Tag Archives: Receptor (biochemistry)

Histamine, Metabolism, Neuro-excitatory and Neurotransmitters

Role of Histamine, Metabolism, Neuro-excitatory and Neurotransmitters for Addiction

Histamine refers to transmitter that is endogenous in nature and one that is involved in gastric secretions, allergic manifestations and vigilance regulation. It is found in tissues of all animals especially mamma also with high concentrations in the skin, liver and lungs. In the tissues, the transmitter histamine occurs in mast cells which are simply a group of cells whose cytoplasm has high concentrations of basophilic granulations.

In the mast cells histamine exists bonded to acidic compounds like heparin. In most cells with histamine, its production is slow and when it sis depleted t may take several weeks to go back to normal levels. The brain also contains histamine in certain level. Histamine occurs in the brain region in the hypothalamus based o circadian rhythm which occurs in the brain. Its concentration in the plasma does not exceed 1 microgram per liter but this concentration is high in patients suffering from asthma.

neurotransmitters

In the blood the level of histamine ranges from 10 to 100 micrograms in a liter and is primarily concentrated in the basophils. This concentration as studies show rises especially in patients suffering from medical conditions like gastrodudenal ulcers and chronic myelogenous leukemia. Histamine depreciates some times in the body. This means that more has to be produced to replace the one that is lost. This replacement is often slow and can take several weeks. However, histamine renewal in the nervous system and the gastric cells is at faster rate because it is released continuously.

Histamine and Metabolism

Naturally the distribution of histamine in the body is not usually uniform. It however, occurs in in higher concentrations in the mucosa of the gastric system. Its metabolism is dependent on enzymes such as diamine oxidase, histamine N-methyltransferase and histidine decarboxylase. These enzymes seem to be dominant in the stomach region. Studies have been carried out to determine exactly the concentration of histamine in the gastric system. For years this has been a subject of controversial debate and it was only recently that a solution was found. Studies show that the inactivation process of histamine by histamine methyltrasferase takes place in the gastric mucosa that has a significant activity of enzymes.

However it is worthwhile to note that the intestines, liver and spleen have much higher activities which points towards little specification of catabolism of histamine in the gastric mucosa. There have also been debates concerning the activity of diamine oxidase which for years was thought not to exist in the corpus mucosa. Recent studies however, show that moderate enzyme activities of this enzyme is present in some species among them man. In this case then, the metabolism of histamine n the gastric mucosa does not mean its existence in mammalian tissues. Activities of these enzymes could also act as an indication that it has significant physiological functions in the body.

The formation and inactivation of histamine has been shown to be regulated through enzyme activities by during the process of secreting acid. Histamine N-methyltrasferase and histidine decarboxylase are enhanced by gastrin activities and not necessarily influenced by vagal stimulation.

Neuro excitatory and Neurotransmitters for Addiction

Studies show that rugs especially alcohol affect to a great extent the brain as well as some physical processes of the body. There are several reasons that make a person an alcohol addict. These reasons may range from depression, stress, impulse of just mere pleasure. Once a person becomes alcohol dependent, a pattern has already been established and this affects the neural system of the person.

Histamine

The Neurotransmitter Process

In order to fully understand the neurological effects of alcohol addiction in the brain, there is need to understand how the brain transmitters work. The brain communicates through neurons that send messages form ne cells of the brain to an0ther. Transmission of nerve signals takes place from one brain region to another. Once a neuron has been activated, an electrical signal is produced which travels all through the membrane that surrounds the body and axon of the neuron. The signal reaches the end of the neuron and this triggers neurotransmitters to be released from the brain cells. The neurotransmitters then travel from one neuron to another. On reaching the other neuron, the molecules in the transmitter bind with receptors in the neuron and this triggers new electric signal to be produced. Production of new signals depends on the type of neurotransmitter that is involved in the process.

Most neurotransmitters exhibit inhibitory and excitatory effects. This is dependent on the region of the brain and the receptors present in that region. Neurotransmitters with excitatory effects include among others glutamate, dopamine and serotonin while those with inhibitory effects include gamma-aminobutyric acid most commonly referred to as GABA. When one takes alcohol it tends to reinforce the transmitter system. This affects many neural transmitter processes which trigger some long term effects like withdrawal, tolerance, dependence, sensitization and finally addiction.

This information can be found for free at www.awaremednetwork.com. Here you will also find other health and awareness tips.

Role of Histamine, Metabolism, Neuro-excitatory and Neurotransmitters for Addiction

 

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Endogenous Opioids

Endogenous Opioids and Opioid Receptors

endogenous opioidsThe term opioids are not new to many, it has been heard as the media is always abreast with all information about these opioid drugs which to the public are known mostly for the wrong reasons. People have got misinformed about these drugs so much that when you tell a layman that these drugs are used in hospital then to him you will something much worse than an alien. However to the medical fraternity these opioids are essentials that are hard to survive without. That said and left, back to the topic; Endogenous Opioids is a new term to many and if your prediction is as right as mine then you are hearing it for the first time. What does it really mean? The endogenous opioids are opiate-like substance, such as an endorphin, produced by the body. If you thought that you can live without these endogenous opioids then you need to wake up from your momentary slumber. Every day of our lives we face pain of all sorts even the most insignificant pains needs the actions of these opioids to give you peace.

Today, the endogenous opioid system is one of the most studied innate pain-relieving systems. The endogenous opioid system consists of widely scattered neurons that produce three opioids: beta-endorphin, the met- and leu-enkephalins, and the dynorphins. These opioids act as neurotransmitters and neuromodulators at three major classes of receptors, termed mu, delta, and kappa, and produce analgesia. The endogenous opioids works in the same manner as the narcotic opioids in that they bind to the same receptors and they also have both good and negative effects. There might be all sorts of information out there that you can lay your hands that may speak well of the opioids but the bitter truth is we all depend on despite the negative light they have been portrayed in.We are all naturally dependent on opioids for our emotional health. Both narcotics and internally generated endogenous opioids exert their action on the body by interacting with specific membrane receptor-proteins on our nerve cells.

There are three large pro-compounds that are produced by the body and these are: proenkephalin, prodynorphin, and pro-opiomelanocortin. However, endorphins can further decompose to small fragments, oligomers, which are still active. Oligomers pass the blood-brain barrier more readily. Enzymatic degradation of small-chain endorphins is accomplished by dipeptidyl carboxypeptidase, enkephalinases, angiotensinases, and other enzymes. This limits their lifetime in the unbound state.

Presynaptically opioid receptors inhibit transmission of excitatory pathways. These pathways include acetylcholine, the catecholamines, serotonin, and substance P. Substance P is a neuropeptide active in neurons that mediate our sense of pain. Endogenous opioids are also involved in glucose regulation. Opioid receptors are functionally designated as mu, delta, kappa among others. These categories can be further sub-classified by function or structure. Decoding the human genome has allowed the genetic switching-mechanisms that control the expression of each opioid receptor to be determined at the transcriptional and post-transcriptional level.

Opioid-driven inhibition of neuronal excitability is mediated by the activation of a variety of potassium channels in the plasma membrane. The disparate subjective and behavioral effects evoked by activation of the different categories of opioid receptor are typically not the outcome of different cellular responses, but reflect the different anatomical distributions of each receptor. Unlike kappa opioid receptors, however, both mu and delta opioid receptors internalize on exposure to agonists. Activation of any type of opioid receptor inhibits adenylate cyclase, resulting in a fall in intracellular cAMP and diminished action potential firing. This causes a reduced flow of nociceptive information to the brain. Conversely, opioid addicts undergoing withdrawal suffer elevated cAMP levels and enhanced protein kinase A activity, resulting in increased neurotransmitter release.

Role of Mu receptors in addiction

The Mu opioid receptors are the gateway to addiction. This is because they mediate positive reinforcement following direct or indirect activation. In an experiment where mice without mu receptors were used, it was found that the morphine’s analgesic and addictive properties are abolished in these mice. This shows that mu receptors mediate both the therapeutic and the adverse activities of opioids. The mice that were lacking mu receptors were found to lack of morphine-induced analgesia, reward, and dependence. The mice had increased sensitivity to pain. This shows that the mu receptors play a critical role in addiction. These mu receptors function as switches upon direct or indirect reinforcement of opioid abuse. Mu-opioid receptors are a key molecular switch triggering brain reward systems and potentially initiating addictive behaviors. The lack of mu-receptors abolishes the analgesic effect of morphine, as well as place-preference activity and physical dependence. This receptor therefore mediates therapeutic analgesia and adverse activities of morphine.

Opioid withdrawal symptom

endogenous opioidsWhen a person has been using the opioids for some time, he will become physically adapted to the drugs so much that when he stops abruptly he will experience the symptoms of withdrawal. Withdrawal is not only faced by opioid user only but also other sick people who are on other drugs as well. However to limit the withdrawal symptoms, there are some factors that come in handy. One of these factors is the pace and how you exit from using these drugs. Your doctor will be of help in helping you by developing safe exit strategies that will limit the withdrawal symptoms.

Finally, you need more information to stay away from dependence on alcohol and drugs as these have crippled societies and that is why here at AWAREmed we are dedicated to finding the best solutions to addiction and dependence on substances. Dr. Dalal Akoury (MD) is always in the mood of helping any patient to be addiction free. Do not hesitate to call on her for help in managing any sort of chronic pain or any type of addiction as well as other diseases.

Endogenous Opioids and Opioid Receptors

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