NEET-PG 2015 Practice Questions

Q: Which of the following is not a feature of postmortem staining?

Occurs immediately after death. ***Occurs immediately after death*** - **Livor mortis** (postmortem staining/lividity) does NOT occur immediately after death - it typically begins **20-30 minutes** after death and becomes fully developed within **6-12 hours** - This is the correct answer as it represents a feature that is NOT characteristic of postmortem staining - The delay occurs because it takes time for blood to settle in capillaries due to gravity after circulation stops *Common in dependent part* - This IS a hallmark feature of postmortem staining - Gravity causes blood to pool in the **lowest parts of the body** (dependent areas) - Areas of pressure (where body contacts surface) appear pale due to **capillary compression** *Appears uniformly throughout the body* - This is also NOT a feature of postmortem staining (could be considered another correct answer) - Postmortem staining is **localized to dependent areas**, not uniform throughout - The distribution pattern helps determine body position after death in forensic investigations *Margins are sharp* - Postmortem lividity typically has **ill-defined, diffuse margins** rather than sharp borders - The transition between affected and unaffected areas is gradual - However, this is less definitively wrong compared to the timing and uniformity statements

Q: IFN-gamma is produced by

T-cells. ***T-cells*** - **Interferon-gamma (IFN-γ)** is a crucial cytokine primarily produced by **activated T-lymphocytes**, especially **Th1 cells** and **cytotoxic T lymphocytes (CTLs)**. - Natural killer (NK) cells also produce **IFN-γ**, which plays a key role in **antiviral** and **antitumor immunity**, as well as in promoting **Type 1 immune responses**. *Macrophages* - While macrophages are **responsive to IFN-γ** (e.g., becoming activated), they are not the primary producers of this cytokine. - Macrophages primarily produce other cytokines such as **IL-1, IL-6, TNF-alpha**, and **IL-12** in response to infection or inflammation. *Neutrophils* - **Neutrophils** are key phagocytes in the innate immune system and are primarily involved in engulfing and killing pathogens. - They are not known to be a significant source of **IFN-γ** production; their main defensive mechanisms involve **phagocytosis**, **degranulation**, and **NETosis**. *B-cells* - **B-cells** are central to humoral immunity, specializing in **antibody production** and acting as **antigen-presenting cells**. - They generally do not produce **IFN-γ**; instead, their cytokine repertoire includes **IL-10**, **IL-6**, and **lymphotoxin**.

Q: What is the best method for treating methanol poisoning?

Fomepizole. ***Fomepizole*** - **Fomepizole** (Antizol) is a potent inhibitor of **alcohol dehydrogenase**, the enzyme responsible for metabolizing methanol into toxic metabolites like formic acid [1]. - By inhibiting this enzyme, fomepizole prevents the formation of these harmful metabolites, thus halting the progression of methanol toxicity and reducing mortality [1]. - It is the **gold standard** antidote for methanol poisoning. *Calcium gluconate* - **Calcium gluconate** is primarily used to treat **hypocalcemia** and magnesium toxicity. - It has no role in the direct treatment or detoxification of methanol poisoning. *Deferoxamine* - **Deferoxamine** is a **chelating agent** used to treat **iron toxicity** by binding to iron and facilitating its excretion [3]. - It is not effective for methanol poisoning as it does not interact with methanol or its toxic metabolites. *BAL* - **BAL** (British Anti-Lewisite, dimercaprol) is a chelating agent primarily used for poisoning by **heavy metals** such as arsenic, mercury, and gold [2]. - It has no therapeutic role in methanol poisoning, which involves a different toxicological mechanism.

Q: Volume of distribution of a drug is 500 ml and target concentration of drug in blood is 5 g/L. 20% of administered drug is reached to systemic circulation. What will be the loading dose of that drug -

12.5 gm. ***12.5 gm*** - The formula for loading dose (LD) is: LD = (Target Concentration × Volume of Distribution) / Bioavailability. - Given: Target Concentration = 5 g/L, Volume of Distribution = 500 mL = 0.5 L, Bioavailability = 20% = 0.2. - So, LD = (5 g/L × 0.5 L) / 0.2 = 2.5 g / 0.2 = **12.5 g**. *1 gm* - This value would be obtained if the target concentration was 2 g/L with 100% bioavailability, or if the calculation incorrectly handled the volume or bioavailability factor. - It does not account for the specified **bioavailability of 20%** or the given target concentration and volume of distribution. *5 gm* - This result would be obtained if the bioavailability was assumed to be 50% (LD = 2.5 g / 0.5 = 5 g), or if the volume of distribution was incorrectly used in the calculation. - This option does not correctly factor in the **20% bioavailability** of the administered drug. *25 gm* - This value would result from mistakes such as dividing by bioavailability of 10% instead of 20% (LD = 2.5 g / 0.1 = 25 g), or by multiplying bioavailability instead of dividing by it. - This answer significantly **overestimates** the required dose, which could lead to drug toxicity.

Q: Aortic valve closure occurs in which part of cardiac cycle?

Beginning of isovolumetric relaxation. ***Beginning of isovolumetric relaxation*** - Aortic valve closure marks the end of **ventricular systole** and the start of **isovolumetric relaxation**, as blood ceases to be ejected and the ventricle begins to relax while remaining closed. - This event corresponds to the **second heart sound (S2)** and signifies the beginning of a period where ventricular volume remains constant, but pressure drops. *Beginning of isovolumetric contraction* - This phase begins with the closure of the **mitral and tricuspid valves** (first heart sound, S1), as ventricular pressure rises but volume remains constant before ejection. - The aortic valve is still closed at this point, as ventricular pressure is not yet high enough to open it. *Beginning of ventricular ejection* - This phase begins when the **aortic valve opens** as ventricular pressure exceeds aortic pressure, allowing blood to be ejected from the left ventricle. - Aortic valve closure occurs *after* ejection, not at its beginning. *During rapid ventricular filling* - Rapid ventricular filling occurs when the **mitral valve opens** (following isovolumetric relaxation), allowing blood to flow from the atria into the ventricles. - During this phase, the aortic valve is closed, but its closure happened earlier, at the beginning of isovolumetric relaxation.

Q: EPSP is due to?

Sodium ion influx. ***Sodium ion influx*** - An **Excitatory Postsynaptic Potential (EPSP)** is caused primarily by the binding of an **excitatory neurotransmitter** to its receptor, leading to the opening of **ligand-gated ion channels** permeable to sodium (Na+) ions. - The **influx of positively charged sodium ions** into the postsynaptic neuron causes a **depolarization** of the membrane potential, making it more likely to reach the threshold for an action potential. *Potassium ion influx* - **Potassium (K+) influx** is not the primary mechanism for generating an EPSP; instead, **potassium efflux** (movement out of the cell) is typically involved in **repolarization** after an action potential or in generating **Inhibitory Postsynaptic Potentials (IPSPs)**. - The movement of K+ into the cell would make the membrane potential more negative, leading to **hyperpolarization** or preventing depolarization. *Sodium ion efflux* - **Sodium (Na+) efflux** is mediated by the **Na+/K+ pump** and is crucial for maintaining the resting membrane potential, but it does **not directly cause an EPSP**. - Pumping Na+ out of the cell would **hyperpolarize** the cell or oppose depolarization, making an action potential less likely. *Calcium ion influx* - While **calcium (Ca2+) influx** is vital for many neuronal processes, including **neurotransmitter release** from the presynaptic terminal, it is **not the primary ionic basis** for generating an EPSP in the postsynaptic neuron itself. - Significant Ca2+ influx can occur during an **action potential** or lead to intracellular signaling, but it's not the main depolarizing current responsible for an EPSP.

Q: What is the typical pH range of intracellular fluid (ICF) compared to extracellular fluid (ECF)?

Typically around 7.0, slightly less than ECF. ***Typically around 7.0, slightly less than ECF*** - The **intracellular fluid (ICF)** tends to be slightly more acidic due to metabolic processes within cells that produce **acidic byproducts**. - This makes its pH typically around **7.0–7.2**, which is subtly lower than the extracellular fluid. *Typically around 7.4, slightly more than ICF* - A pH of approximately **7.4** is characteristic of **extracellular fluid (ECF)**, which includes plasma and interstitial fluid. - The ECF is maintained within a **narrow, slightly alkaline** range to support cellular function and enzyme activity throughout the body. *Approximately equal to ECF* - While both fluid compartments are maintained within a **narrow physiological range**, their pH values are not exactly equal. - This slight difference is essential for various biological processes, including maintaining **membrane potential** and **enzyme efficiency**. *Significantly higher than ECF* - The ICF pH is **not significantly higher** than ECF; in fact, it is slightly lower. - Maintaining too high a pH intracellularly would disrupt **cellular metabolism** and **protein structure**.

Question 1

What is a key similarity between the processes of replication and transcription?

Accepted Answer

Involve phosphodiester bond formation with elongation occurring in the 5' - 3' direction.

Answer

Use RNA primers for initiation.

Answer

Use ribonucleotides as precursors.

Answer

Are semi-conservative events.

Question 2

Which of the following is not a feature of postmortem staining?

Accepted Answer

Occurs immediately after death

Answer

Common in dependent part

Answer

Appears uniformly throughout the body

Answer

Margins are sharp

Question 3

IFN-gamma is produced by

Accepted Answer

T-cells

Answer

Macrophages

Answer

Neutrophils

Answer

B-cells

Question 4

Which of the following is a chromosomal instability syndrome?

Accepted Answer

Bloom syndrome

Answer

Fanconi anemia

Answer

Ataxia-telangiectasia

Answer

None of the options

Question 5

What is the best method for treating methanol poisoning?

Accepted Answer

Fomepizole

Answer

Calcium gluconate

Answer

BAL

Answer

Deferoxamine

Question 6

Volume of distribution of a drug is 500 ml and target concentration of drug in blood is 5 g/L. 20% of administered drug is reached to systemic circulation. What will be the loading dose of that drug -

Accepted Answer

12.5 gm

Answer

1 gm

Answer

5 gm

Answer

25 gm

Question 7

Which of the following statements best describes the underlying mechanism of heparin-induced thrombocytopenia?

Accepted Answer

Antibodies are formed against heparin-platelet factor 4 complexes.

Answer

Low molecular weight heparin can also cause heparin-induced thrombocytopenia.

Answer

Vitamin K is not an antidote for heparin-induced thrombocytopenia.

Answer

Heparin-induced thrombocytopenia can occur after several days of heparin therapy.

Question 8

Aortic valve closure occurs in which part of cardiac cycle?

Accepted Answer

Beginning of isovolumetric relaxation

Answer

Beginning of isovolumetric contraction

Answer

During rapid ventricular filling

Answer

Beginning of ventricular ejection

Question 9

EPSP is due to?

Accepted Answer

Sodium ion influx

Answer

Potassium ion influx

Answer

Sodium ion efflux

Answer

Calcium ion influx

Question 10

What is the typical pH range of intracellular fluid (ICF) compared to extracellular fluid (ECF)?

Accepted Answer

Typically around 7.0, slightly less than ECF

Answer

Typically around 7.4, slightly more than ICF

Answer

Approximately equal to ECF

Answer

Significantly higher than ECF

NEET-PG 2015

Biochemistry

Forensic Medicine

Microbiology

Pathology

Pharmacology

Physiology