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Law school symptoms and conditions

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50 Side Effects posted for law school

April 21th
2008
10:47 AM

Why the brain function is impaired due to Singulair????? Maybe.

Here is the last chapter in a theoretical reason why Singulair affects brain function thus causing anxiety, depression, agitation, aggression, ADD/ADHD, and in extreme situations maybe seizures. I presented the study of the Chinese researchers that show a direct link between the cysLT1 receptor and the astrocyte in the brain. We don't really know how the cysLT1 receptor interacts with receptors that control astrocytes under all circumstances. We just know that there is an important link.

So last night, I had a dream about astrocytes. I don't really have anything to do but sit on an island, look at the Caribbean and fish so mental stimulation is actually welcome.

The last part of the "chain reaction" is probably the astrocytes role in glyconeogenesis. In other words, when the brain does not get proper nutrition, it sends signals to the liver to do something about the problem. The liver in turn releases glycogen which is turned into glucose to be released into the blood stream. A very unhappy brain becomes a very relieved brain. Obviously, we can't be eating all day long to keep our blood sugar up so the liver has to store energy and release it at the correct time.

Here is a diagram of that. Astrocytes are the only cell that produce the proper chemicals for this process to happen.

http://www.nature.com/jcbfm/journal/v27/n2/fig_tab/9600343f5.html
FIGURE
Quote: All credit to the authors, of course.

Energy metabolism in astrocytes: high rate of oxidative metabolism and spatiotemporal dependence on glycolysis/glycogenolysis
Leif Hertz, Liang Peng and Gerald A Dienel

BACK TO ARTICLEFigure 5.
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Glucose utilization pathways that provide or consume ATP. (A) Schematic of key aspects of the glycolytic pathway of glucose utilization for energy metabolism and major branch points that can divert carbon for other uses, including NADPH generation, storage of glucosyl units in glycogen, neuromodulator, and amino acid and nucleotide biosynthesis. The most important reactions for generation of energy are glycolysis (pyruvate/lactate formation from glucose), shown in light brown and occurring in all cell types, and glycogenolysis (pyruvate/lactate formation from glycogen), shown in light green, which occurs only in astrocytes, due to the astrocyte-specific expression of the enzyme glycogen phosphorylase, which releases a glucosyl unit from glycogen as G1P. The energetically most important biosynthetic reactions are synthesis of glycogen from glucose (glycogenesis) shown in brown and green and from pyruvate/lactate (gluconeogenesis) shown in pink, brown, and green. Gluconeogenesis is also astrocyte-specific, because only astrocytes express fructose-1, 6-bisphosphatase, which generates F6P from fructose-1, 6-bisphosphate (F1, 6P) and PC, which generates oxaloacetate (OAA) from pyruvate. The latter reaction is followed by formation of phosphoenolpyruvate (PEP) by decarboxylation of OAA; this sequence is necessary to form PEP from pyruvate, an energetically unfavorable reaction. Biosynthesis of serine/glycine (shown in olive) is also an astrocyte-specific process due to preferential expression of 3-phosphoglycerate dehydrogenase (Yamasaki et al., 2001). Both neurons and astrocytes form alanine and ribose-5-phosphate (R5P), the latter in the pentose shunt pathway (upper left corner), linked to NADPH production needed for operation of glutathione peroxidase and oxidation of monoamine transmitters. The MAS, indicated by red, transfers malate formed in the cytosol from oxaloacetate during conversion of NADH to NAD+ into mitochondria. PDH-mediated formation of acetyl CoA, which is also shown in red, initiates oxidative degradation of pyruvate in the mitochondria. Red and blue text for ATP indicates energy production and utilization, respectively. (B) Major reactions and net ATP yields or net ATP consumption of major pathways derived from the glycolytic pathway are indicated in color-coded boxes that correspond to the color-coded pathways in panel A. For simplicity, the scheme indicates the energy yields (ATP) and NAD(P)H production or utilization based on metabolism of 1 glucose to form one ribulose-5-P, two lactate/pyruvate, or 2 serine; a similar representation illustrates the energy and cofactors required for gluconeogenic conversion of two moles of lactate into one free (G6P) or glycogen-bound glucosyl unit. Glc, glucose; P, phosphate; G6P, glucose-6-P; 6PG, 6-P-gluconate; R5P, ribulose-5-P; GSH, reduced form of glutathione; GSSG, oxidized form of glutathione; F6P, fructose-6-P; F1, 6-P, fructose-1, 6-bisphosphate; GAP, glyceraldehyde-3-P; DHAP, dihydroxyacetone-P; 3PG, 3-P-glycerate; 2PG, 2-P-glycerate; PEP, phosphoenolpyruvate; Pyr, pyruvate; Lac, lactate; Ala, alanine; OAA, oxaloacetate; 3P-HyPyr, 3-P-hydoxypyruvate; Glu, glutamate; KG, -ketoglutarate; 3P-L-Ser, 3P-L-serine; L-ser, L-serine; D-ser, D-serine; Gly, glycine; C1, one carbon fragment used for methyl donor reactions.

This is quite interesting because should the connection between the cysLT1 receptor and astrocyte be established and explained, it shows that there is a very direct link between the immune system and metabolism. That should be intuitive because when we get seriously sick, then we are laying in bed and the body should try to conserve energy so that we don't just waste away.

So what happens if we cause changes in the cysLT1 receptor to cause the astrocytes to believe that we are sick, the normal connection between the brain and glyconeogenesis then doesn't exist. We would have to be causing some kind of periods of extreme stress on the brain because we are out moving around and doing not home sick in bed.

Maybe we should award the Chinese researchers the nobel prize? Maybe they established the connection between the immune system and metabolism? Is there also a link between the immune system of some individuals and depression? Some how, this makes perfect sense. So we have to find out and help as many people as we can.

I think that it is time to call the lawyer-biochemists to find out if this can be proven to be true and if Merck knew or not.

-- By concernedcitizen | Reply | (3) replies | Private Message me

April 15th
2008
11:49 AM

I have read many posts about Adderall XR side effects, and wondered if anyone has found another medicine that works better for them. My 12 year old daughter is taking 20mg/day of Adderall XR. It definitely helps her tremendously in focusing at school, but the side effects are just too much. (she has huge mood swings, verbal tics, compulsive hair plucking, etc.) We need an alternative ASAP. If you have something else that you recommend, please let me know. Thanks!

-- By fldad | Reply | (2) replies | Private Message me

March 29th
2008
11:11 AM

CANNOT STOP CRYING - I started taking Singulair one month ago. I'm a 28 year old female in her last semester of law school. I'm naturally neurotic and high strung, but I usually only cry one week out of the month. That week came and went and I still tear up at the drop of a hat. I watched a youtube Earth Hour video today and had to choke back tears so my husband wouldn't see them. My aunt mentioned Singulair's link to depression yesterday, so I decided to check it out. OH MY GOD! Is this medicine the reason I cried watching a trial the other day? Did this medicine cause me to lay in bed the other morning paralyzed with paranoia about school? I had to talk myself out of bed, and then I spent the rest of the day wondering if my mock trial partner hated me. ANOTHER NOTE - I thought it was the best allergy drug in the world when I started taking it last month, but I did notice that the pressure settled in my chest instead of my head. I'm now on my second round of antibiotics trying to kill the infection in my chest. Hmmm. I guess it's back to being miserable from mountain cedar - better than crying every time I watch a Save the Children commercial.

-- By jmelee66 | Reply | Private Message me

March 24th
2008
6:29 AM

I've been on Tri-Sprintec for a month and a half. My husband is going crazy due to my mood swings. Of course he gets the brunt of it compared to anybody else. One moment I am fine and the next I am yelling because I dropped the butter on the floor. Ten minutes later I've forgotten this instance and I'm crying for no apparent reason. I normally have normal to dry skin, and no acne (to very few) Lately my face is very itchy and I've had a lot of breakouts. I work in Law Enforcement, and have no problems with being straight forward and pushy, but lately I don't have it in me, I feel very depressed and a lot of self doubt. I also don't have a big appetite, I feel nauseas, and I do take the pill with food. I've also gained 10 pounds in the last month and a half. I don't know if this is a coincidence or if it's side effects from the birth control. I have also had a lot of headaches lately.

-- By tazeygal4life | Reply | (2) replies | Private Message me

August 23th
2007
5:14 AM

I have been on Coumadin for about 2 months now after surviving a cerebral sinus venous thrombosis (blood clot on my brain - akin to a stroke). I am s 34 yo female who races triathlons and leads a very active healthy lifestyle. My side effects seem to be mild compared to what I read of others. I am on 5mg/day, except 1 day a week I take 10mg. My INR has been pretty stable. The side effects I notice are mild forgetfulness which I am hoping goes away as I start my 3rd year of law school next week! I also had some weird skin peeling on my hands, but that has subsided. I seem to urinate more often than normal and soda pop tastes weird to me now. Anyone else experience the frequent urination and/or taste issues?
Thanks!
Dana :)

-- By cyclejunkie | Reply | (2) replies | Private Message me

September 21th
2006
11:35 AM

OH MY GOD. I'm sitting here crying. I was on Yasmin for 3 years when I was engaged. When we broke up I went off it - i figured i didn't need to put hormones in my body if I wasn't having sex (i needed a break from that too!). plus who needs to spend the money. i had been anxious and depressed for years and thought it was the relationship, work, law school, the bar exam, etc..... i went into therapy after the break up and started to feel better.

well, it's been 10 months and i felt fantastic. lost a bunch of weight, met a great new guy, work is great, happy happy. went back on yasmin. all of a sudden i'm anxious and paranoid and miserable. that knot between my shoulder blades is back. my sex drive is gone. i've gained 5 lbs in 3 weeks but i'm not eating more. no sex is worth this.

I'VE TAKEN MY LAST YASMIN. THANK YOU!!!!!

Kari

-- By kbsesquire | Reply | Private Message me

July 18th
2003
7:27 PM

Since starting levoxly i have been to the emergency room twice for heart palpitations and chest pains, my doctor says everything is in range but i lower the medication as i lose weight and the lab results are the same with and as i lower it the palipitations stop, my doctor tells me this isn't the medication because i am in "normal range" but i know it is, they are simple cause and effect. when i get palpitations as i lose weight, i lower it and they stop. I am in law school, i have had a complete inability to concentrate and flunked out of my first year, i'm not sleeping and eating is hard because i am so naseus, i don't think that our doctors realize what this is doing to us!

-- By tlgb1 | Reply | Private Message me


 

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