NEET-PG 2015 Practice Questions

Q: Coenzyme for phenylalanine hydroxylase is?

Tetrahydrobiopterin. ***Tetrahydrobiopterin*** - **Tetrahydrobiopterin (BH4)** is an essential coenzyme for aromatic amino acid hydroxylases, including **phenylalanine hydroxylase (PAH)**. - PAH converts **phenylalanine** to **tyrosine**, and deficiencies in BH4 or PAH itself lead to *phenylketonuria (PKU)*. *Tetrahydrofolate* - **Tetrahydrofolate (THF)** is a coenzyme derived from **folic acid** and is primarily involved in **one-carbon metabolism**, including **purine** and **pyrimidine synthesis**, and various amino acid interconversions. - It does not directly act as a coenzyme for phenylalanine hydroxylase. *Pyridoxal phosphate* - **Pyridoxal phosphate (PLP)**, a derivative of **vitamin B6**, is a crucial coenzyme for many enzymes involved in **amino acid metabolism**, particularly in **transamination**, **decarboxylation**, and side-chain cleavage reactions. - It is not the coenzyme for phenylalanine hydroxylase. *S-adenosyl methionine* - **S-adenosyl methionine (SAM)** is a major **methyl donor** in various biochemical reactions, important for the synthesis of **neurotransmitters**, **hormones**, and **phospholipids**. - While essential for many metabolic pathways, it is not involved as a coenzyme for phenylalanine hydroxylase.

Q: What type of evidence is a dying declaration?

Oral evidence. ***Oral evidence*** - A **dying declaration** is classified as **oral evidence** in Indian law and forensic medicine practice. - It is a **verbal statement** made by a person who is dying, concerning the cause or circumstances of their death, which is later testified to in court by the person who heard it. - Under **Section 32 of the Indian Evidence Act, 1872**, dying declarations are admissible and form substantive evidence. - Though oral in nature, they carry significant evidentiary value and can be the sole basis for conviction if found reliable. *Hearsay evidence* - While technically a dying declaration originates as an **out-of-court statement**, in Indian legal practice it is treated as an **exception to the hearsay rule** and elevated to substantive evidence. - In forensic medicine classification for Indian exams, it is primarily categorized as **oral evidence** rather than hearsay. *Circumstantial evidence* - **Circumstantial evidence** relies on inference to establish a fact (e.g., fingerprints at crime scene suggesting presence). - A dying declaration is a **direct statement** about the circumstances of death, not requiring inference to establish the fact stated. *Documentary evidence* - **Documentary evidence** consists of written documents, records, or inscriptions presented in court. - A dying declaration is primarily a **verbal statement**, even though it may later be recorded or transcribed in written form.

Q: Which antigen is tested in routine Rh typing?

D antigen. ***D antigen*** - Routine Rh typing specifically tests for the **D antigen**, which determines the Rh status of an individual as Rh-positive or Rh-negative [1]. - The presence of the **D antigen** is crucial for blood transfusions and pregnancy management [1]. *A antigen* - The **A antigen** is tested in the context of the ABO blood group system, not specifically for Rh typing. - It does not provide information regarding the Rh factor which is critical in blood compatibility. *C antigen* - Similar to the **A antigen**, the **C antigen** is part of the broader Rh system but is not routinely assessed in standard Rh typing. - Its testing is typically reserved for specific clinical scenarios involving Rh incompatibility. *B antigen* - The **B antigen** pertains to the ABO blood group and does not relate to the Rh factor or routine Rh typing. - Rh typing is solely focused on the **presence of the D antigen** to determine the Rh status. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Blood And Bone Marrow Disease, pp. 627-628.

Q: Antidepressant drug used in nocturnal enuresis is:

Imipramine. ***Imipramine*** - **Imipramine**, a **tricyclic antidepressant (TCA)**, is frequently used off-label for **nocturnal enuresis** in children [1]. - Its mechanism of action in enuresis is thought to involve a combination of anticholinergic effects (which relax the bladder detrusor muscle) and central nervous system effects (which may increase bladder capacity and arousal from sleep) [1]. *Fluoxetine* - **Fluoxetine** is a **selective serotonin reuptake inhibitor (SSRI)** and is primarily used for depression, anxiety disorders, and OCD [2]. - It is not indicated for the treatment of nocturnal enuresis and does not have the same bladder-relaxing or arousal-modulating properties as imipramine in this context. *Trazodone* - **Trazodone** is a **serotonin antagonist and reuptake inhibitor (SARI)**, commonly prescribed for depression and insomnia due to its prominent sedative effects. - It is not used for nocturnal enuresis and its mechanism of action does not confer benefits for bladder control. *Sertraline* - **Sertraline** is another **selective serotonin reuptake inhibitor (SSRI)** used for a wide range of psychiatric conditions, including depression, anxiety, and panic disorder [2]. - Like fluoxetine, it is not an appropriate treatment for nocturnal enuresis and lacks the specific known effects beneficial for this condition.

Q: Acetaminophen [Paracetamol] induced liver toxicity is due to which metabolite?

NAPQI. ***NAPQI*** - **N-acetyl-p-benzoquinone imine (NAPQI)** is a highly reactive and toxic metabolite produced during acetaminophen metabolism, especially in overdose situations [1, 3]. - When glutathione stores are depleted due to excessive NAPQI formation, this metabolite covalently binds to hepatic macromolecules, causing **hepatocellular damage and necrosis** [1, 3].*N-acetylcysteine* - **N-acetylcysteine (NAC)** is the antidote for acetaminophen overdose, not the toxic metabolite itself [2, 3]. - NAC works by replenishing hepatic **glutathione stores**, which helps detoxify NAPQI and prevent liver injury [2, 3].*Co-Q* - **Coenzyme Q10 (CoQ10)** is an endogenous antioxidant and electron carrier in the mitochondrial respiratory chain. - It is not a metabolite of acetaminophen and plays no direct role in acetaminophen-induced liver toxicity.*Cytochrome 'C'* - **Cytochrome c** is a protein involved in the electron transport chain in mitochondria and plays a critical role in apoptosis. - While cellular damage from NAPQI can eventually lead to cytochrome c release and apoptosis, cytochrome c itself is not a metabolite of acetaminophen or the direct cause of toxicity.

Q: Which of the following statements about ENaC is incorrect?

Composed of 2 homologous subunits. ***Composed of 2 homologous subunits*** - ENaC (Epithelial Sodium Channel) is a **heterotrimeric complex** composed of **three distinct subunits**: α, β, and γ. - The functional channel typically has a stoichiometry of 2α:1β:1γ, forming a heterotrimer. - These subunits share sequence homology but are **non-identical proteins**, not just two homologous subunits. - A fourth related subunit (δ) exists and can substitute for α in some tissues, but the classical ENaC is a three-subunit channel. *Epithelial channel* - ENaC is indeed an **epithelial channel** responsible for critical **sodium reabsorption** in various epithelia. - It plays a vital role in regulating **fluid and electrolyte balance** across tight epithelial layers. *Present in kidney and GIT* - ENaC is abundantly expressed in the **distal nephron of the kidney**, specifically in the collecting duct, where it mediates fine-tuning of sodium reabsorption. - It is also present in the **lower gastrointestinal tract (colon)**, contributing to sodium absorption, and in the airways and salivary glands. *Inhibited by amiloride* - **Amiloride** is a well-known **potassium-sparing diuretic** that specifically acts by blocking ENaC. - This inhibition reduces sodium reabsorption and, consequently, water reabsorption, leading to increased diuresis.

Q: Which hormone is primarily responsible for maintaining the luteal phase of the menstrual cycle?

Progesterone. ***Progesterone*** - **Progesterone**, secreted by the **corpus luteum** after ovulation, is crucial for maintaining the luteal phase by preparing the **endometrium** for implantation. - It causes the endometrial lining to thicken and become more vascularized, creating a suitable environment for a fertilized egg. *Estrogen* - While **estrogen** is important throughout the menstrual cycle for endometrial proliferation, its primary role is in the **follicular phase**, not the maintenance of the luteal phase. - Estrogen levels are higher during the follicular phase, promoting the growth of the dominant follicle. *Follicle-stimulating hormone (FSH)* - **FSH** is primarily responsible for stimulating the growth and development of **ovarian follicles** during the follicular phase. - Its levels decrease significantly after ovulation, and it does not play a direct role in maintaining the luteal phase. *Luteinizing hormone (LH)* - **LH** triggers **ovulation** and the formation of the **corpus luteum** from the ruptured follicle. - While essential for initiating the luteal phase, its levels decline afterward, and it's not the primary hormone for *maintaining* the corpus luteum's function.

Q: What does the transient response observed during the insertion of an electrode in electromyography (EMG) indicate?

Cell membrane disruption. **Cell membrane disruption** - The **transient response** observed during electrode insertion in **EMG** is caused by the mechanical trauma of the needle disrupting the **muscle fiber cell membranes**. - This disruption leads to a brief depolarization and subsequent repolarization of the affected fibers, generating characteristic electrical activity. *Spontaneous muscle activity* - **Spontaneous muscle activity**, such as **fibrillation potentials** or **positive sharp waves**, occurs independently of electrode insertion. - While observed during EMG, these are indicative of **denervation** or **myopathy** and are not directly caused by the act of insertion itself. *Voluntary muscle contraction* - **Voluntary muscle contraction** is recorded when the patient actively contracts the muscle and results in **motor unit action potentials (MUAPs)**. - This is a distinct process from the transient activity produced by electrode insertion. *Induced muscle contraction* - **Induced muscle contraction** typically refers to activity caused by **nerve stimulation** (e.g., in nerve conduction studies) or direct electrical stimulation of the muscle. - This is not the mechanism for the transient response during simple electrode insertion.

Q: All of the following are true about Down syndrome except for one.

Incidence of Robertsonian translocation is 1:1000. **Incidence of Robertsonian translocation is 1:1000** - This statement is **not accurate** for Down syndrome. Robertsonian translocation accounts for only about **3-4% of Down syndrome cases**, not a general population incidence of 1:1000. - The vast majority of Down syndrome cases (~95%) are due to trisomy 21 from nondisjunction, not translocation. - This is the **correct answer** as it is the FALSE statement. *Extra chromosome is of maternal origin* - In approximately **90-95% of Down syndrome cases**, the extra copy of chromosome 21 originates from the mother due to **nondisjunction** during meiosis. - This maternal origin is strongly correlated with **advanced maternal age**. *Most common cause is trisomy 21* - **Trisomy 21** (due to meiotic nondisjunction) accounts for about **95% of all Down syndrome cases**, making it the most common genetic mechanism. - This results in three separate copies of chromosome 21 in all body cells. *Mosaicism 21 has no association with maternal age* - **Mosaic Down syndrome** occurs when nondisjunction happens *after fertilization* in early embryonic development, leading to a mixture of cells with normal and trisomic cells. - Because it is a **post-zygotic event**, its incidence is independent of **maternal age**, unlike full trisomy 21. *Incidence increases with advanced maternal age* - **TRUE statement** - The risk of Down syndrome (particularly trisomy 21) increases significantly with **maternal age**. - Risk is approximately 1:1500 at age 20, 1:1000 at age 30, 1:400 at age 35, and 1:100 at age 40. - This is due to increased risk of meiotic nondisjunction in older oocytes.

Question 1

Coenzyme for phenylalanine hydroxylase is?

Accepted Answer

Tetrahydrobiopterin

Answer

Tetrahydrofolate

Answer

Pyridoxal phosphate

Answer

S-adenosyl methionine

Question 2

What type of evidence is a dying declaration?

Accepted Answer

Oral evidence

Answer

Documentary evidence

Answer

Hearsay evidence

Answer

Circumstantial evidence

Question 3

Which antigen is tested in routine Rh typing?

Accepted Answer

D antigen

Answer

C antigen

Answer

A antigen

Answer

B antigen

Question 4

Antidepressant drug used in nocturnal enuresis is:

Accepted Answer

Imipramine

Answer

Fluoxetine

Answer

Trazodone

Answer

Sertraline

Question 5

Acetaminophen [Paracetamol] induced liver toxicity is due to which metabolite?

Accepted Answer

NAPQI

Answer

Co-Q

Answer

Cytochrome 'C'

Answer

N-acetylcysteine

Question 6

Which of the following statements about ENaC is incorrect?

Accepted Answer

Composed of 2 homologous subunits

Answer

Present in kidney and GIT

Answer

Epithelial channel

Answer

Inhibited by amiloride

Question 7

Which hormone is primarily responsible for maintaining the luteal phase of the menstrual cycle?

Accepted Answer

Progesterone

Answer

Estrogen

Answer

Follicle-stimulating hormone (FSH)

Answer

Luteinizing hormone (LH)

Question 8

What does the transient response observed during the insertion of an electrode in electromyography (EMG) indicate?

Accepted Answer

Cell membrane disruption

Answer

Spontaneous muscle activity

Answer

Voluntary muscle contraction

Answer

Induced muscle contraction

Question 9

What is the PRIMARY mechanism by which the Na+-Ca2+ exchanger functions in cardiac muscle cells?

Accepted Answer

Na+-Ca2+ exchanger acts to remove Ca2+ from heart muscle cells

Answer

Na+-Ca2+ exchanger requires ATP directly

Answer

The Na+-Ca2+ exchanger operates in reverse mode during normal cardiac contraction

Answer

The Na+-Ca2+ exchanger primarily moves Ca2+ into cardiac muscle cells during systole

Question 10

All of the following are true about Down syndrome except for one.

Accepted Answer

Incidence of Robertsonian translocation is 1:1000

Answer

Most common cause is trisomy 21

Answer

Mosaicism 21 has no association with maternal age

Answer

Extra chromosome is of maternal origin

Answer

Incidence increases with advanced maternal age

NEET-PG 2015

Biochemistry

Forensic Medicine

Pathology

Pharmacology

Physiology

Psychiatry