NEET-PG 2012 Practice Questions

Q: Which of the following cell types is neuroectodermal in origin?

Smooth muscle cells. ***Smooth muscle cells*** - This is the **correct answer** based on a **specific exception**: smooth muscle cells of the **iris dilator and sphincter muscles** and the **ciliary muscle** in the eye are derived from **neuroectoderm** (specifically from the **optic cup**, an outgrowth of the neural tube). - **Important note:** The vast majority of smooth muscle in the body is of **mesodermal origin** (e.g., in blood vessels, GI tract, respiratory tract). This question tests knowledge of this **notable embryological exception**. - In the context of the given options, this is the only cell type with any neuroectodermal component. *Skeletal muscle cells* - Skeletal muscle cells are entirely derived from the **paraxial mesoderm**, specifically from **somites** (myotome portion). - They form the voluntary muscles of the body and are **never** of neuroectodermal origin. *Endothelial cells* - Endothelial cells lining blood vessels and lymphatic vessels are derived from the **mesoderm** (specifically from **angioblasts**). - They are part of the cardiovascular system and are **entirely mesodermal** in origin. *Cardiac muscle cells* - Cardiac muscle cells are derived from the **splanchnic mesoderm** (lateral plate mesoderm). - The heart musculature is **entirely mesodermal** with no neuroectodermal contribution. **Clinical Pearl:** Classic neuroectodermal derivatives include neurons, glial cells (astrocytes, oligodendrocytes), ependymal cells, and neural crest derivatives (Schwann cells, melanocytes, chromaffin cells). The smooth muscle of the iris represents an important exception to the general rule that smooth muscle is mesodermal.

Q: What is the preferred site for intramuscular injection in the gluteus muscle?

Superolateral. ***Superolateral*** - This quadrant is preferred because it avoids the **sciatic nerve** and major **blood vessels**, minimizing the risk of injury. - The muscle mass in this region, primarily the **gluteus medius**, is sufficient for medication absorption. *Inferomedial* - This area carries a high risk of damaging the **sciatic nerve**, which runs through the lower, medial part of the gluteus. - Injecting here can also hit major **blood vessels**, leading to bleeding or hematoma. *Superomedial* - While somewhat safer than the inferomedial quadrant, this area is still closer to the **sciatic nerve** exit point and major vessels compared to the superolateral region. - The muscle bulk is also less prominent here compared to the superolateral aspect. *Inferolateral* - This quadrant is still in the vicinity of the **sciatic nerve** and major blood vessels, making it riskier than the superolateral site. - There is less muscle mass here compared to the superior quadrants, which can lead to improper drug absorption.

Q: Which of the following is true about coeliac plexus block?

Most common side effects include diarrhea and hypotension. ***Most common side effects include diarrhea and hypotension*** - A coeliac plexus block interrupts **sympathetic innervation** to the upper abdominal organs, which can lead to parasympathetic dominance. - This imbalance often results in **increased gastrointestinal motility (diarrhea)** and **vasodilation (hypotension)** as common side effects. *Located retroperitoneally at the level of L3* - The coeliac plexus is typically located **retroperitoneally** at the level of the **T12-L1 vertebrae**, not L3. - Its position is generally superior to the renal arteries, which are closer to L1-L2. *Usually done unilaterally* - A coeliac plexus block is almost always performed **bilaterally** or with a single posterior approach aiming for bilateral spread to effectively block the plexus. - The coeliac plexus is an extensive network, and a unilateral block would likely provide inadequate pain relief. *Useful for painful conditions of the lower abdomen* - The coeliac plexus primarily innervates **upper abdominal organs** (e.g., pancreas, liver, stomach, small intestine, kidneys, adrenal glands). - It is therefore generally **ineffective for lower abdominal pain**, which is innervated by different sympathetic plexuses (e.g., superior and inferior hypogastric plexuses).

Q: What are isoenzymes?

Physically distinct forms of the same enzyme. ***Physically distinct forms of the same enzyme*** - Isoenzymes are **multiple forms of an enzyme** that catalyze the **same reaction** but differ in their **physical or biochemical properties**, such as electrophoretic mobility, optimal pH, or kinetic parameters. - These differences usually arise from **genetic variations** (different genes encoding isoforms) or **post-translational modifications** (e.g., phosphorylation, glycosylation). *Physically same forms of different enzymes* - This statement is incorrect as isoenzymes are forms of the **same enzyme**, not different enzymes. - While different enzymes can catalyze similar reactions in certain pathways, they are not referred to as isoenzymes if they are structurally identical. *Forms of same enzyme that catalyze different reactions* - This describes enzymes with **broad substrate specificity** or those that act on different substrates but are not necessarily isoenzymes. - Isoenzymes specifically catalyze the **same chemical reaction**, but they may do so with different efficiencies or under different regulatory controls. *Forms of different enzyme that catalyze same reactions* - This describes a scenario where different enzymes might exhibit **catalytic promiscuity** or broad specificity, but not isoenzymes. - Isoenzymes are always derived from the **same parent enzyme** and catalyze the identical reaction.

Q: The thickness of the endometrium at the time of implantation is:

7 - 10 mm. ***7 - 10 mm*** - At the time of **implantation** (day 6-10 post-fertilization, around day 20-24 of the menstrual cycle), the endometrium is in the **mid-secretory phase** and measures **7-10 mm** in thickness. - This is the **optimal thickness** for successful embryo implantation, characterized by a receptive endometrium with **decidualization**, **spiral artery development**, and **glycogen-rich glandular secretions**. - Endometrial thickness <7 mm is associated with **poor implantation rates** and reduced pregnancy success. *3 - 4 mm* - An endometrial thickness of 3-4 mm is **too thin** for successful implantation. - This thickness is typically seen in the **early proliferative phase** (immediately after menstruation), not during the implantation window. - Thin endometrium (<7 mm) is associated with **poor receptivity** and lower pregnancy rates in both natural conception and assisted reproduction. *20 - 30 mm* - An endometrial thickness of 20-30 mm is **abnormally thick** and not conducive to normal implantation. - Such thickness may indicate **endometrial hyperplasia**, **polyps**, or other pathological conditions requiring investigation. *30 - 40 mm* - An endometrial thickness of 30-40 mm is **severely abnormal** and would likely prevent successful implantation. - This extreme thickness suggests significant pathology such as **endometrial hyperplasia** or **malignancy** and requires urgent evaluation.

Q: Nonshivering thermogenesis in adults is due to:

Brown fat between the shoulders. ***Brown fat between the shoulders*** - In adults, the primary **effector tissue** for **non-shivering thermogenesis** is **brown adipose tissue (BAT)**, with major depots located between the shoulders, around the neck, and along the spine. - **BAT** contains specialized mitochondria with **uncoupling protein 1 (UCP1)** that uncouples oxidative phosphorylation, generating heat instead of ATP. - This is the tissue where non-shivering thermogenesis actually occurs, making it the direct answer to what non-shivering thermogenesis is "due to." *Noradrenaline* - **Noradrenaline** is the key neurotransmitter that **activates brown fat** via **β3-adrenergic receptors** to initiate non-shivering thermogenesis. - While noradrenaline is the **trigger/stimulus**, the actual heat production occurs in brown adipose tissue. - Noradrenaline itself does not produce heat directly; it acts as the signal that activates the thermogenic machinery in BAT. *Thyroid hormone* - **Thyroid hormone** increases **basal metabolic rate** and can potentiate the thermogenic response by upregulating UCP1 expression in brown fat. - Its role is **permissive and long-term** rather than being the immediate effector of acute non-shivering thermogenesis. - It modulates overall cellular metabolism but is not the primary mechanism for rapid heat generation in cold exposure. *Muscle metabolism* - **Muscle contraction** during shivering generates heat through increased ATP hydrolysis, which is **shivering thermogenesis**. - **Non-shivering thermogenesis** specifically refers to heat production **without muscle contraction**, making muscle metabolism the mechanism for shivering, not non-shivering, thermogenesis.

Q: Which of the following is NOT a location where multi-unit smooth muscle is present?

Gut. ***Gut*** - The gut primarily contains **unitary (single-unit) smooth muscle**, characterized by cells connected by **gap junctions** that allow for synchronized contractions (e.g., peristalsis). - This type of smooth muscle exhibits **spontaneous rhythmic contractions** due to pacemaker cells, and its activity is modulated by neural and hormonal inputs rather than requiring individual innervation of each cell. - Multi-unit smooth muscle is **NOT present** in the gut. *Blood vessels* - Many larger blood vessels (e.g., large arteries) contain **multi-unit smooth muscle**, which allows for **fine, graded control** over vascular tone and blood flow. - Each muscle cell is typically **innervated individually**, enabling precise regulation of contraction strength. *Iris* - The iris contains **multi-unit smooth muscle** (e.g., sphincter pupillae and dilator pupillae muscles) which control pupil size. - These muscles require **individual innervation** to allow for very fine and precise movements in response to light intensity changes. *Ciliary muscle* - The ciliary muscle of the eye contains **multi-unit smooth muscle**, which controls the shape of the lens for accommodation (focusing). - These muscle fibers are **individually innervated** to allow precise control of lens curvature for near and far vision.

Q: From the given pressure-volume curve, identify the end-diastolic volume (EDV) and end-systolic volume (ESV), then calculate the ejection fraction using the formula EF = (EDV - ESV)/EDV × 100%.

60%. ***60%*** - From the pressure-volume loop, the **end-diastolic volume (EDV)** is the volume at point 'a', which is **130 mL**. - The **end-systolic volume (ESV)** is the volume at point 'd', which is **50 mL**. - Using the formula EF = (EDV - ESV) / EDV × 100% = (130 mL - 50 mL) / 130 mL × 100% = 80 mL / 130 mL × 100% = **61.5%**, which rounds to **60%** (the closest option). *40%* - To obtain an ejection fraction of 40%, the ESV would need to be higher, or the EDV lower, than what is indicated by the points 'a' and 'd' on the graph. - (130 - ESV) / 130 = 0.40 => 130 - ESV = 52 => ESV = 78 mL. This isn't consistent with the graph. *50%* - An ejection fraction of 50% would mean that the heart ejected half of its EDV. - (130 - ESV) / 130 = 0.50 => 130 - ESV = 65 => ESV = 65 mL. This value for ESV is not depicted at point 'd'. *55%* - For an ejection fraction of 55%, the calculation would yield a different ESV than what is presented in the curve. - (130 - ESV) / 130 = 0.55 => 130 - ESV = 71.5 => ESV = 58.5 mL. This is not the ESV at point 'd'.

Q: What happens to the pressure in the calf compartment during the heel touch phase of walking?

Increases compared to resting pressure. ***Increases compared to resting pressure*** - During **heel strike (initial contact)**, the calf muscles (**gastrocnemius and soleus**) contract eccentrically to control ankle dorsiflexion and decelerate the foot - Simultaneous **weight bearing** and **muscle contraction** within the confined fascial compartment lead to increased intramuscular pressure - This is a well-documented phenomenon in gait biomechanics and exercise physiology *Decreases compared to resting pressure* - Incorrect: Muscle activation and weight bearing during initial contact inherently increase compartment pressure - Pressure decrease occurs during swing phase when the limb is unloaded and muscles are relaxed *First increases and then decreases* - While pressure varies throughout the complete gait cycle, the **heel touch phase specifically** is characterized by an initial pressure increase - The brief duration of heel strike does not typically show a biphasic pressure pattern within this single phase *Remains the same as resting pressure* - Incorrect: Active weight bearing and eccentric muscle contraction during heel strike necessarily elevate intramuscular pressure above resting levels - Resting pressure only occurs when the limb is unloaded and muscles are inactive

Q: Haploid number of chromosomes is first seen in?

Secondary spermatocyte. ***Secondary spermatocyte*** - A secondary spermatocyte is formed after **meiosis I**, where the homologous chromosomes are separated, resulting in a cell with a **haploid number of chromosomes (n)**, although each chromosome still consists of two sister chromatids. - This is the **first stage** where haploidy is achieved in spermatogenesis. - These cells are transient and quickly undergo meiosis II to form spermatids. *Spermatogonia* - Spermatogonia are **diploid (2n)** germline stem cells that undergo mitosis to produce more spermatogonia or differentiate into primary spermatocytes. - They contain the full complement of chromosomes found in somatic cells. *Primary spermatocytes* - Primary spermatocytes are also **diploid (2n)** cells that enter meiosis I. - Before meiosis I, DNA replication occurs, so each chromosome consists of two sister chromatids, but the cell still maintains a diploid chromosome number. *Spermatids* - Spermatids are formed after **meiosis II** from secondary spermatocytes and are also **haploid (n)**. - However, secondary spermatocytes become haploid **earlier** in the process, immediately following the reductional division of meiosis I.

Question 1

Which of the following cell types is neuroectodermal in origin?

Accepted Answer

Smooth muscle cells

Answer

Skeletal muscle cells

Answer

Endothelial cells

Answer

Cardiac muscle cells

Question 2

What is the preferred site for intramuscular injection in the gluteus muscle?

Accepted Answer

Superolateral

Answer

Inferolateral

Answer

Superomedial

Answer

Inferomedial

Question 3

Which of the following is true about coeliac plexus block?

Accepted Answer

Most common side effects include diarrhea and hypotension

Answer

Usually done unilaterally

Answer

Located retroperitoneally at the level of L3

Answer

Useful for painful conditions of the lower abdomen

Question 4

What are isoenzymes?

Accepted Answer

Physically distinct forms of the same enzyme

Answer

Physically same forms of different enzymes

Answer

Forms of same enzyme that catalyze different reactions

Answer

Forms of different enzyme that catalyze same reactions

Question 5

The thickness of the endometrium at the time of implantation is:

Accepted Answer

7 - 10 mm

Answer

20 - 30 mm

Answer

30 - 40 mm

Answer

3 - 4 mm

Question 6

Nonshivering thermogenesis in adults is due to:

Accepted Answer

Brown fat between the shoulders

Answer

Muscle metabolism

Answer

Thyroid hormone

Answer

Noradrenaline

Question 7

Which of the following is NOT a location where multi-unit smooth muscle is present?

Accepted Answer

Gut

Answer

Blood vessels

Answer

Iris

Answer

Ciliary muscle

Question 8

From the given pressure-volume curve, identify the end-diastolic volume (EDV) and end-systolic volume (ESV), then calculate the ejection fraction using the formula EF = (EDV - ESV)/EDV × 100%.

Accepted Answer

60%

Answer

40%

Answer

50%

Answer

55%

Question 9

What happens to the pressure in the calf compartment during the heel touch phase of walking?

Accepted Answer

Increases compared to resting pressure

Answer

Decreases compared to resting pressure

Answer

First increases and then decreases

Answer

Remains the same as resting pressure

Question 10

Haploid number of chromosomes is first seen in?

Accepted Answer

Secondary spermatocyte

Answer

Spermatogonia

Answer

Primary spermatocytes

Answer

Spermatids

NEET-PG 2012

Anatomy

Anesthesiology

Biochemistry

Obstetrics and Gynecology

Physiology