclovir, zonisamide etc. XO activity in plasma is really high in babes compared to adult and AO activity is immature until about 12months after ( Karg, E. et Al and Tayama, Y. et Al ) . XO activity is independent of age in aged. REDUCTIVE ENZYMES NADPH-CYTOCHROME P450 REDUCTASE The negatron giving spouse to CYP enzymes are flavin adenine dinucleotide ( FAD ) and flavin mononucleotide ( FMN ) contained in the cytochrome p450 reductase. NADPH cut downing enzymes are passed to the FAD of cytochrome p450 reductase and so to CYP enzymes via the FMN of the cytochrome p450 reductase. There is no much important alteration with age with NADPH-cytochrome p450 reductase ( Schmucker et al. ) . ALDO-KETOREDUCTASES Aldo ketoreductases are present in red blood cells, liver and are cytosolic enzymes involved in decrease of carbonyl groups. They besides metabolized hypolipidemic drugs ( fenofibrate ) and anti malignant neoplastic disease drugs ( anthracyclines ) . Prostaglandin E1 ( PGE1 ) are metabolized by ketoreductase. ketogroup decrease frequently produce active metamorphosis which can do toxicity with age for illustration idarubicin produces idarubicinol ( alcohol merchandise ) and PGE1 produces 13,14-dihydro-15- ketoprostaglandin E1 which is farther cut down to active compound 13, 14-dihydro-prostaglandin E1. HYDROLYTIC ENZYMES ESTERASES There is lessening in the activity of esterases in newborn than in grownup but in the aged physical failing reduces the activity of esterases particularly those with injuries, undergoing surgery, injured or ill. From 7months gestation to 12months of age, there is speedy addition in the activity of plasma arylesterase and pseudocholinesterase activity, but no important change occurs afterwards. There is disconnected addition in erythrocyte acetylcholinesterase activity between construct and 12months i.e red blood cells are non matured before construct. Ester signifiers of drugs are largely incompletely hydrolyzed in newborns due to low serum concentration that consequence e.g Erythrocin estolate, Chloromycetin palmitate ( Morselli, P.L. et al. ) . PHASE II REACTIONS Acetylation Junction with acetyl group by drugs like INH, p-aminosalicylic, p-aminobenzoic acid, sulfamezathine and toxic agent is control by activity of N-acetyltransferase ( NAT ) . in premature and neonates, there is acetylation of p-aminobenzoic acid by N-acetyltransferase1 ( NAT1 ) which increase somewhat in babies and is reduced in kids ( Strolin Benedetti, M. et al. ) . N-acetyltransferase2 ( NAT2 ) involved in caffeine and INH metamorphosis shows that in babies there are slow acetylators or fast acetylators that are non matured with caffeine and with isoniazid acetylation ripening occurs after one twelvemonth, as fast acetylors increases with age till four old ages peak. METHYLATION Junction of methyl group are the duty of S-methytransferase, O-methyltransferase, and N-methyltransferase which are involved in transportation of methyl group to oxygen-nucleophile, nitrogen-nucleophile and sulfur nucleophile. N-methyltransferases Theophylline N-7-methylation in newborn to caffeine is good matured but oxidative demethylation is deficient and matures after several months of age. Thiopurine-s-methyltransferase Thiopurine-s-methyltransferase ( TPMT ) is involved in the metamorphosis of azathiopurine ( converted to 6-MP ) and catalyzes thiopurines metamorphosis e.g 6-MP ( antiblastic drug ) . TPMT is a cytosolic polymorphic enzyme which is cistron specific and are present in many tissue and red blood cell. In pediatric, there is high activity of TPMT in approximately 90 % of the population, approximately 8 % have intermediate activity and 0.3 % have low activity. Inactivation by TPMT which affects the efficaciousness of 6MP in single with low TPMT activity experience terrible toxicity with 6MP standard doses. GLUCURONIDATION There are assorted UDP glucoronsyltransferase ( UGT ) isozymes present in human. Glucuronidation in pediatric ranges adult degree when they are 12weeks to24weeks old, 12months, 36months or subsequently in age depending on the drug. At 12weeks of age, hematoidin glucuronidation which is the duty of UGT1A1 isozymes approach big degree but occurs at really low degrees in newborns liver. For illustration Chloromycetin with lower glucuronidation in paediatric can take to toxicity because glucuronidation is clearly deficient in most premature babes and mature babes. Therefore high concentration of unmetabolized Chloromycetin may increase in sum taking to serious toxicity which cause go arounding prostration or gray baby syndrome with standard dosage per bodyweight. These prompt the more surveies and the dosage was regulated on weight, gestation and postpartum age footing. UGT2B7 besides metabolize Chloromycetin and some UGT isoforms besides eliminates it. 3-glucuronides ( M3G ) and 6-glucu ronides ( M6G ) are formed as a consequence of UGT2B7 metabolising morphia. There is addition in the quality of morphine glucuronidation activity after neonate age. For illustration there is addition in epirubicin glucuronidation activity with age and riddance of epirubicin ( malignant disease intervention ) is majorly by UGT2B7 glucuronidation. In kids of 7 to 10 twelvemonth, there is deficient glucuronidation of paracetamol and salicylamide in correlativity with grownups ( Alam, S.M. et al. ) . UGT1A6 is the chief glucuronidation isozymes of paracetamol although UGT1A1 and UGT1A9 besides takes portion in the glucuronidation ( Court, M.H. et al. ) . Strassburg et Al. observed that UGT1A1, 1A3, 2B15, 2B4, 1A4, 2B7, 1A6, 2B10 and 1A9 are present after 6 months of age. There is different in look of UGT1A1, 1A6 and 2B6 protein but lower messenger RNA look for UGT2B4, 1A9 was seen. Hepatic glucuronidation activity in 1-2years is low compared to grownups for the undermentioned drugs e.g buprenorphine, Elavil, isobutylphenyl propionic acid, theelin, 4-tert-butylphenol. Acyl co-enzymes A, phospholipid content, fatty acid with long concatenation and membrane factors may be responsible for enzymatic activities differences between pediatric and grownup. In aged, there is decreased glucuronidation of lamotrigine and riddance of Serax, retigabine by UGT activity. SULFATION The sulfate junction of several endogenous and exogenic chemicals by sulfotransferase ( SULT ) cistron household that encodes about 11 major enzymes utilizing 3-phosphoadenosine-5-phosphosulfate ( PAPS ) . In peadiatric, there is ripening of sulfate tract at construct which is the chief metabolic path in baby and kids for salicylamide and paracetamol ( Alam, S.M. et al. ) . For illustration in morphine metamorphosis sulfate junction can counterbalance for the less-matured glucuronidation. Junction WITH AMINO ACIDS Biotransformation of some compounds is dependent on the junction of foreign compounds of carboxylic acids with endogenous amino acids. In worlds glycine, glutamine and taurine are aminic acids that undergoes junction often. In pediatric, junction with glycine additions from construct to kids age and is the major tract for metamorphosis of salicylates in newborns ( strolin Benedetti, M.et al. ) . Formation of hippuric acid by glycine junction of benzoic acid is present but deficient in preterm babes. Junction WITH GLUTATHIONE Cytosolic glutathione S-transferase ( GST ) is responsible for junction of glutathione. Catalysiss of conjugate of different electrophiles with decreased glutathione is the major manner by which GSTs metabolize carcinogens, exogenic and endogenous toxins. In pediatric within 12-24months, there is addition in GSTA1 and GSTA2 look to adult degree with norm of 3 crease and GSTM look increased to about 5 crease to adult degree at construct. In grownup liver there is no GSTP1 but it is present in newborns. GST activity and GSTP1 degree in female merely showed of import addition from less than 50 old ages to over 70 old ages ( Hoensch, H. et al. ) . Decision The increasing fluctuation between single in enzymes activity involved in drug metamorphosis coupled with other physiological factors make it hard to distinguish age effects on drug metamorphosis in relation to toxicity but a good cognition about the drugs pharmacokinetics is really of import to cognize patient population that requires dosage accommodation in order to forestall toxicity ( acute or chronic ) after exposure. A better apprehension of the specific drug metabolising enzymes with age fluctuation is besides critical in ordering drugs to patient population and in development of drugs in the patient population. Most drugs metabolized through the cytochrome p450 enzymes decreases with age every bit good as the nephritic riddance of most drugs decreases with age which can take to toxicity. Mentions Strolin Benedetti, M et Al. ( 2005 ) Differences in soaking up, distribution, metamorphosis and elimination between the paediatric and the grownup population. Expert Opin. Drug Metab. Toxicol. 1, 447-471 Cazeneuve, C. et Al. ( 1994 ) Biotransformation of caffeine in human liver microsomes from foetuss, newborns, babies and grownups. Br. J. Clin. Pharmacol. 37, 405-412. Zeeh, J. et Al ( 1996 ) Influence of age, infirmity and liver map on the pharmacokinetics of brofaromine. Eur. J. Clin. Pharmacol. 49, 387-391 Simon, T. ( 2001 ) Variability of cytochrome P450 1A2 activity over clip in immature and aged healthy voluntaries. Br. J. Clin. Pharmacol. 52, 601-604 Kinirons, M.T. and OMahony, M.S. ( 2004 ) Drug metamorphosis and ageing. Br. J. Clin. Pharmacol. 57, 540-544 Cusack, B.J. ( 2004 ) Pharmacokinetics in older individuals. Am. J. Geriatr. Pharmacother. 2, 274-302 Koukouritaki, S.B et Al. ( 2004 ) Development look of human hepatic CYP2C9 and CYP2C19. J. pharmacol. Exp. Ther. 308, 965-974 Blanco, J.G. et Al. ( 2000 ) Human cytochrome P450 maximum activities in paediatric versus grownup liver. Drug Metab. Dispos. 28, 379-382 George, J. et Al. ( 1995 ) Age but non gender selectively affects look of single cytochrome P450 proteins in human liver. Biochem. Pharmacol. 50,727-730 Schmucker, D.L. ( 2001 ) Liver map and Phase I drug metabolim in th aged. A paradox. Drugs Aging 18, 837-851 Ishizawa, Y. et Al. ( 2005 ) The consequence of aging on the relationship between the cytochrome P450 2C19 genotype and omeprazole pharmacokinetics. Clin. Pharmacokinet. 44, 1179-1189 Foglia, J.P et Al. ( 1997 ) Plasma degrees of citalopram enantiomorphs and metabolites in aged patients. Psychopharmacol. Bull. 33, 109-112 Stevens, J.C. ( 2006 ) New positions on the impacts of cytochrome P450 3A look for paediatric pharmacological medicine. Drug Discov. Today 11, 440-445 De Wildt, S.N. et Al. ( 2002 ) Pharmacokinetics and metamorphosis of unwritten Versed in preterm babies. Br. J. clin. Pharmacol. 53, 390-392 Patki, K.C. ( 2004 ) Consequence of age on in vitro triazolam biotransformation in male human liver microsomes. J. pharmocol. Exp. Ther. 308, 874-879 Strolin Benedetti, M. et Al. ( 1992 ) Developmental facets of the monoamine-degrading enzymes monoamine oxidases. Dev. Pharmacol. Ther. 18, 191-200 Kornhuber, J. et Al. ( 1989 ) Growth of monoamine oxidase-A and -B in the human encephalon frontal cerebral mantle. Brain Res. 499, 81 Karg, E.et Al. ( 2001 ) Ferroxidases and xanthine oxidoreductase in plasma of healthy newborn babies. Free Radic. Res. 35, 555-561 Tayama, Y. et Al. ( 2007 ) Developmental alterations of aldehyde oxidase activity in immature Nipponese kids. Clin. Pharmacol. Ther. 81, 567-572 Eskura, I. et Al. ( 2006 ) Xanthine oxidase does non lend to impaired peripheral conduit arteria endothelium-dependent distension with ageing. J. Physiol. 571, 661-668 Ecobichon, D.J. and Stephens, D.S. ( 1971 ) Perinatal development of blood exterases. Clin. Pharmacol. Ther. 14, 41-47 Morselli, P.L. et Al. ( 1980 ) Clinical pharmacokinetics in neonates and babies. Clin. Pharmacokin. 5, 485-527 Puche, E. et Al. ( 1989 ) Serum aspirin-esterase activity in epileptic patients having intervention with Phenobarbital, diphenylhydantoin, carbamazepine and valproic acid. Int. J. Clin. Pharm. Res. IX, 55-58 Pope, C.N. et Al. ( 2005 ) Comparative carboxylesterase activities in babies and grownup liver and their in vitro sensitiveness to chlorpyrifos oxon.Regul. Toxicol. Pharmacol. 42, 64-69 Abou Hatab, K. et Al. ( 2001 ) Relationship between age and plasma esterases. Age Aging 30, 41-45 Alam, S.M. et Al. 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Celebrity SAT Scores (Kesha, Bill Gates, and more)

Celebrity SAT Scores (Kesha, Bill Gates, and more) SAT / ACT Prep Online Guides and Tips What do you have in common with Kesha, Bill Gates, Al Gore, and Derek Jeter? They all had to take the SAT when they were in high school, just like you! However you feel about the SAT, it’s a landmark in the lives of many American students (and lots of international ones, too). Taking the SAT is an experience that many of you will share and remember well for the rest of your lives. Let’s check out some SAT scores of the rich and famous - and talk about how you can achieve some Kesha-worthy scores of your own. Feature image: Nicole Abalde/Flickr SAT Scores of Famous People We've gathered a complete list of celebrity SAT scores. These were often revealed in interviews or through investigative research. Some people were proud of their high scores, others proud of their low scores - and others couldn't care less. Here it is: Celebrity SAT Score (out of 1600) College Attended Paul Allen 1600 Washington State University Will Smith Rumored to be perfect None Ben Affleck Almost perfect Occidental College, University of Vermont Bill Gates 1590 Harvard Ben Bernanke 1590 Harvard Bill O'Reilly 1585 Marist College Ryan Fitzpatrick 1580 Harvard James Woods 1579 MIT Ben Stein 1573 Columbia Kesha 1500 None Scott McNealy 1420 Stanford Natalie Portman 1400+ Harvard Al Gore 1355 Harvard Stephen King 1300s University of Maine Meredith Vieira 1300s Tufts University George W. Bush 1206 Yale Derek Jeter 1200 University of Michigan John Kerry 90 Yale Courtney Cox 50 Mount Vernon College Amy Tan 00s Linfield College, San Josà © State University Kobe Bryant 1080 None Scarlett Johansson 1080 None Bill Clinton 1032 Georgetown Peyton Manning 1030 University of Tennessee Alex Rodriguez 910 None Clearly all people on this list are considered successful, indicating you don't need a high SAT score to be successful, if you have passion, drive, and talent. You can either get a Kesha-like SATscore of 1500 or a Kobe-like one of 1080. But for most people in the world (like you and me), working hard in school, getting good grades, and earning high scores set up a brighter future with more open opportunities. Actors, singers, athletes, entrepreneurs, and politicians are scattered all up and down the list, but how can you join the ranks of Bill Gates, Will Smith, and Kesha up at the top? Read on for the important strategies and resources you need to score high on the SAT. Walmart/Flickr Where Will You Fall On This List? You need a high SAT score to get into good colleges, and we've got tips for you to improve your score. Get to Know the SAT Well To do well on the SAT, you have to know the SAT - you must be familiar with its content and format, as well as able to work fast and efficiently. High quality materials are a must in readying yourself and improving your scores. Questions that aren’t well written or don’t match the complexity of real SAT questions won’t get you very far. Timing yourself as your practice will also help you with pacing. Study Smart, Not Dumb Getting ready is not just about how much you prep, but about how well you prep. There are several important strategies to your approach, including setting small, manageable goals and rooting out your particular strengths and weaknesses. Check out our free E-Book for the tips you need to know to customize your study methods to your abilities and learning style. Understand the Test Inside and Out By the time you take the SAT, you don’t want to have any lingering questions or uncertainties about the test, including how long the sections are or how your scores are calculated. To learn the ins and outs of the SAT, check out our numerous resources. Just a few good places to start involve how long the test is, how it is scored, and how you can get a perfect SAT score. Know About Upcoming SAT Changes These celebs took the old version of the SAT, when it was scored out of 1600. The current SAT is scored out of 2400, with a maximum possible score of 800 for Critical Reading, Math, and Writing. Starting in the spring of 2016, however, the redesigned SAT will return to the 1600 scale system, with a maximum point value of 800 for Critical Reading and Writing (together) and 800 for math. There are several other changes in content that you should know about if you’ll be taking the new SAT. The new PSAT, furthermore, which all juniors will take in the fall, is changing this year (2015) to match the new SAT. Read about the redesign here, and learn how it will help next year’s juniors prepare for the new SAT. The SAT is a rite of passage that many high school students share on the road to college. What scores will end up being reported for you? What’s Next? No two people are exactly the same, so no two approaches to studying should be the same either. A good starting point to customizing your SAT prep to your unique strengths and skills is setting personalized goals. Find out what’s a good SAT score, a bad SAT score, and an excellent SAT score here so you can set your own individual target scores. The SAT is a long and important test, so obviously you wouldn’t be well served by only cramming the night before. But when exactly should you start prepping for the SAT? Learn how to schedule out your time to effectively study for the SAT. Want to improve your SAT score by 160 points? Check out our best-in-class online SAT prep program. We guarantee your money back if you don't improve your SAT score by 160 points or more. Our program is entirely online, and it customizes your prep program to your strengths and weaknesses. We also feature thousands of practice questions, 10 official SAT practice tests, and personal feedback on your essays from an expert instructor. Check out our 5-day free trial: