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What neurological condition is caused by inhibiting GABA?

When GABA is inhibited in the brain, it leads to a neurological condition called  epilepsy.  This happens because GABA normally controls brain activity by stopping too much nerve signalling. When GABA is not working properly, the brain loses its balance and nerve cells start becoming overactive. This overactivity can lead to  seizures,  which is the main feature of  epilepsy. Seizures  are sudden, uncontrolled electrical disturbances in the brain that can cause changes in behavior, movements, feelings, or consciousness. They may last from a few seconds to minutes and can be caused by epilepsy, fever, head injury, or other neurological conditions. Seizures vary in type and severity. Step-by-Step Explanation: How GABA Inhibition Leads to Epilepsy To understand how epilepsy is caused by inhibiting GABA, we can break the process into simple steps. These steps explain what GABA normally does, what changes happen when it is blocked and how those changes result in...

Which neurological disorders are linked to increase dopamine secretion?

Dopamine is a crucial neurotransmitter in the brain that plays a significant role in controlling motor functions, emotional responses and reward pathways. It is involved in regulating mood, movement and several other physiological processes. However, when there is an imbalance in dopamine secretion or its activity, it can lead to several neurological and neuropsychiatric disorders. An increase in dopamine activity is linked to certain disorders, where excessive dopamine levels in specific brain regions can lead to abnormal behaviors and symptoms. Here are two neurological disorders closely associated with increased dopamine secretion: 1. Tourette Syndrome Tourette Syndrome (TS) is a neurological disorder characterized by repetitive, involuntary movements (motor tics) and sounds (vocal tics). It often begins in childhood and can persist into adulthood. In individuals with Tourette Syndrome, there is evidence of increased dopamine activity, particularly in the  basal ganglia,  a...

Write the name of neurotransmitter which act as neuromodulator as well as inhibitor of neurotransmitter

One of the best-known neurotransmitters that shows both neuromodulatory and inhibitory functions is  GABA (Gamma-Aminobutyric Acid).  It is a major chemical messenger in the central nervous system (CNS) and plays a vital role in regulating brain activity. GABA is unique because it not only participates in fast synaptic transmission as an inhibitory neurotransmitter but also acts more broadly as a neuromodulator that controls the excitability of entire neural circuits. 1. GABA as a Neuromodulator As a neuromodulator, GABA works at a slower and more widespread level than fast synaptic transmission. Instead of targeting a single postsynaptic neuron, it can influence large groups of neurons or entire regions of the brain. Neuromodulatory action of GABA usually happens through GABA-B receptors, which are metabotropic and linked with second messenger systems. Through these pathways, GABA can regulate the activity of other neurotransmitter systems like: Glutamate (main excitatory neu...

Which hormone is called as sleep hormone?

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The hormone that is called the sleep hormone is  Melatonin.  It is a naturally occurring hormone in the human body that controls the sleep-wake cycle, also known as the  circadian rhythm.  Melatonin is secreted by the  pineal gland,  which is a small, cone-shaped endocrine gland located deep in the brain, near the centre, just above the cerebellum and behind the third ventricle. Melatonin secretion is directly controlled by the amount of light the eyes receive. When the environment becomes dark, the retina sends signals to a special region in the hypothalamus known as the  suprachiasmatic nucleus (SCN).  This SCN then sends nerve signals to the pineal gland, which begins to release melatonin into the bloodstream. The rise in melatonin levels at night makes a person feel sleepy and relaxed, preparing the body for sleep. During the daytime, especially in the presence of sunlight or artificial light, melatonin secretion is stopped. This is why melato...

Write the name of two glands are the main secretary gland of brain

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The brain is not only the central organ of the nervous system but also contains two major secretory glands that are directly involved in endocrine functions. These are: Pituitary gland (Hypophysis) Pineal gland (Epiphysis cerebri) These glands are part of the neuroendocrine system, which links the brain and hormonal regulation. They help in maintaining homeostasis, regulating growth, metabolism, stress response, sleep cycle, reproduction and many other vital processes. 1. Pituitary Gland: The Master Gland The pituitary gland is called the  "master gland"  because it controls the activity of almost all other endocrine glands in the body. It is located at the base of the brain, in a bony cavity called the sella turcica of the sphenoid bone. It is connected to the  hypothalamus  by a stalk called the  infundibulum,  which carries signals from the brain to control hormone secretion. The pituitary gland has two main lobes: i. Anterior Pituitary (Adenohypophysis)...

Explain the steps involved in retrograde transport

Retrograde transport is a process by which proteins and membranes are moved backward i.e., from later compartments to earlier ones within the endomembrane system. This transport mechanism plays an essential role in maintaining organelle identity, recycling transport machinery and retrieving specific proteins that need to return to their origin for reuse. It is important to understand from the beginning that retrograde transport is  not limited  to the retrieval of proteins from the Golgi apparatus back to the endoplasmic reticulum (ER). It also operates actively between endosomes and the Golgi, especially in the recycling of mannose-6-phosphate receptors (M6PRs). These receptors, after delivering lysosomal enzymes to endosomes, must return to the trans-Golgi network (TGN) to participate in another round of sorting. This ensures a continuous and efficient targeting of lysosomal enzymes. Retrograde transport is a multi-step process, usually involving four main steps, which toget...

Explain the steps involved in anterograde transport

Anterograde transport refers to the forward movement of proteins and lipids from the endoplasmic reticulum (ER) towards their final destinations, such as the Golgi apparatus, plasma membrane, or extracellular space. This process is a highly regulated and directional pathway, which ensures that proteins follow a proper route, allowing cells to maintain organisation, compartmentalisation and functional efficiency. The transport is carried out using vesicles, and involves several organelles and protein complexes working in coordination. This process can be described in five major steps, beginning in the rough ER and progressing toward the cell membrane or beyond: Step 1: Protein Synthesis and Folding in the Rough ER Anterograde transport begins with the synthesis of proteins on membrane-bound ribosomes of the rough ER. As the proteins are translated, they are inserted into the ER lumen or membrane. Within the ER, they undergo initial folding, assembly, and modifications, including N-linke...

Explain the targeting of soluble lysosomal proteins to endosomes and lysosomes

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The targeting of soluble lysosomal proteins, such as hydrolytic enzymes, to endosomes and lysosomes is a well-organised and highly regulated process. This mechanism ensures that such enzymes reach the lysosomes accurately, where they are needed for intracellular digestion, and are not secreted outside the cell. This entire process takes place through a series of interconnected steps, involving specific molecular signals, vesicle formation and organelle targeting, which begins in the rough endoplasmic reticulum (RER) and ends in the lysosome. Step 1: Synthesis in the Rough Endoplasmic Reticulum (RER) Soluble lysosomal enzymes are synthesised by ribosomes attached to the rough ER. As the mRNA is translated, the growing polypeptide is inserted into the ER lumen. Inside the ER, these proteins are properly folded and undergo N-linked glycosylation, which prepares them for further modifications in the Golgi. Step 2: Transfer to the Golgi Apparatus From the ER, the glycosylated proteins are t...

Explain the role of the ER and Golgi Complex in protein trafficking

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In eukaryotic cells, protein trafficking is a highly regulated and stepwise process that ensures proteins reach their correct destination either within the cell or outside of it. Two major organelles that perform central roles in this process are the  Endoplasmic Reticulum (ER) and the Golgi Complex.  Together, these organelles carry out multiple interconnected functions such as protein synthesis, folding, quality control, modification, sorting, and vesicle-mediated transport. Their roles are highly coordinated and form the backbone of the endomembrane trafficking system. Role of the Endoplasmic Reticulum (ER) The ER is the first organelle involved in the protein trafficking pathway. It exists in two forms, rough ER (RER) and smooth ER (SER). Among these, the rough ER is primarily involved in protein trafficking. It is called "rough" because it is studded with ribosomes, which are the sites of protein synthesis. The RER plays several important roles in protein trafficking: Sy...

Describe the endomembrane system

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The endomembrane system is a group of interconnected membrane-bound organelles found in eukaryotic cells. This system is responsible for the synthesis, modification, transport, and sorting of proteins and lipids within the cell. All organelles in this system are either physically connected or communicate with each other through vesicle-mediated transport. This system helps in maintaining the organisation, compartmentalisation and communication between different parts of the cell. The word "endomembrane" means "within the membrane" and this system is very important for keeping the cell functioning smoothly. Main Components of the Endomembrane System There are six major components that make up the endomembrane system. These are: 1. Nuclear Envelope The nuclear envelope is a double membrane that surrounds the nucleus. It contains nuclear pores that allow the controlled exchange of materials (like mRNA and proteins) between the nucleus and the cytoplasm. Its outer membr...

Describe the step involved in the trafficking of soluble lysosomal enzymes from the trans-Golgi network and cell surface to lysosomes

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The trafficking of soluble lysosomal enzymes from the trans-Golgi network (TGN) and sometimes the cell surface to the lysosomes is a highly regulated, multistep process. This mechanism ensures that lysosomal hydrolases are specifically recognized, sorted and delivered to their correct destination without getting misdirected or secreted. This sorting is based mainly on mannose-6-phosphate (M6P) tags present on the enzymes, which act as a signal for targeting. There are five major steps in this trafficking pathway: 1. Tagging with Mannose-6-Phosphate in the Golgi Apparatus Soluble lysosomal enzymes are first synthesized in the rough endoplasmic reticulum (RER) and transported to the cis-Golgi. Inside the Golgi, they are modified by a two-step enzymatic reaction: An enzyme called  N-acetylglucosamine-1-phosphotransferase  attaches a phosphorylated N-acetylglucosamine (GlcNAc-P) group to the mannose residue of the N-linked oligosaccharides on the enzyme. Another enzyme removes the...

What is the role of a mannose 6-phosphate residues in the sorting of protein?

Mannose-6-phosphate (M6P) residues play a critical role in the targeting and sorting of lysosomal enzymes from the trans-Golgi network to the lysosomes. This is one of the most well-known examples of protein sorting signals that help direct enzymes to their correct destination inside the cell. Lysosomes are cellular organelles responsible for breaking down macromolecules with the help of hydrolytic enzymes. These enzymes are synthesized in the rough endoplasmic reticulum (RER) and pass through the Golgi apparatus before reaching the lysosomes. However, they do not go to the lysosomes randomly. They are specifically tagged with mannose-6-phosphate residues, which act like an "address label" for lysosomal targeting. The process involves the following key steps: 1. Addition of Mannose-6-Phosphate in the Golgi: After synthesis in the RER, lysosomal enzymes enter the cis-Golgi, where they undergo post-translational modification. In the cis and medial Golgi, a special enzyme called...

Describe the types of coated vesicles and their functions

Coated vesicles are specialized membrane-bound carriers used for transporting proteins and lipids between different compartments inside the cell. They are called  "coated"  because their outer membrane is covered by specific protein coats that help in vesicle formation, cargo selection and targeting. There are three main types of coated vesicles: clathrin-coated, COPI-coated and COPII-coated vesicles. Each type is associated with a particular direction and function of transport. 1. Clathrin-Coated Vesicles Clathrin-coated vesicles are among the most extensively studied vesicles. These are mainly involved in transport between the trans-Golgi network, endosomes and the plasma membrane. Mechanism: Clathrin forms a unique structure made of three-legged units known as  triskelions,  which assemble into a lattice-like cage around the budding vesicle. This coat provides mechanical support and helps in vesicle formation. Clathrin works together with adaptor proteins, such as...

Describe the molecular mechanism of vasecular traffic

Vesicular traffic refers to the highly coordinated process by which proteins and lipids are transported between different compartments within the eukaryotic cell using membrane-bound vesicles. This mechanism is essential for maintaining compartmental identity, delivering newly synthesized proteins to their proper destinations, recycling membrane components and internalizing extracellular materials. The molecular mechanism of vesicular transport involves four key steps: vesicle formation, targeting, docking and fusion. 1. Vesicle Formation: The process begins at the donor membrane, where  cargo molecules  (proteins or lipids) are selected and packaged into transport vesicles. This step is mediated by coat proteins such as COPI, COPII and clathrin, which help in shaping the vesicle and selecting specific cargo. COPII-coated vesicles  transport proteins from the endoplasmic reticulum (ER) to the Golgi apparatus. COPI-coated vesicles  are involved in retrograde transport...

Differentiate between secretory and endocytic pathways of protein sorting

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Protein sorting in eukaryotic cells occurs through two major pathways,  the secretory pathway and the endocytic pathway.  Both are essential for maintaining intracellular organization, membrane composition, and regulated transport of proteins and other molecules. Both the secretory and endocytic pathways involve vesicular transport and share certain components but they differ fundamentally in their transport direction, functional role, origin and final destination within the cell. 1. Based on Definition and Direction of Transport The secretory pathway is a biosynthetic and outward pathway that transports newly synthesized proteins from the endoplasmic reticulum (ER) to the Golgi apparatus and finally to the plasma membrane or extracellular space. This pathway is responsible for the secretion of proteins and insertion of membrane proteins. In contrast, the endocytic pathway is an inward transport pathway where materials such as membrane proteins, fluids and macromolecules are i...

Explain the sorting of proteins to mitochondria

The sorting of proteins to mitochondria is an essential and complex process that ensures proteins synthesized in the cytoplasm reach their correct mitochondrial locations. Mitochondria have their own small genome, but most of their proteins are encoded by the nuclear genome. These nuclear-encoded proteins are synthesized in the cytoplasm and must be imported into the mitochondria, where they serve various functions, including energy production, metabolism and signaling. This import process involves several well-coordinated steps, including recognition, translocation and sorting to different mitochondrial compartments. 1. Synthesis and Recognition of Mitochondrial Targeting Signals The vast majority of mitochondrial proteins are encoded by the nuclear genome. These proteins are synthesized on cytosolic ribosomes and possess a specific targeting sequence known as the mitochondrial targeting signal (MTS), typically found at the N-terminal. This signal is usually a short hydrophobic sequen...

How are the nascent secretory proteins targeted to the ER?

The targeting of nascent secretory proteins to the endoplasmic reticulum (ER) is a highly coordinated and essential process in eukaryotic cells, especially for proteins that are destined to be secreted outside the cell or localized to membranes and organelles of the endomembrane system. This entire process occurs co-translationally, meaning that the protein is directed to the ER while it is still being synthesized by the ribosome. This mechanism follows a specific pathway called the  Signal Hypothesis,  first proposed by Gunter Blobel, which explains how newly forming proteins are recognized and directed to the ER membrane. The process includes five essential steps, which are explained in detail below: 1. Signal Sequence Recognition Nascent secretory proteins contain a special amino acid stretch called the signal peptide or signal sequence at their N-terminal end. This signal sequence is typically 15–30 amino acids long and contains a hydrophobic core that is recognized as the...

How translocation of secretory proteins takes place across the ER membrane?

The translocation of secretory proteins across the endoplasmic reticulum (ER) membrane is a crucial step in the secretory pathway. This process ensures that newly made proteins enter the lumen of the rough ER, where they begin their journey toward secretion or membrane insertion. Secretory proteins are synthesized by ribosomes in the  cytosol.  However, those meant to enter the ER begin their synthesis with a special short sequence of amino acids called a signal peptide at their  N-terminal end.  This signal peptide acts as a tag, directing the ribosome to the ER. As soon as the signal peptide emerges from the ribosome, it is recognized by a complex known as the  Signal Recognition Particle (SRP).  The SRP binds to the ribosome and signal peptide, temporarily pausing protein synthesis. This pause is necessary to guide the ribosome to the ER membrane without the protein being fully synthesized in the cytosol. The SRP-ribosome complex then docks on the ER mem...

Explain with the help of schematic diagram, protein-sorting pathways in eukaryotic cells

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Protein sorting in eukaryotic cells is the highly regulated process through which newly synthesized proteins are directed to their correct destinations within or outside the cell. It is crucial for maintaining cellular structure, function and homeostasis. This process ensures that enzymes, structural proteins and signaling molecules reach their functional compartments such as the nucleus, mitochondria, endoplasmic reticulum (ER), lysosomes, plasma membrane, or extracellular space. The sorting mechanism relies on signal sequences in the proteins, cellular recognition systems and various sorting pathways. These pathways are crucial for maintaining cellular compartmentalization and function. There are two major types of protein-sorting pathways in eukaryotic cells: Co-translational targeting to the endoplasmic reticulum (ER) Post-translational targeting to other organelles like the nucleus, mitochondria and peroxisomes. 1. Co-translational Sorting Pathway (ER-Dependent Pathway) In this pa...

Desoribe endocytosis of LDL by the cell

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Low-Density Lipoprotein (LDL) is the primary transporter of cholesterol in the bloodstream. Cells acquire cholesterol from LDL particles through a highly specific process called  receptor-mediated endocytosis,  which is a classic example of clathrin-dependent endocytosis. This process begins when LDL particles bind to LDL receptors (LDLR) located on the  plasma membrane.  These receptors are transmembrane glycoproteins that specifically recognize apolipoprotein B-100 (ApoB-100) on the surface of LDL. The receptor-ligand complexes cluster in membrane regions called  clathrin-coated pits.  These regions are lined by the protein clathrin, which forms a polygonal lattice that shapes the invaginated membrane into a vesicle. As the clathrin-coated pit deepens, the membrane undergoes scission with the help of dynamin, a GTPase that pinches off the vesicle from the plasma membrane. This forms a clathrin-coated vesicle containing the LDL-receptor complexes. The clat...

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Which neurological disorders are linked to increase dopamine secretion?