Overview of the short-term effects of the consumption of alcoholic beverages
The short-term effects of alcohol consumption range from a decrease in anxiety and motor skills and euphoria at lower doses to intoxication (drunkenness), to stupor, unconsciousness, anterograde amnesia (memory "blackouts"), and central nervous system depression at higher doses. Cell membranes are highly permeable to alcohol, so once it is in the bloodstream, it can diffuse into nearly every cell in the body.
The concentration of alcohol in blood is measured via blood alcohol content (BAC). The amount and circumstances of consumption play a large role in determining the extent of intoxication; for example, eating a heavy meal before alcohol consumption causes alcohol to absorb more slowly.[1] The amount of alcohol consumed largely determines the extent of hangovers, although hydration also plays a role. After excessive drinking, stupor and unconsciousness can both occur. Extreme levels of consumption can cause alcohol poisoning and death; a concentration in the blood stream of 0.36% will kill half of those affected.[2][3][4] Alcohol may also cause death indirectly by asphyxiation, caused from vomiting.
Alcohol can greatly exacerbate sleep problems. During abstinence, residual disruptions in sleep regularity and sleep patterns[clarification needed] are the greatest predictors of relapse.[5]
Effects by dosage
The definition of a unit of alcohol ranges between 8 and 14 grams of pure ethanol depending on the country.[6] There is no agreement on definitions of a low, moderate or high dose of alcohol either. The U.S. National Institute on Alcohol Abuse and Alcoholism defines a moderate dose as alcohol intake up to two standard drinks or 28 grams for men and one standard drink or 14 grams for women.[7] The immediate effect of alcohol depends on the drinker's blood alcohol concentration (BAC). BAC can be different for each person depending on their age, sex, pre-existing health condition, even if they drink the same amount of alcohol.[8]
Different BACs have different effects. The following lists describe the common effects of alcohol on the body depending on the BAC. However, tolerance varies considerably between individuals, as does individual response to a given dosage; the effects of alcohol differ widely between people. Hence in this context, BAC percentages are just estimates used for illustrative purposes.
Research shows an exponential increase of the relative risk for a crash with a linear increase of BAC.[10] NHTSA reports that the following blood alcohol levels (BAC) in a driver will have the following predictable effects on his or her ability to drive safely: (1) A BAC of .02 will result in a "[d]ecline in visual functions (rapid tracking of a moving target), a decline in the ability to perform two tasks at the same time (divided attention)"; (2) A BAC of .05 will result in "[r]educed coordination, reduced ability to track moving objects, difficulty steering, reduced response to emergency driving situations"; (3) A BAC of .08 will result in "[c]oncentration, short-term memory loss, speed control, reduced information processing capability (e.g., signal detection, visual search), impaired perception"; (4) A BAC of .10 will result in "[r]educed ability to maintain lane position and brake appropriately"; and (5) A BAC of .15 will result in "[s]ubstantial impairment in vehicle control, attention to driving task, and in necessary visual and auditory information processing."[11]
Moderate doses
Ethanol inhibits the ability of glutamate to open the cation channel associated with the N-methyl-D-aspartate (NMDA) subtype of glutamate receptors. Stimulated areas include the cortex, hippocampus, and nucleus accumbens, which are all responsible for both thinking and pleasure seeking. Another one of alcohol's agreeable effects is body relaxation, which is possibly caused by neurons transmitting electrical signals in an alpha waves-pattern; such waves are actually observed (with the aid of EEGs) whenever the body is relaxed.[citation needed]
Short-term effects of alcohol include the risk of injuries, violence, and fetal damage.[12] Alcohol has also been linked with lowered inhibitions, although it is unclear as to what degree this is chemical or psychological as studies with placebos can often duplicate the social effects of alcohol at either low or moderate doses. Some studies have suggested that intoxicated people have much greater control over their behavior than is generally recognized, though they have a reduced ability to evaluate the consequences of their behavior.[13] Behavioral changes associated with drunkenness are, to some degree, contextual.[14][15]
Areas of the brain that are responsible for planning and motor learning are sharpened. A related effect, which is caused by even low levels of alcohol, is the tendency for people to become more animated in speech and movement. This is caused by increased metabolism in areas of the brain associated with movement, such as the nigrostriatal pathway. This causes reward systems in the brain to become more active, which may induce certain individuals to behave in an uncharacteristically loud and cheerful manner.
Alcohol has been known to mitigate the production of antidiuretic hormone, which is a hormone that acts on the kidney to favor water reabsorption in the kidneys during filtration. This occurs because alcohol confuses osmoreceptors in the hypothalamus, which relay osmotic pressure information to the posterior pituitary, the site of antidiuretic hormone release. Alcohol causes the osmoreceptors to signal that there is low osmotic pressure in the blood, which triggers an inhibition of the antidiuretic hormone. As a consequence, one's kidneys are no longer able to reabsorb as much water as they should be absorbing, therefore creating excessive volumes of urine and the subsequent overall dehydration.[citation needed]
Acute alcohol intoxication through excessive doses in general causes short- or long-term health effects. NMDA receptors become unresponsive, slowing areas of the brain for which they are responsible. Contributing to this effect is the activity that alcohol induces in the gamma-aminobutyric acid (GABA) system. The GABA system is known to inhibit activity in the brain. GABA could also be responsible for causing the memory impairment that many people experience. It has been asserted that GABA signals interfere with both the registration and the consolidation stages of memory formation. As the GABA system is found in the hippocampus (among other areas in the CNS), which is thought to play a large role in memory formation, this is thought to be possible.
Anterograde amnesia, colloquially referred to as "blacking out", is another symptom of heavy drinking.[16] This is the loss of memory during and after an episode of drinking.
Another classic finding of alcohol intoxication is ataxia, in its appendicular, gait, and truncal forms. Appendicular ataxia results in jerky, uncoordinated movements of the limbs, as if each muscle were working independently from the others. Truncal ataxia results in postural instability; gait instability is manifested as a disorderly, wide-based gait with inconsistent foot positioning. Ataxia causes the observation that drunk people are clumsy, sway back and forth, and often fall down. It is presumed to be due to alcohol's effect on the cerebellum.[17]
Mellanby effect
The Mellanby effect is the phenomenon that the behavioral impairment due to alcohol is less, at the same BAC, when the BAC is decreasing than when it is increasing.[18] This effect was confirmed in a 2017 meta-analysis.[19]
Effect on different population
Based on sex
Alcohol affects males and females differently because of difference in body fat percentage and water content. On average, for equal body weight, women have a higher body fat percentage than men. Since alcohol is absorbed into body water content and men have more water in their bodies than women, for women there will be a higher blood alcohol concentration from the same amount of alcohol consumption.[20] Women are also thought to have less alcohol dehydrogenase (ADH) enzyme which is required to break down alcohol.[8] That is why the drinking guidelines are different for men and women.[21]
Based on genetic variation
Alcohol metabolism depends on the enzymes alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH).[22] Genetic variants of the genes coding for these enzymes can affect the rate of alcohol metabolism. Some ADH gene variants lead to higher metabolic activity, resulting in the accumulation of acetaldehyde, whereas, a null allele in ALDH2 causes an accumulation of acetaldehyde by preventing its catabolism to acetate.[23] The genetic variants of these enzymes can explain the differences in the alcohol metabolism in different races. The different isoforms of ADH showed protection against alcoholic disorders in Han Chinese and Japanese (due to presence of ADH1B*2 ) and in African (due to presence of ADH1B*3).[24] On the other hand, presence of ALDH2*2 in East Asians (a variant of the ALDH gene), can cause blood acetaldehyde levels of 30 to 75 μM or higher, which is more than 10 times the normal level. The excess amount of blood aldehyde produce facial flushing, nausea, rapid heartbeat, and other adverse effects.[25][26] Presence of these alleles causes rapid conversion of alcohol to acetaldehyde which can be toxic in large amount. So, the East Asians and Africans feel the adverse effects of alcohol early and stop drinking. For Caucasians, ADH1B*1 allele is the most prevalent allele which causes slower conversion of alcohol to acetaldehyde and it makes them more vulnerable to alcohol use disorders.[27]
Humans metabolize ethanol primarily through NAD+-dependent alcohol dehydrogenase (ADH) class I enzymes (i.e. ADH1A, ADH1B, and ADH1C) to acetaldehyde and then metabolize acetaldehyde primarily by NAD2-dependent aldehyde dehydrogenase 2 (ALDH2) to acetic acid.[28][29] Eastern Asians reportedly have a deficiency in acetaldehyde metabolism in a surprisingly high percentage (approaching 50%) of their populations. The issue has been most thoroughly investigated in native Japanese where persons with a single-nucleotide polymorphism (SNP) variant allele of the ALDH2 gene were found; the variant allele, encodes lysine (lys) instead of glutamic acid (glu) at amino acid 487; this renders the enzyme essentially inactive in metabolizing acetaldehyde to acetic acid.[30][31] The variant allele is variously termed glu487lys, ALDH2*2, and ALDH2*504lys. In the overall Japanese population, about 57% of individuals are homozygous for the normal allele (sometimes termed ALDH2*1), 40% are heterozygous for glu487lys, and 3% are homozygous for glu487lys.[31] Since ALDH2 assembles and functions as a tetramer and since ALDH2 tetramers containing one or more glu487lys proteins are also essentially inactive (i.e. the variant allele behaves as a dominant negative), homozygote individuals for glu487lys have undetectable while heterozygote individuals for glu487lys have little ALDH2 activity.[32] In consequence, Japanese individuals homozygous or, to only a slightly lesser extent, heterozygous for glu487lys metabolize ethanol to acetaldehyde normally but metabolize acetaldehyde poorly and are susceptible to a set of adverse responses to the ingestion of, and sometimes even the fumes from, ethanol and ethanol-containing beverages; these responses include the transient accumulation of acetaldehyde in blood and tissues; facial flushing (i.e. the "oriental flushing syndrome" or Alcohol flush reaction), urticaria, systemic dermatitis, and alcohol-induced respiratory reactions (i.e. rhinitis and, primarily in patients with a history of asthma, mild to moderately bronchoconstriction exacerbations of their asthmatic disease.[33] These allergic reaction-like symptoms, which typically occur within 30–60 minutes of ingesting alcoholic beverages, do not appear to reflect the operation of classical IgE- or T cell-related allergen-induced reactions but rather are due, at least in large part, to the action of acetaldehyde in stimulating tissues to release histamine, the probable evoker of these symptoms.[33][34]
The percentages of glu487lys heterozygous plus homozygous genotypes are about 35% in native Caboclo of Brazil, 30% in Chinese, 28% in Koreans, 11% in Thai people, 7% in Malaysians, 3% in natives of India, 3% in Hungarians, and 1% in Filipinos; percentages are essentially 0 in individuals of Native African descent, Caucasians of Western European descent, Turks, Australian Aborigines, Australians of Western European descent, Swedish Lapps, and Alaskan Eskimos.[34][35] The prevalence of ethanol-induced allergic symptoms in 0 or low levels of glu487lys genotypes commonly ranges above 5%. These "ethanol reactors" may have other gene-based abnormalities that cause the accumulation of acetaldehyde following the ingestion of ethanol or ethanol-containing beverages. For example, the surveyed incidence of self-reported ethanol-induced flushing reactions in Scandinavians living in Copenhagen as well as Australians of European descent is about 16% in individuals homozygous for the "normal" ADH1B gene but runs to ~23% in individuals with the ADH1-Arg48His SNP variant; in vitro, this variant metabolizes ethanol rapidly and in humans, it is proposed, may form acetaldehyde at levels that exceed the capacity of ALDH2 to metabolize.[34][36] Notwithstanding such considerations, experts suggest that the large proportion of alcoholic beverage-induced allergic-like symptoms in populations with a low incidence of the glu487lys genotype reflect true allergic reactions to the natural and/or contaminating allergens particularly those in wines and to a lesser extent beers.[33]
Pathophysiology
At low or moderate doses, alcohol acts primarily as a positive allosteric modulator of GABAA. Alcohol also acts as a stimulant in low doses, as it triggers the release of dopamine in the striatum, with this mechanism also being responsible for the compound's interaction with the brain's reward system.[37] Alcohol binds to several different subtypes of GABAA, but not to others. The main subtypes responsible for the subjective effects of alcohol are the α1β3γ2, α5β3γ2, α4β3δ and α6β3δ subtypes, although other subtypes such as α2β3γ2 and α3β3γ2 are also affected. Activation of these receptors causes most of the effects of alcohol such as relaxation and relief from anxiety, sedation, ataxia and increase in appetite and lowering of inhibitions that can cause a tendency toward violence in some people.[38][39][40][41][42][43][44]
Alcohol has a powerful effect on glutamate as well. Alcohol decreases glutamate's ability to bind with NMDA and acts as an antagonist of the NMDA receptor, which plays a critical role in LTP by allowing Ca2+ to enter the cell. These inhibitory effects are thought to be responsible for the "memory blanks" that can occur at levels as low as 0.03% blood level. In addition, reduced glutamate release in the dorsal hippocampus has been linked to spatial memory loss. Chronic alcohol users experience an upregulation of NMDA receptors because the brain is attempting to reestablish homeostasis. When a chronic alcohol user stops drinking for more than 10 hours, apoptosis can occur due to excitotoxicity. The seizures experienced during alcohol abstinence are thought to be a result of this NMDA upregulation. Alteration of NMDA receptor numbers in chronic alcoholics is likely to be responsible for some of the symptoms seen in delirium tremens during severe alcohol withdrawal, such as delirium and hallucinations. Other targets such as sodium channels can also be affected by high doses of alcohol, and alteration in the numbers of these channels in chronic alcoholics is likely to be responsible for as well as other effects such as cardiacarrhythmia. Other targets that are affected by alcohol include cannabinoid, opioid and dopamine receptors, although it is unclear whether alcohol affects these directly or if they are affected by downstream consequences of the GABA/NMDA effects. People with a family history of alcoholism may exhibit genetic differences in the response of their NMDA glutamate receptors as well as the ratios of GABAA subtypes in their brain.[45][46][47][48][49][50][51] Alcohol inhibits sodium-potassium pumps in the cerebellum and this is likely how it corrupts cerebellar computation and body co-ordination.[52][53]
Contrary to popular belief, research suggests that acute exposure to alcohol is not neurotoxic in adults and actually prevents NMDA antagonist-induced neurotoxicity.[54]
Low doses of alcohol (one 360 mL (13 imp fl oz; 12 US fl oz) beer) appear to increase total sleep time and reduce awakening during the night. The sleep-promoting benefits of alcohol dissipate at moderate and higher doses of alcohol.[55] Previous experience with alcohol also influences the extent to which alcohol positively or negatively affects sleep. Under free-choice conditions, in which subjects chose between drinking alcohol or water, inexperienced drinkers were sedated while experienced drinkers were stimulated following alcohol consumption.[56] In insomniacs, moderate doses of alcohol improve sleep maintenance.[57]
Moderate alcohol consumption 30–60 minutes before sleep, although decreasing, disrupts sleep architecture. Rebound effects occur once the alcohol has been largely metabolized, causing late night disruptions in sleep maintenance. Under conditions of moderate alcohol consumption where blood alcohol levels average 0.06–0.08 percent and decrease 0.01–0.02 percent per hour, an alcohol clearance rate of 4–5 hours would coincide with disruptions in sleep maintenance in the second half of an 8-hour sleep episode. In terms of sleep architecture, moderate doses of alcohol facilitate "rebounds" in rapid eye movement (REM) following suppression in REM and stage 1 sleep in the first half of an 8-hour sleep episode, REM and stage 1 sleep increase well beyond baseline in the second half. Moderate doses of alcohol also very quickly increase slow wave sleep (SWS) in the first half of an 8-hour sleep episode. Enhancements in REM sleep and SWS following moderate alcohol consumption are mediated by reductions in glutamatergic activity by adenosine in the central nervous system. In addition, tolerance to changes in sleep maintenance and sleep architecture develops within three days of alcohol consumption before bedtime.
Balance
Alcohol can affect balance by altering the viscosity of the endolymph within the otolithic membrane, the fluid inside the semicircular canals inside the ear. The endolymph surrounds the ampullary cupula which contains hair cells within the semicircular canals. When the head is tilted, the endolymph flows and moves the cupula. The hair cells then bend and send signals to the brain indicating the direction in which the head is tilted. By changing the viscosity of the endolymph to become less dense when alcohol enters the system, the hair cells can move more easily within the ear, which sends the signal to the brain and results in exaggerated and overcompensated movements of body. This can also result in vertigo, or "the spins".[58]
Postprandial triglycerides
Alcohol taken with a meal increases and prolongs postprandial triglyceridemia. This is true despite the observation that the relationship between alcohol consumption and triglyceridemia is "J-shaped," meaning that fasting triglycerides concentration is lower in people who drink 10–20 g/alcohol a day compared to people who either abstain from alcohol or who drink more per day.[59]
Blood pressure
A systematic review reported that alcohol has bi-phasic effect on blood pressure. Both systolic and diastolic blood pressure fell when they were measured couple of hours after alcohol consumption. However, the longer term measurement (20 hours average) showed a modest but statistically significant increase in blood pressure: a 2.7 mmHg rise in systolic blood pressure and 1.4 mmHg rise in diastolic blood pressure.[60] A Cochrane systematic review based on only randomized controlled trials which investigates the acute effect of alcohol consumption in healthy and hypertensive adults is in progress.[61]
Pain
A 2015 literature review found that alcohol administration confers acute pain-inhibitory effects. It also found the relationship between alcohol consumption and pain is curvilinear; moderate alcohol use was associated with positive pain-related outcomes and heavy alcohol use was associated with negative pain-related outcomes.
[62]
^Horowitz M, Maddox A, Bochner M, Wishart J, Bratasiuk R, Collins P, Shearman D (August 1989). "Relationships between gastric emptying of solid and caloric liquid meals and alcohol absorption". The American Journal of Physiology. 257 (2 Pt 1): G291–G298. doi:10.1152/ajpgi.1989.257.2.G291. PMID2764113.
^Jones AW, Holmgren P (July 2003). "Comparison of blood-ethanol concentration in deaths attributed to acute alcohol poisoning and chronic alcoholism". Journal of Forensic Sciences. 48 (4): 874–9. doi:10.1520/JFS2002420. PMID12877310.
^Feige B, Scaal S, Hornyak M, Gann H, Riemann D (January 2007). "Sleep electroencephalographic spectral power after withdrawal from alcohol in alcohol-dependent patients". Alcoholism: Clinical and Experimental Research. 31 (1): 19–27. doi:10.1111/j.1530-0277.2006.00260.x. PMID17207097.
^Andréasson S, Allebeck P (28 February – 6 March 2005). "[Alcohol as medication is no good. More risks than benefits according to a survey of current knowledge]". Läkartidningen. 102 (9): 632–637. PMID15804034.
^Grattan KE, Vogel-Sprott M (February 2001). "Maintaining intentional control of behavior under alcohol". Alcoholism: Clinical and Experimental Research. 25 (2): 192–197. doi:10.1111/j.1530-0277.2001.tb02198.x. PMID11236832.
^"Culture Chemistry and Consequences". Social and Cultural Aspects of Drinking: A report to the European Commission. Oxford UK: Social Issues Research Centre. March 1998.
^Thomasson HR, Beard JD, Li TK (December 1995). "ADH2 gene polymorphisms are determinants of alcohol pharmacokinetics". Alcoholism: Clinical and Experimental Research. 19 (6): 1494–1499. doi:10.1111/j.1530-0277.1995.tb01013.x. PMID8749816.
^Enomoto N, Takase S, Yasuhara M, Takada A (February 1991). "Acetaldehyde metabolism in different aldehyde dehydrogenase-2 genotypes". Alcoholism: Clinical and Experimental Research. 15 (1): 141–144. doi:10.1111/j.1530-0277.1991.tb00532.x. PMID2024727.
^Goedde HW, Agarwal DP, Fritze G, Meier-Tackmann D, Singh S, Beckmann G, et al. (January 1992). "Distribution of ADH2 and ALDH2 genotypes in different populations". Human Genetics. 88 (3): 344–346. doi:10.1007/bf00197271. PMID1733836. S2CID20451607.
^Linneberg A, Fenger RV, Husemoen LL, Vidal C, Vizcaino L, Gonzalez-Quintela A (2010). "Immunoglobulin E sensitization to cross-reactive carbohydrate determinants: epidemiological study of clinical relevance and role of alcohol consumption". International Archives of Allergy and Immunology. 153 (1): 86–94. doi:10.1159/000301583. PMID20357489. S2CID37418991.
^Huang Q, He X, Ma C, Liu R, Yu S, Dayer CA, et al. (January 2000). "Pharmacophore/receptor models for GABA(A)/BzR subtypes (alpha1beta3gamma2, alpha5beta3gamma2, and alpha6beta3gamma2) via a comprehensive ligand-mapping approach". Journal of Medicinal Chemistry. 43 (1): 71–95. doi:10.1021/jm990341r. PMID10633039.
^Platt DM, Duggan A, Spealman RD, Cook JM, Li X, Yin W, Rowlett JK (May 2005). "Contribution of alpha 1GABAA and alpha 5GABAA receptor subtypes to the discriminative stimulus effects of ethanol in squirrel monkeys". The Journal of Pharmacology and Experimental Therapeutics. 313 (2): 658–667. doi:10.1124/jpet.104.080275. PMID15650112. S2CID97681615.
^Duke AN, Platt DM, Cook JM, Huang S, Yin W, Mattingly BA, Rowlett JK (August 2006). "Enhanced sucrose pellet consumption induced by benzodiazepine-type drugs in squirrel monkeys: role of GABAA receptor subtypes". Psychopharmacology. 187 (3): 321–330. doi:10.1007/s00213-006-0431-2. PMID16783540. S2CID32950492.
^Becker HC, Anton RF (January 1989). "The benzodiazepine receptor inverse agonist RO15-4513 exacerbates, but does not precipitate, ethanol withdrawal in mice". Pharmacology, Biochemistry, and Behavior. 32 (1): 163–167. doi:10.1016/0091-3057(89)90227-X. PMID2543989. S2CID6396416.
^Shimizu, A. Matsubara, K. Uezono, T. Kimura, K. Shiono, H. "Reduced dorsal hippocampal glutamate release significantly correlates with the spatial memory deficits produced by benzodiazepines and ethanol". Neuroscience. P 701-706
^Klein G, Gardiwal A, Schaefer A, Panning B, Breitmeier D (September 2007). "Effect of ethanol on cardiac single sodium channel gating". Forensic Science International. 171 (2–3): 131–135. doi:10.1016/j.forsciint.2006.10.012. PMID17129694.
^Shiraishi M, Harris RA (June 2004). "Effects of alcohols and anesthetics on recombinant voltage-gated Na+ channels". The Journal of Pharmacology and Experimental Therapeutics. 309 (3): 987–994. doi:10.1124/jpet.103.064063. PMID14978193. S2CID18823121.
^Farber NB, Heinkel C, Dribben WH, Nemmers B, Jiang X (November 2004). "In the adult CNS, ethanol prevents rather than produces NMDA antagonist-induced neurotoxicity". Brain Research. 1028 (1): 66–74. doi:10.1016/j.brainres.2004.08.065. PMID15518643. S2CID9346522.
^Stone BM (June 1980). "Sleep and low doses of alcohol". Electroencephalography and Clinical Neurophysiology. 48 (6): 706–709. doi:10.1016/0013-4694(80)90427-7. PMID6155259.
^Schuckit MA (February 1994). "Low level of response to alcohol as a predictor of future alcoholism". The American Journal of Psychiatry. 151 (2): 184–189. doi:10.1176/ajp.151.2.184. PMID8296886.
Heberlein U, Wolf FW, Rothenfluh A, Guarnieri DJ (August 2004). "Molecular Genetic Analysis of Ethanol Intoxication in Drosophila melanogaster". Integrative and Comparative Biology. 44 (4): 269–274. CiteSeerX10.1.1.536.262. doi:10.1093/icb/44.4.269. PMID21676709.
Questa voce o sezione sull'argomento sessualità è ritenuta da controllare. Motivo: L'incipit almeno andrebbe riscritto, è in parte scorretto e in parte... strano. I rapporti sessuali possono ovviamente essere non consenzienti e possono non provocare nessun piacere sessuale. Dalla quale può insorgere la riproduzione di nuovi individui è una frase molto strana e parzialmente scorretta (non sono i nuovi individui che si riproducono), che si potrebbe semplificare in per esempio a fini di r…
Artikel ini sebatang kara, artinya tidak ada artikel lain yang memiliki pranala balik ke halaman ini.Bantulah menambah pranala ke artikel ini dari artikel yang berhubungan atau coba peralatan pencari pranala.Tag ini diberikan pada April 2012. Ajeng Anindya (lahir 12 Juli 1990) merupakan seorang atlet sepatu roda berkebangsaan Indonesia. Dia meraih 2 medali emas pada SEA Games 2011 di cabang sepatu roda. Untuk mengasah bakatnya, Ajeng kemudian berguru di klub Eagle. Prestasinya kemudian berkemban…
Lan Mao, sebuah karakter dari Hunan, Tiongkok. Ada usul agar Donghua diganti judulnya dan dipindahkan ke Animasi Tionghoa (Diskusikan). Animasi Tionghoa atau Donghua (Hanzi sederhana: 华人制动画; Hanzi tradisional: 華人製動畫; Hanyu Pinyin: Huárénzhì Dònghuà) merujuk kepada animasi yang dibuat di Tiongkok, Hong Kong, Makau, dan Taiwan. Sejarah Artikel utama: Sejarah animasi Tiongkok Animasi modern Tionghoa dimulai pada 1918 ketika sebuah karya animasi dari Amerika Serikat yang…
يفتقر محتوى هذه المقالة إلى الاستشهاد بمصادر. فضلاً، ساهم في تطوير هذه المقالة من خلال إضافة مصادر موثوق بها. أي معلومات غير موثقة يمكن التشكيك بها وإزالتها. (نوفمبر 2019) كأس الدوري الألماني 2001 تفاصيل الموسم كأس الدوري الألماني النسخة 6 البلد ألمانيا التاريخ بداية:11 …
American politician (1854–1916) For the Canadian composer, see James P. Clarke (composer). James Paul ClarkePresident pro tempore of the United States SenateIn officeMarch 13, 1913 – October 1, 1916Preceded byJacob H. GallingerSucceeded byWillard Saulsbury Jr.United States Senatorfrom ArkansasIn officeMarch 4, 1903 – October 1, 1916Preceded byJames K. JonesSucceeded byWilliam F. Kirby18th Governor of ArkansasIn officeJanuary 8, 1895 – January 12, 1897Preceded byWill…
العلاقات الأسترالية النيجيرية أستراليا نيجيريا أستراليا نيجيريا تعديل مصدري - تعديل العلاقات الأسترالية النيجيرية هي العلاقات الثنائية التي تجمع بين أستراليا ونيجيريا.[1][2][3][4][5] مقارنة بين البلدين هذه مقارنة عامة ومرجعية للدولتين: وج…
Species of bat Narrow-winged pipistrelle Conservation status Least Concern (IUCN 3.1)[1] Scientific classification Domain: Eukaryota Kingdom: Animalia Phylum: Chordata Class: Mammalia Order: Chiroptera Family: Vespertilionidae Genus: Pipistrellus Species: P. stenopterus Binomial name Pipistrellus stenopterusDobson, 1875 The narrow-winged pipistrelle (Pipistrellus stenopterus) is a species of vesper bat. It can be found in Brunei Darussalam, Indonesia, and Malaysia. References …
Human medical condition Medical conditionStiff-person diseasePhotomicrograph of cerebellum with bound anti-GAD65 monoclonal antibodies (green), indirect immunofluorescenceSpecialtyNeurologySymptomsmuscular rigidity and trigger-induced painful muscle spasmsFrequency1 in 1,000,000 Stiff-person syndrome (SPS), also known as stiff-man syndrome,[1] is a rare neurological disorder of unclear cause characterized by progressive muscular rigidity and stiffness. The stiffness primarily affects the…
Artikel ini sebatang kara, artinya tidak ada artikel lain yang memiliki pranala balik ke halaman ini.Bantulah menambah pranala ke artikel ini dari artikel yang berhubungan atau coba peralatan pencari pranala.Tag ini diberikan pada Februari 2023. Fish & Co.IndustriRestoranDidirikan1998KantorpusatSingapuraTokohkunciRicky Choo (pendiri)Lambert Yeo (pendiri)ProdukIkan dan kentang gorengSitus webwww.fish-co.com Fish & Co. adalah sebuah jaringan restoran ikan dan kentang goreng asal Singapura …
Isaak Ėmmanuilovič Babel' Isaak Ėmmanuilovič Babel' (in russo Исаак Эммануилович Бабель?; Odessa, 1º luglio 1894[1] – Mosca, 27 gennaio 1940) è stato un giornalista, drammaturgo e scrittore russo. Indice 1 Biografia 2 Note 3 Bibliografia 4 Voci correlate 5 Altri progetti 6 Collegamenti esterni Biografia Nato da una famiglia ebraica durante un periodo di sommovimenti sociali e di massicci esodi di ebrei dall'Impero russo,[1] Isaak Babel' sopravv…
Kiboud MaulanaLahirBoudewijn Maulana(1938-01-15)15 Januari 1938 Batavia, Hindia BelandaMeninggal6 Juni 2015(2015-06-06) (umur 77)Tangerang, IndonesiaNama lainKiboud MaulanaPekerjaanmusisi JazzTahun aktif1967 - 2015Situs web[1] Boudewijn Maulana (15 Januari 1938 – 6 Juni 2015) dikenal dengan panggilan Kiboud Maulana adalah seorang gitaris Jazz blues asal Indonesia yang juga kakak kandung dari gitaris Ireng Maulana. Perjalanan karier Kiboud pernah bergabung dengan Or…
Horace Greeley for PresidentCampaignU.S. presidential election, 1872CandidateHorace GreeleyBenjamin Gratz BrownAffiliationLiberal RepublicanStatusLost general election In 1872, Horace Greeley ran unsuccessfully for President of the United States. He served as the candidate of both the Democrats and the Liberal Republicans (a breakaway party that split off from the Republican Party due to its members' dislike of the corruption of the Republicans and the Republicans' Reconstruction policies), in t…
2009 Sylvania 300 Race details[1][2][3][4][5] Race 27 of 36 in the 2009 NASCAR Sprint Cup Series Layout of New Hampshire Motor SpeedwayDate September 20, 2009 (2009-09-20)Location New Hampshire Motor Speedway, Loudon, New HampshireCourse Permanent racing facility1.058 mi (1.702 km)Distance 300 laps, 317.4 mi (510.805 km)Weather Mild with temperatures approaching 72 °F (22 °C); wind speeds up to 6 miles per hour (9.7 km/h)Ave…
Major street in west London, England For other uses, see King's Road (disambiguation). King's RoadKing's Road, looking east towards Sloane SquareLength1.9 mi (3.1 km)LocationChelsea, London, EnglandPostal codeSW3, SW6, SW10South endSloane SquareWest endWaterford RoadOtherKnown forShopping, Peter Jones, Saatchi Gallery 213–217 King's Road King's Road or Kings Road (or sometimes the King's Road, especially when it was the king's private road until 1830, or as a colloquialism …
This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed.Find sources: Zarechnaya Nizhny Novgorod Metro – news · newspapers · books · scholar · JSTOR (March 2018) (Learn how and when to remove this message) Nizhny Novgorod Metro Station ZarechnayaЗаречнаяNizhny Novgorod Metro stationGeneral informationLocationLeninsky Di…
Questa voce o sezione sull'argomento Francia non cita le fonti necessarie o quelle presenti sono insufficienti. Puoi migliorare questa voce aggiungendo citazioni da fonti attendibili secondo le linee guida sull'uso delle fonti. Alta Francia Normandia Ile-de-France Grande Est Borgogna-Franca Contea Centro-Valle della Loira Paesi dellaLoira Bretagna Nuova Aquitania Alvernia-Rodano-Alpi Occitania Provenza-Alpi-Costa Azzurra Corsica Guyana Guadalupa Martinica Mayotte Riunione Belgio Lussemburgo…
Evangeline Frances French nota come Evangeline Frances Eva French, in lingua cinese 馮貴珠 (nome alternativo Feng Guizhu 馮貴珠 (1869 – Shaftesbury, 8 luglio 1960) è stata una missionaria britannica protestante che operò in Cina nelle file della Missione della Cina interna (CIM). Indice 1 Biografia 2 Viaggi in Asia centrale 3 Opere 4 Note 5 Collegamenti esterni Biografia Evangeline nacque in Algeria, figlia maggiore di una coppia britannica, John Erington French e sua cugina di primo g…
Герб Румынии Версии Версия, используемая для печатей, и на удостоверениях личности. Детали Утверждён 10 сентября 1992 года11 июля 2016 года (дополнен) Медиафайлы на Викискладе Герб Румынии (рум. Stema României) — государственный символ Румынии, был принят парламентом 10 сентября 1992…
هذه المقالة عن المجموعة العرقية الأتراك وليس عن من يحملون جنسية الجمهورية التركية أتراكTürkler (بالتركية) التعداد الكليالتعداد 70~83 مليون نسمةمناطق الوجود المميزةالبلد القائمة ... تركياألمانياسورياالعراقبلغارياالولايات المتحدةفرنساالمملكة المتحدةهولنداالنمساأسترالياب…