Depression alcohol

As for abused substances, the question is usually, Which came first Is the alcoholic depressed because of his drinking or does he drink because he is depressed The answer is usually both. The key is that to treat one you must treat the other. Simply giving an antidepressant to a depressed substance abuser accomplishes little. 

Nieminen LR, Makino KK, Mehta N, Virkkunen M, Kim HY, Hibbeln JR. Relationship between omega-3 fatty acids and plasma neuroactive steroids in alcoholism, depression and controls. Prostaglandins, Leukotrienes, Essential Fatty Acids 2006 75 309-314. 

Peripheral vasodilatation. Alcohol depresses the vasomotor centre and this accounts for the feeling... 

Worsens symptoms e.g. cannabis - paranoia alcohol - depression ... 

As explained above, ethanol is essentially a cenhal nervous system (CNS) depressant dmg although mesolimbic dopamine neurones display increased activity. The effect in this latter case may be through inhibition of an inhibitory pathway. Generally however, alcohol depresses higher cortical function which in turn leads to a sense of relaxation, a loss of self restraint and uninhibited behaviour. This initial effect is followed by progressively increasing depression of all neuronal activity. Higher mental functions mediated by areas like the frontal cortex... 

Interaction of Solids With Flotation Reagents. For flotation to occur with the aid of reagents, such compounds must adsorb at the sohd—hquid interface unless the soHd to be floated is naturally hydrophobic. In this latter case only depression can be attempted by the use of additional ions or depressants that hinder bubble—particle adhesion. Frothers (typically long-chain alcohols) and/or modifying agents such as hydrocarbon oils can, however, be used to enhance the collection of naturally hydrophobic soflds such as M0S2, talc, or plastics. 

Toxicity studies on trifluoroethanol show acute oral LD q, 240 mg/kg acute dermal LD q, 1680 mg/kg and acute inhalation L(ct) Q, 4600 ppmh. Long-term subchronic inhalation exposure to 50—150 ppm of the alcohol has caused testicular depression in male rats, but no effects were noted at the 10 ppm level (32). Although the significance of the latter observations for human safety is unknown, it is recommended that continuous exposure to greater than 5 ppm or skin contact with it be avoided. 

Physical properties of glycerol are shown in Table 1. Glycerol is completely soluble in water and alcohol, slightly soluble in diethyl ether, ethyl acetate, and dioxane, and insoluble in hydrocarbons (1). Glycerol is seldom seen in the crystallised state because of its tendency to supercool and its pronounced freesing point depression when mixed with water. A mixture of 66.7% glycerol, 33.3% water forms a eutectic mixture with a freesing point of —46.5°C. 

The molten carbonate fuel ceU uses eutectic blends of Hthium and potassium carbonates as the electrolyte. A special grade of Hthium carbonate is used in treatment of affective mental (mood) disorders, including clinical depression and bipolar disorders. Lithium has also been evaluated in treatment of schizophrenia, schizoaffective disorders, alcoholism, and periodic aggressive behavior (56). 

Like brines, alcohols were readily available and widely used as antifreeze Hquids in the early 1900s. Both methanol and ethanol offer exceUent heat transfer and efficient freeze point depression. However, the alcohols have the distinct disadvantage of their low boiling points. During the summer months when the engines operate hot, significant amounts of the alcohols are lost because of evaporation. These evaporative losses result in cosdy make-up requirements. Additionally, the alcohols have very low flash points and potentially flammable vapors. These safety concerns have, particularly in recent years, caused the use of alcohols to be completely discontinued for most heat-transfer systems. 

Overexposure to tetrachloroethylene by inhalation affects the central nervous system and the Hver. Dizziness, headache, confusion, nausea, and eye and mucous tissue irritation occur during prolonged exposure to vapor concentrations of 200 ppm (15). These effects are intensified and include incoordination and dmnkenness at concentrations in excess of 600 ppm. At concentrations in excess of 1000 ppm the anesthetic and respiratory depression effects can cause unconsciousness and death. A single, brief exposure to concentrations above 6000 ppm can be immediately dangerous to life. Reversible changes to the Hver have been reported foUowing prolonged exposures to concentrations in excess of 200 ppm (16—22). Alcohol consumed before or after exposure may increase adverse effects. 

The pH of the pulp to the flotation cells is carefliUy controlled by the addition of lime, which optimizes the action of all reagents and is used to depress pyrite. A frother, such as pine oil or a long-chain alcohol, is added to produce the froth, an important part of the flotation process. The ore minerals, coated with an oily collected layer, are hydrophobic and collect on the air bubbles the desired minerals float while the gangue sinks. Typical collectors are xanthates, dithiophosphates, or xanthate derivatives, whereas typical depressants are calcium or sodium cyanide [143-33-9] NaCN, andlime. 

Glycerol, Glycol, and Other Polyhydnc Alcohols. These alcohols (Class 3, regenerative) are widely used to dry gases (20,21). However, they can only produce dew points in the range of —15 to 0°C (see Antifreezes and deicing fluids). They have somewhat lower capacity than sulfuric acid (Fig. 2) but are effective when either injected or employed in a multistage contactor to achieve dew point depression. 

Because alcohol intoxication may be simulated by many pathologic conditions, including diabetic acidosis, the postconvulsive depression of epilepsy, uremia, head injuries, and poisonings by any other central nervous depressant and some stimulants (280), a diagnosis of acute alcoholism should not be made casually chemical testing of blood, urine, or expired air is always desirable. 

As regards toxicity, pyrazole itself induced hyperplasia of the thyroid, hepatomegaly, atrophy of the testis, anemia and bone marrow depression in rats and mice (72E1198). The 4-methyl derivative is well tolerated and may be more useful than pyrazole for pharmacological and metabolic studies of inhibition of ethanol metabolism. It has been shown (79MI40404) that administration of pyrazole or ethanol to rats had only moderate effects on the liver, but combined treatment resulted in severe hepatotoxic effects with liver necrosis. The fact that pyrazole strongly intensified the toxic effects of ethanol is due to inhibition of the enzymes involved in alcohol oxidation (Section 4.04.4.1.1). 

Solvents acetone, methyl ethyl ketone (MEK), toluene, xylene, glycol, ethers, alcohol defats and dries skin some may be absorbed may carry other components through skin high volatility, exposure possible irritation central nervous system depression (e.g. dizziness, loss of coordination) low to high toxicity, longterm effects... 

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