Application of 2-bromopalmitic acid in preparation of medicine for treating spermatogenic dysfunction related diseases
A dysfunctional, bromopalmitic acid technology, applied in the field of biomedicine, to restore the integrity of the blood-testis barrier and improve spermatogenic dysfunction
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Embodiment 1
[0030] The example of 2-bromopalmitic acid improving the barrier damage of Sertoli cells stimulated by saturated fatty acids in vitro is as follows.
[0031] (1) Isolation and culture of mouse primary Sertoli cells:
[0032] Take 20-day-old ICR male mice, kill them by neck dislocation, soak them in 75% disinfectant alcohol for 2-5 minutes, incise the skin of the lower abdomen in an ultra-clean bench, take out the testes, cut off the seminal vesicles from the tail of the epididymis, take both testes, and put them in In a culture dish of PBS at 37°C, use ophthalmic tweezers to tear off adipose tissue, testicular tunica and blood vessels, expose the seminiferous tubules, and put them into another culture dish with PBS. Cut tissue to less than 1mm 3 Put them in 5ml d0.25% (m / V) trypsin, shake and digest at 37°C for 4-6 minutes to disperse the seminiferous tubules. Wash once with 25-30ml of PBS, remove the supernatant. Digest with 5ml 0.1% (m / V) type 1 collagenase at 37°C for 6-...
Embodiment 2
[0047] 2-Bromopalmitic acid can significantly improve spermatogenic dysfunction and blood-testis barrier damage caused by lipid metabolism disorders in vivo. Examples are as follows.
[0048] (1) Selection of experimental materials:
[0049] 4-week-old ICR male mice were selected as animals; 2-BP and PA were selected from Sigma Company of the United States. 2-BP was prepared as a 100 mg / ml storage solution with ethanol, and was injected with physiological saline as a 5 mg / ml working solution during the experiment. PA was chelated with BSA and prepared into a 20 mM (about 5.13 mg / ml) storage solution (ie, working solution) with physiological saline as a solvent.
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