NEET-PG 2013 Practice Questions

Q: Which muscle is not part of the superficial anterior compartment of the forearm?

Flexor pollicis longus (FPL). **Flexor pollicis longus (FPL)** - The **FPL** is located in the **deep anterior compartment** of the forearm, differentiating it from the superficial muscles [1]. - Its primary function is **flexion of the thumb's interphalangeal joint**, requiring a deeper anatomical position for mechanical advantage [1]. *FDS* - The **Flexor digitorum superficialis (FDS)** is a key muscle of the superficial anterior compartment, visible just beneath the skin and fascia. - It is responsible for **flexing the middle phalanges** of the medial four digits. *FCR* - The **Flexor carpi radialis (FCR)** is situated in the superficial anterior compartment, running obliquely across the forearm. - It functions in **flexion and abduction of the wrist**. *Palmaris longus* - The **Palmaris longus** is a superficial anterior compartment muscle, though it is absent in a significant portion of the population. - When present, its main action is **flexion of the wrist** and tightening of the palmar aponeurosis.

Q: What is the main enzyme involved in glycogen breakdown (glycogenolysis)?

Glycogen phosphorylase. ***Glycogen phosphorylase*** - This is the **rate-limiting and primary enzyme** for **glycogenolysis**, the breakdown of glycogen into glucose units. - It cleaves **α-1,4-glycosidic bonds** in glycogen, releasing **glucose-1-phosphate** units. - Regulated by both **allosteric mechanisms** and **hormonal control** (epinephrine, glucagon). - Works until it reaches 4 glucose residues from a branch point, where debranching enzyme takes over. *Glycogen synthase* - This is the main enzyme for **glycogenesis** (glycogen synthesis), not breakdown. - It catalyzes formation of α-1,4-glycosidic bonds to build glycogen chains. - This is the opposite direction of metabolism from what the question asks about. *Glucose-6-phosphatase* - This enzyme is involved in **gluconeogenesis** and the final step of converting **glucose-6-phosphate to free glucose**. - It is NOT directly involved in glycogen breakdown itself, but rather in the subsequent conversion pathway. - Found primarily in **liver and kidney** to release free glucose into blood. *Hexokinase* - This enzyme phosphorylates free glucose to **glucose-6-phosphate** (opposite direction). - It is involved in **glucose utilization**, not glycogen breakdown. - It traps glucose inside cells for metabolism or glycogen synthesis.

Q: Glucagon stimulates

Gluconeogenesis. ***Gluconeogenesis*** - **Glucagon** is a hormone that primarily acts to raise **blood glucose levels** by stimulating the production of glucose from non-carbohydrate sources. - This process, **gluconeogenesis**, occurs mainly in the liver and is initiated by glucagon to counteract hypoglycemia. *Glycogenesis* - **Glycogenesis** is the process of synthesizing **glycogen** from glucose and is primarily stimulated by insulin when blood glucose levels are high. - Glucagon's role is to *inhibit* glycogen synthesis and instead promote glycogen breakdown. *Fatty acid synthesis* - **Fatty acid synthesis** is an anabolic process that primarily occurs when there is an excess of energy and glucose, often stimulated by **insulin**. - Glucagon generally has an **inhibitory effect** on fatty acid synthesis, as its main goal is to mobilize energy stores, not create them. *Glycolysis* - **Glycolysis** is the breakdown of glucose to produce energy, and it is stimulated when glucose is abundant and energy is needed. - Glucagon primarily acts to *inhibit* glycolysis in the liver, thereby conserving glucose for use by other tissues and promoting its release into the bloodstream.

Q: Which of the following amino acids is not involved in the production of creatine?

Alanine. ***Alanine*** - **Alanine** is not directly involved as a precursor for **creatine synthesis**. It can be converted to pyruvate and enter the gluconeogenic pathway. - The primary amino acids involved in **creatine synthesis** are arginine, glycine, and methionine. *Glycine* - **Glycine** is a direct precursor for creatine, reacting with arginine in the first step of its synthesis to form **guanidinoacetate**. - This reaction is catalyzed by **arginine:glycine amidinotransferase (AGAT)**. *Methionine* - **Methionine**, in the form of **S-adenosylmethionine (SAM)**, acts as the methyl donor in the second step of creatine synthesis. - It methylates guanidinoacetate to form **creatine**, a reaction catalyzed by **guanidinoacetate methyltransferase (GAMT)**. *Arginine* - **Arginine** donates its guanidino group to glycine, forming **guanidinoacetate**, the initial intermediate in creatine synthesis. - This is the first committed step in the **creatine biosynthesis pathway**.

Q: Which of the following is NOT a feature of Peutz-Jeghers syndrome?

Autosomal recessive inheritance. ***High risk of malignancy*** - Peutz-Jeghers syndrome is primarily associated with **benign hamartomatous polyps**, not a **high risk of malignancy**, which distinguishes it from other syndromes. - Although patients may develop cancers [1], the syndrome itself does not inherently denote a high malignancy risk like other syndromes such as familial adenomatous polyposis. *Autosomal dominant* - This syndrome is indeed **autosomal dominant**, caused by mutations in the STK11 gene. - Families with this condition typically show **vertical transmission**, characteristic of autosomal dominant inheritance. *Hamartomatous polyp* - Individuals with Peutz-Jeghers syndrome develop **hamartomatous polyps**, which are a hallmark feature of the condition [1]. - These polyps can occur in the gastrointestinal tract and are benign lesions rather than adenomatous type seen in other syndromes [1]. *Mucocutaneous pigmentation* - Mucocutaneous pigmentation, such as **freckling around the lips and buccal mucosa**, is a key clinical feature of Peutz-Jeghers syndrome. - This pigmentation usually appears in childhood and is often a distinguishing sign of the syndrome.

Q: Which is not a feature of paroxysmal nocturnal hemoglobinuria?

Increased LAP score. ***Increased LAP score*** - In paroxysmal nocturnal hemoglobinuria, the **LAP score** is typically **low** due to ineffective hematopoiesis and not elevated. - The presence of a low LAP score is inconsistent with the features of this condition, making it the correct choice. *Thrombosis* - Paroxysmal nocturnal hemoglobinuria is **associated with a high risk of thrombosis**, particularly in the **venous system** [2]. - This is due to **increased platelet activation** and excessive thrombin generation resulting from hemolysis. *Hemolysis* - **Hemolysis** is a hallmark feature of paroxysmal nocturnal hemoglobinuria, where there is **destruction of red blood cells** [2,3]. - Patients often present with signs of hemolytic anemia including **elevated bilirubin** and **low haptoglobin** levels. *Thrombocytopenia* - **Thrombocytopenia** is a common finding in paroxysmal nocturnal hemoglobinuria due to **expanded consumption** of platelets during episodes of hemolysis. - This can lead to an **increased risk of bleeding** in affected patients. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Blood And Bone Marrow Disease, pp. 601-602. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Red Blood Cell and Bleeding Disorders, pp. 650-651.

Q: Which of the following statements is false regarding hereditary spherocytosis?

Decreased MCHC. ***Decreased MCHC*** - Hereditary spherocytosis typically presents with an **increased MCHC** due to the spherocytes being more concentrated. - MCHC is a measure of the hemoglobin concentration in red blood cells, and in spherocytosis, this value is often elevated rather than decreased. *Defect in ankyrin* - This is a true statement; hereditary spherocytosis is associated with a defect in **ankyrin**, a protein that helps maintain the cell's membrane structure [2]. - Mutations in ankyrin lead to instability of the red blood cell membrane, resulting in spherocyte formation [2]. *Decreased MCV* - In hereditary spherocytosis, MCV is often **normal or slightly increased**, as it reflects the volume of red blood cells, which can be misinterpreted due to the presence of spherocytes. - Spherocytes are smaller cells, which can mistakenly suggest a falsely decreased MCV if not properly interpreted [1]. *Reticulocytosis* - This condition typically presents with **reticulocytosis** as a response to hemolysis, indicating the bone marrow is producing more red blood cells to compensate [1]. - The presence of reticulocytosis is a common finding in hereditary spherocytosis due to increased destruction of spherocytes. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Blood And Bone Marrow Disease, pp. 597-598. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Red Blood Cell and Bleeding Disorders, pp. 640-641.

Q: According to WHO/ISN classification, which class of lupus nephritis shows a membranous pattern in SLE?

Membranous pattern. ***Membranous pattern*** - This corresponds to **Class V lupus nephritis** in the WHO/ISN classification, characterized by widespread immune complex deposition along the **glomerular basement membrane (GBM)**. - The subepithelial immune deposits lead to GBM thickening, creating the characteristic membranous pattern on light microscopy. - This pattern resembles idiopathic membranous nephropathy but occurs in the context of SLE. *Mesangial pattern involvement* - This refers to **Class I (minimal mesangial LN)** or **Class II (mesangial proliferative LN)**, where immune deposits are primarily confined to the mesangium. - There is minimal or no involvement of the glomerular capillary walls, distinguishing it from the membranous pattern. *Diffuse proliferative pattern* - This is **Class IV lupus nephritis**, the most severe form characterized by widespread **endocapillary and/or extracapillary proliferation** involving ≥50% of glomeruli. - The primary feature is cellular proliferation (mesangial, endocapillary, epithelial crescents), not the subepithelial immune deposits typical of membranous pattern. *Focal proliferative pattern* - This corresponds to **Class III lupus nephritis**, involving **endocapillary or extracapillary proliferation** in <50% of glomeruli. - Distinguished by focal (not diffuse) involvement and active proliferation rather than the membranous pattern seen in Class V.

Q: Cell bodies of orexigenic neurons are present in?

Lateral hypothalamic area. ***Lateral hypothalamic area*** - The **lateral hypothalamic area** (LHA) contains neurons that produce **orexin (hypocretin)**, a neuropeptide critical for promoting appetite and wakefulness. - Stimulation of the LHA leads to increased food seeking and consumption, earning it the moniker "**feeding center**." *Dorsal raphe* - The **dorsal raphe nucleus** is a key source of **serotonin** in the brain, involved in mood, sleep-wake cycles, and appetite regulation (often promoting satiety). - It does not primarily house orexigenic neurons that directly stimulate appetite. *Locus coerulus* - The **locus coeruleus** is the primary source of **norepinephrine** in the brain, playing a significant role in arousal, attention, and stress response. - While it modulates appetitive behaviors indirectly, its neurons are not the primary orexigenic cell bodies. *Hippocampus* - The **hippocampus** is crucial for **learning, memory formation**, and spatial navigation. - It is not directly involved in the primary neural circuits that control hunger and satiety through orexigenic neuropeptides.

Q: Which type of nerve fibers are responsible for carrying joint position and vibration sense?

A-beta fibers. ***A-beta fibers*** - **A-beta fibers** are **large-diameter, myelinated** sensory fibers that conduct impulses rapidly. - They are primarily responsible for transmitting **light touch, pressure, joint position (proprioception), and vibration sense**. - **This is the correct answer** because A-beta fibers carry **BOTH joint position AND vibration sense together**. *A-alpha fibers* - **A-alpha fibers** are the **largest and fastest** conducting nerve fibers. - They include **motor nerves to skeletal muscles** and **sensory fibers from muscle spindles (Ia) and Golgi tendon organs (Ib)**. - While Ia fibers (A-alpha) do carry **proprioception from muscle spindles**, they do **NOT carry vibration sense**. - The question asks for fibers carrying **BOTH** joint position **AND** vibration sense, making A-beta the correct answer. *C fibers* - **C fibers** are **small-diameter, unmyelinated** nerve fibers with **slow conduction velocities**. - They are responsible for transmitting **dull, aching pain, temperature, and crude touch**. *A-delta fibers* - **A-delta fibers** are **small-diameter, thinly myelinated** nerve fibers with an intermediate conduction velocity. - They primarily transmit **sharp, fast pain** and **cold temperature sensations**.

Question 1

Which muscle is not part of the superficial anterior compartment of the forearm?

Accepted Answer

Flexor pollicis longus (FPL)

Answer

FDS

Answer

FCR

Answer

Palmaris longus

Question 2

What is the main enzyme involved in glycogen breakdown (glycogenolysis)?

Accepted Answer

Glycogen phosphorylase

Answer

Glycogen synthase

Answer

Glucose-6-phosphatase

Answer

Hexokinase

Question 3

Glucagon stimulates

Accepted Answer

Gluconeogenesis

Answer

Glycogenesis

Answer

Fatty acid synthesis

Answer

Glycolysis

Question 4

Which of the following amino acids is not involved in the production of creatine?

Accepted Answer

Alanine

Answer

Glycine

Answer

Methionine

Answer

Arginine

Question 5

Which of the following is NOT a feature of Peutz-Jeghers syndrome?

Accepted Answer

Autosomal recessive inheritance

Answer

Mucocutaneous pigmentation

Answer

Autosomal dominant

Answer

Hamartomatous polyp

Question 6

Which is not a feature of paroxysmal nocturnal hemoglobinuria?

Accepted Answer

Increased LAP score

Answer

Thrombocytopenia

Answer

Hemolysis

Answer

Thrombosis

Question 7

Which of the following statements is false regarding hereditary spherocytosis?

Accepted Answer

Decreased MCHC

Answer

Defect in ankyrin

Answer

Reticulocytosis

Answer

Normal to increased MCV

Question 8

According to WHO/ISN classification, which class of lupus nephritis shows a membranous pattern in SLE?

Accepted Answer

Membranous pattern

Answer

Diffuse proliferative pattern

Answer

Mesangial pattern involvement

Answer

Focal proliferative pattern

Question 9

Cell bodies of orexigenic neurons are present in?

Accepted Answer

Lateral hypothalamic area

Answer

Dorsal raphe

Answer

Locus coeruleus

Answer

Hippocampus

Question 10

Which type of nerve fibers are responsible for carrying joint position and vibration sense?

Accepted Answer

A-beta fibers

Answer

A-alpha fibers

Answer

C fibers

Answer

A-delta fibers

NEET-PG 2013

Anatomy

Biochemistry

Internal Medicine

Pathology

Physiology