Sperm cells get energy to power their movement from secreted by the
fructose; seminal glands
fructose; prostate gland
glucose; bulbourethral glands
glucose; seminal glands
fructose; seminiferous gland
The Correct Answer is A
A. fructose; seminal glands: The seminal vesicles (seminal glands) secrete a viscous fluid that contains high concentrations of fructose. This monosaccharide serves as the primary glycolytic fuel for the mitochondria in the sperm midpiece to produce ATP. This energy is essential for the flagellar lashing required for motility.
B. fructose; prostate gland: While the prostate contributes citrate and enzymes to the semen, it is not the primary source of the sugar used for sperm energetics. The prostatic fluid is slightly acidic and focuses more on the activation of sperm and the liquefaction of the coagulum. Fructose production is localized to the seminal vesicles.
C. glucose; bulbourethral glands: The bulbourethral glands primarily secrete a clear mucus that serves to lubricate the urethra and neutralize acidic urine. They do not produce significant quantities of simple sugars like glucose or fructose for sperm nutrition. Their contribution is protective and preparatory rather than nutritive.
D. glucose; seminal glands: Although glucose is the common metabolic sugar in the blood, the seminal glands specifically synthesize and secrete fructose. Fructose is preferred in the seminal environment and is the standard marker used in clinical labs to verify the secretory function of the seminal vesicles. Glucose is not the primary seminal sugar.
E. fructose; seminiferous gland: There is no anatomical structure officially termed a "seminiferous gland." The seminiferous tubules are the site of sperm production, but the fluid they produce is minimal and lacks the concentrated nutrient load found in the secretions of the accessory glands. Fructose is added later in the ductal system.
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Related Questions
Correct Answer is B
Explanation
A. 6 months: While spermatogenesis is a continuous process, the duration required for a single spermatogonium to become a mature spermatozoon is significantly shorter than half a year. Estimating 6 months overestimates the temporal requirements of the seminiferous epithelium. The cycle of the human germinal epithelium is a relatively rapid biological turnover.
B. 3-4 months: The complete process of spermatogenesis, including the mitotic and meiotic divisions followed by spermiogenesis, takes approximately 64 to 72 days. When combined with the subsequent maturation and transit time through the epididymis, the total time to manufacture a viable, motile sperm is roughly 90 to 120 days. This reflects the standard physiological timeline for male gametogenesis.
C. one year: A one-year duration would result in an extremely slow recovery of fertility after any insult to the testes. Human males produce millions of sperm daily, which is only possible through a much faster developmental cycle. The germ cells progress through their developmental stages in a matter of months, not years.
D. 28 days: This timeframe is more characteristic of the human female ovarian and menstrual cycles. Spermatogenesis is a more complex and lengthy process involving significant morphological changes during the spermiogenesis phase. Four weeks is insufficient time for a spermatogonium to complete the transformation into a fully differentiated, viable spermatozoon.
Correct Answer is A
Explanation
A. osmosis. Water moves passively across the renal tubular epithelium following osmotic gradients established by the active transport of solutes like sodium. This process, often referred to as obligatory water reabsorption in the proximal tubule, allows water to diffuse through aquaporins. It does not require direct ATP consumption for the water molecules themselves.
B. filtration. Filtration is the process that occurs exclusively in the renal corpuscle where blood is processed into filtrate. Once the fluid enters the renal tubules, the movement of substances back into the blood is classified as reabsorption. Filtration is driven by hydrostatic pressure, whereas tubular water movement is driven by osmotic concentration differences.
C. active transport. There are no known biological pumps that directly use ATP to move water molecules against a concentration gradient. Biological systems move water by actively transporting solutes and allowing water to follow passively. All water movement in the kidney is a response to osmotic or hydrostatic forces rather than direct active pumping.
D. cotransport with sodium ions. While many solutes like glucose and amino acids use secondary active transport (cotransport) with sodium, water moves through separate channel proteins called aquaporins. Sodium reabsorption creates the osmotic drive, but the water molecules do not bind to the carrier proteins alongside sodium. Water movement is the result of the sodium transport, not a shared transport mechanism.
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