NEET-PG 2012 Practice Questions

Q: Skeletal derivative of 2nd pharyngeal arch -

Stapes. ***Stapes*** - The **2nd pharyngeal arch** (also known as the hyoid arch) gives rise to several structures, including Reichert's cartilage, which forms the **stapes** bone, the styloid process, the lesser horn of the hyoid, and the upper part of the hyoid body. - Its muscles include the **stapedius**, stylohyoid, posterior belly of the digastric, and muscles of facial expression. *Malleus* - The **malleus** is derived from the **1st pharyngeal arch** (Meckel's cartilage), along with the incus. - The 1st pharyngeal arch is also responsible for forming the malleus, incus, and mandible. *Incus* - Similar to the malleus, the **incus** also originates from the **1st pharyngeal arch** (Meckel's cartilage). - Both the malleus and incus are crucial components of the middle ear ossicles but are structurally distinct from the stapes. *Maxilla* - The **maxilla** development is primarily from the **maxillary prominence** of the first pharyngeal arch, which is a subdivision of the first arch but does not originate from the 2nd arch. - It forms a significant portion of the midface and upper jaw, contributing to the nasal cavity and orbital floor.

Q: What is the outer layer of the blastocyst called?

Trophoblast. ***Trophoblast*** - The **trophoblast** is the outer layer of cells of the blastocyst, which goes on to form the **placenta** and other extraembryonic tissues [1]. - It plays a crucial role in the **implantation** of the blastocyst into the uterine wall and in producing hormones [1]. *Primitive streak* - The **primitive streak** is a structure that forms during **gastrulation**, much later than the initial blastocyst stage. - It establishes the **anterior-posterior axis** and initiates the formation of the three germ layers. *Yolk sac* - The **yolk sac** is an extraembryonic membrane that forms within the blastocyst cavity, but it is not the outermost layer of the entire structure. - It is involved in early **nutrient transfer** and **blood cell formation** before the placenta is fully functional. *Embryo proper* - The **embryo proper**, derived from the **inner cell mass (ICM)**, is the part of the blastocyst that will develop into the actual embryo [2]. - It is located *inside* the trophoblast layer, not forming the outer boundary of the blastocyst [2].

Q: Which of the following is a tributary of the coronary sinus?

Great cardiac vein. ***Great cardiac vein*** - The **great cardiac vein** is a major tributary that drains into the **coronary sinus**, carrying deoxygenated blood from the anterior and left ventricular walls [1]. - It travels alongside the **anterior interventricular artery** (LAD) and then wraps around the left side of the heart to join the coronary sinus [1]. *Anterior cardiac vein* - The **anterior cardiac veins** typically collect blood directly into the **right atrium**, bypassing the coronary sinus [1]. - They primarily drain the anterior wall of the right ventricle. *Thebesian vein* - **Thebesian veins** (or venae cordis minimae) are small veins that drain blood from the **myocardium directly into the heart chambers**, predominantly the atria [1]. - They represent a direct communication between the myocardial capillaries and the heart chambers, not tributaries of the coronary sinus. *Smallest cardiac vein* - The term "smallest cardiac vein" is often used synonymously with **Thebesian veins** [1]. - These veins empty directly into the **heart chambers**, serving as an ancillary drainage system, rather than converging into the coronary sinus.

Q: Waldeyer's fascia lies?

Behind the rectum.. ***Behind the rectum*** - **Waldeyer’s fascia**, also known as the **sacrorectal fascia**, is a retrorectal connective tissue sheet located between the **rectum** and the **sacrum**. - It plays a crucial role in supporting the rectum and forms part of the posterior rectosacral space, separating the rectum from the sacral bone and nerves. *In front of the bladder* - The space in front of the bladder is typically referred to as the **retropubic space of Retzius**, containing loose connective tissue and fat. - No specific fascial layer named Waldeyer's fascia is located in this anterior position relative to the bladder. *Between the bladder and uterus* - This space, known as the **vesicouterine pouch** or **anterior cul-de-sac**, is a peritoneal reflection between the bladder and the uterus [1]. - It does not contain a structure known as Waldeyer's fascia. *Between the uterus and rectum* - This space is the **rectouterine pouch** or **Pouch of Douglas**, which is the deepest part of the peritoneal cavity in females [2]. - While important surgically, it does not correspond to the location of Waldeyer's fascia.

Q: In the electron transport chain (ETC), which enzyme does cyanide inhibit?

Cytochrome c oxidase (Complex IV). ***Cytochrome c oxidase (Complex IV)*** - Cyanide binds to the **ferric iron (Fe3+)** in the heme a3 component of cytochrome c oxidase, blocking the final transfer of electrons to oxygen. - This inhibition effectively halts the entire **electron transport chain** and **oxidative phosphorylation**, leading to rapid cellular energy depletion. *Complex I (NADH dehydrogenase)* - While other toxins can inhibit Complex I (e.g., rotenone, amytal), **cyanide specifically targets Complex IV**. - Inhibition here prevents the entry of electrons from **NADH** into the ETC, but it's not cyanide's primary site of action. *Complex III (Cytochrome bc1 complex)* - Complex III is involved in transferring electrons from **ubiquinol** to cytochrome c, but it is not directly inhibited by cyanide. - Antimycin A is a well-known inhibitor of Complex III. *Complex II (Succinate dehydrogenase)* - Complex II directly receives electrons from **succinate** in the citric acid cycle and passes them to ubiquinone, bypassing Complex I. - Cyanide does not inhibit Complex II; inhibitors of this complex include malonate.

Q: What cofactor is required for the proper functioning of glucose-6-phosphate dehydrogenase?

NADP. ***NADP*** - **NADP+** (nicotinamide adenine dinucleotide phosphate) acts as the **electron acceptor** in the **glucose-6-phosphate dehydrogenase (G6PD)** reaction, becoming **NADPH**. - **NADPH** is crucial for maintaining the **redox balance** in cells, particularly in red blood cells, by reducing **oxidative stress**. *NAD* - **NAD+** (nicotinamide adenine dinucleotide) is a primary cofactor for many **dehydrogenase reactions** in catabolic pathways like **glycolysis** and the **Krebs cycle**. - It primarily functions as an electron acceptor in pathways that generate **ATP**, distinct from the role of **NADPH** in reductive biosynthesis and antioxidant defense. *FAD* - **FAD** (flavin adenine dinucleotide) is a coenzyme derived from **riboflavin (vitamin B2)** that is involved in various redox reactions, often in the form of **flavoproteins**. - Enzymes like **succinate dehydrogenase** in the electron transport chain utilize **FAD** as an electron acceptor, which is not the case for G6PD. *FMN* - **FMN** (flavin mononucleotide) is another coenzyme derived from **riboflavin**, structurally similar to FAD but lacking the additional adenosine monophosphate. - It participates in electron transfer reactions, particularly within **complex I** of the **electron transport chain**, but is not a cofactor for G6PD.

Q: Enzyme causing covalent bond cleavage without hydrolysis ?

Lyase. ***Lyase*** - **Lyases** are enzymes that catalyze the cleavage of **covalent bonds** (C-C, C-O, C-N, and others) by means other than hydrolysis or oxidation, often creating a new double bond or a ring structure. - They remove groups from substrates to form double bonds, or conversely, add groups to double bonds. - **Examples:** Aldolase (cleaves C-C bonds in glycolysis), carbonic anhydrase (reversible cleavage of C-O bond), fumarase (C-C bond cleavage in TCA cycle). *Ligase* - **Ligases** are enzymes that join two large molecules by forming a new chemical bond, usually accompanied by the **hydrolysis of ATP**. - They are involved in synthesis reactions, not the cleavage of bonds. *Hydrolase* - **Hydrolases** specifically catalyze the hydrolysis of a chemical bond, involving the **addition of water** across the bond. - They break down large molecules into smaller ones using water - this is the key difference from lyases. *Transferase* - **Transferases** catalyze the transfer of a **functional group** from one molecule (the donor) to another (the acceptor). - They do not cause covalent bond cleavage without hydrolysis but rather move existing groups between molecules.

Q: How do enzymes function in biochemical reactions?

Decrease in activation energy. ***Decrease in activation energy*** - Enzymes act as **biological catalysts** by providing an alternative reaction pathway with a lower **transition state energy**. - This reduction in the **activation energy** allows a higher proportion of reactant molecules to overcome the energy barrier and react, thereby increasing the reaction rate. *Increase in activation energy* - This statement is incorrect as increasing activation energy would slow down the reaction rate, which is contrary to the function of enzymes. - Enzymes are designed to accelerate reactions, not inhibit them, by making them energetically more favorable to proceed. *Shift equilibrium constant* - Enzymes catalyze both the forward and reverse reactions equally, meaning they accelerate the rate at which equilibrium is reached but **do not alter the equilibrium constant (Keq)** of a reaction. - The equilibrium constant is determined by the difference in free energy between reactants and products, which enzymes do not change. *Provide energy to the reaction* - This statement is incorrect because enzymes do **not provide energy** to reactions; they only lower the activation energy barrier. - Enzymes facilitate reactions by stabilizing the transition state, not by adding energy to the system, which would violate thermodynamic principles.

Q: Which of the following is the most characteristic symptom of obstruction of the inferior vena cava?

Paraumblical dilatation. ***Paraumbilical dilatation*** - Obstruction of the **inferior vena cava (IVC)** leads to collateral circulation through superficial veins, especially around the umbilicus, causing **paraumbilical dilatation** (caput medusae). - This collateral flow bypasses the obstructed IVC to return blood to the superior vena cava system. *Thoraco-epigastric dilatation* - This pattern of collateral circulation is more characteristic of **superior vena cava (SVC) obstruction**, where blood from the upper body needs to bypass the SVC. - The dilated veins would typically be seen on the chest and upper abdomen, draining towards the femoral veins. *Oesophageal varices* - **Oesophageal varices** are typically caused by **portal hypertension** [1], often secondary to liver cirrhosis, not directly by IVC obstruction. - They represent portosystemic collateral veins, diverging from the portal system to the systemic circulation [1]. *Haemorrhoids* - **Haemorrhoids** are dilated veins in the anal canal, most commonly caused by **straining** during defecation or conditions that increase intra-abdominal pressure [2]. - While they can be a sign of portal hypertension [1], **IVC obstruction** is not their primary or most characteristic cause.

Q: What is the fixed length of a myosin filament?

1.6 micrometers. ***1.6 micrometers*** - Myosin filaments, also known as **thick filaments**, are integral components of muscle contraction and have a characteristic fixed length. This length is precisely **1.6 micrometers** in mammalian skeletal muscle. - This consistent length is crucial for the **sliding filament model** of muscle contraction, ensuring proper overlap with actin filaments and efficient force generation. *0.16 nm* - This value is significantly too small; **nanometers (nm)** are typically used for atomic or molecular distances, not for entire protein filaments like myosin. - A myosin filament is composed of hundreds of myosin molecules, making its overall length much larger than a fraction of a nanometer. *16 nm* - While nanometers are used for molecular structures, 16 nm is still too small for a myosin filament. The entire filament is roughly **100 times larger** than this value. - This dimension might be more appropriate for the diameter of a single myosin molecule's head region, but not the entire filament's length. *1.6 mm* - This value is significantly too large; **millimeters (mm)** are visible to the naked eye and represent macroscopic objects. - Muscle filaments are microscopic structures, and a length of 1.6 mm would imply they are many times longer than an entire muscle cell.

Question 1

Skeletal derivative of 2nd pharyngeal arch -

Accepted Answer

Stapes

Answer

Malleus

Answer

Incus

Answer

Maxilla

Question 2

What is the outer layer of the blastocyst called?

Accepted Answer

Trophoblast

Answer

Embryo proper

Answer

Primitive streak

Answer

Yolk sac

Question 3

Which of the following is a tributary of the coronary sinus?

Accepted Answer

Great cardiac vein

Answer

Anterior cardiac vein

Answer

Smallest cardiac vein

Answer

Thebesian vein

Question 4

Waldeyer's fascia lies?

Accepted Answer

Behind the rectum.

Answer

In front of the bladder.

Answer

Between the bladder and uterus.

Answer

Between the uterus and rectum.

Question 5

In the electron transport chain (ETC), which enzyme does cyanide inhibit?

Accepted Answer

Cytochrome c oxidase (Complex IV)

Answer

Complex II (Succinate dehydrogenase)

Answer

Complex I (NADH dehydrogenase)

Answer

Complex III (Cytochrome bc1 complex)

Question 6

What cofactor is required for the proper functioning of glucose-6-phosphate dehydrogenase?

Accepted Answer

NADP

Answer

NAD

Answer

FAD

Answer

FMN

Question 7

Enzyme causing covalent bond cleavage without hydrolysis ?

Accepted Answer

Lyase

Answer

Ligase

Answer

Hydrolase

Answer

Transferase

Question 8

How do enzymes function in biochemical reactions?

Accepted Answer

Decrease in activation energy

Answer

Increase in activation energy

Answer

Shift equilibrium constant

Answer

Provide energy to the reaction

Question 9

Which of the following is the most characteristic symptom of obstruction of the inferior vena cava?

Accepted Answer

Paraumblical dilatation

Answer

Thoraco-epigastric dilatation

Answer

Haemorrhoides

Answer

Oesophageal varices

Question 10

What is the fixed length of a myosin filament?

Accepted Answer

1.6 micrometers

Answer

0.16 nm

Answer

16 nm

Answer

1.6 mm

NEET-PG 2012

Anatomy

Biochemistry

Internal Medicine

Physiology