SURUNKALI GEPATITLAR VA HOLETSISTITLARDA YOG’LAR HAZIMLANISHINING BUZILISHI

Authors

  • Abdurasulova Charos Usmonjon qizi Author
  • Saidobbosov Saidmansur Author

Abstract

Yog'larning hazm bo'lishi va so'rilishi energiya gomeostazini saqlashda va muhim fiziologik funktsiyalarni qo'llab-quvvatlashda hal qiluvchi rol o'ynaydi. Yog 'hazm qilishning dastlabki bosqichi oshqozonda sodir bo'ladi, bu erda me'da lipazasi triglitseridlarning gidrolizini boshlaydi. Biroq, yog'larning ko'p hazm bo'lishi oshqozon osti bezi fermentlari va safro tuzlari orqali ingichka ichakda sodir bo'ladi. Yog'ning o't kislotalari bilan emulsifikatsiyasi fermentativ ta'sirni osonlashtiradi, triglitseridlarni erkin yog 'kislotalari va monoglitseridlarga parchalaydi, keyinchalik ular enterotsitlar tomonidan so'rilishi mumkin. Yog 'malabsorbtsiyasi turli xil sabablarga ko'ra yuzaga kelishi mumkin, masalan, ekzokrin oshqozon osti bezi etishmovchiligi, safro kislotasi kasalliklari yoki ichak kasalliklari. Yog 'malabsorbtsiyasining klinik ko'rinishlariga steatoreya, to'yib ovqatlanmaslik va yog'da eriydigan vitaminlarning etishmasligi kiradi. Diagnostik yondashuvlar najasdagi yog 'miqdorini baholashni, tasviriy tadqiqotlarni va o'ziga xos etiologiyani aniqlash uchun turli funktsional testlarni o'z ichiga oladi. Ushbu sharh maqolasida yog'larning hazm bo'lishi va so'rilishining normal fiziologik jarayoni tasvirlanadi va oshqozon-ichak traktida yog'larning so'rilishiga olib kelishi mumkin bo'lgan turli xil patofiziologiyalar, shuningdek, ularning tegishli diagnostik tekshiruv usullari muhokama qilinadi. Yog'ning samarali hazm bo'lishi umumiy salomatlik uchun juda muhimdir, chunki u ko'plab muhim oziq moddalarni o'zlashtirishga imkon beradi, hujayra va tizimli funktsiyalarda ajralmas rol o'ynaydi va tanani energiya bilan ta'minlaydi. Bu disfunktsiyali bo'lsa, malabsorbtsiya buzilishlari paydo bo'lishi mumkin. Ushbu maqola sog'lom odamlarda yog'larning hazm bo'lishi va so'rilishining fiziologik jarayoni haqida qisqacha ma'lumot beradi, shuningdek, oshqozon-ichak traktida yog'larning malabsorbtsiyasiga olib kelishi mumkin bo'lgan muhim patofiziologiyani va hozirgi diagnostik test usullarini ko'rib chiqadi.

References

1. B S, Gokak A V, Bellad A. (2025). Obstructive Jaundice Secondary to Choledocholithiasis With Chronic Cholecystitis. Cureus, 17(8): e91041. DOI 10.7759/cureus.91041

2. Rinawi F. (2015). Fat malabsorption and bile acid synthesis defect. IMAJ — Israel Medical Association Journal, Vol. 17, March 2015, pp. 190–191. www.ima.org.il

3. O‘zbek Vikipediya. Yog’. https://uz.wikipedia.org/wiki/Yog‘ (murojaat sanasi: 2026)

4. Schirmer B.D., Winters K.L., Edlich R.F. (2005). Cholelithiasis and cholecystitis. J Long Term Eff Med Implants, 15:329–38. DOI 10.1615/jlongtermeffmedimplants.v15.i3.90

5. Yadav G.D., Yadav A., Verma S., Hussain M.T. (2022). Clinical profile, management, and outcome of obstructive jaundice patient at a tertiary care center: a prospective study. Asian J Med Sci, 13:94–9. DOI 10.3126/ajms.v13i5.42527

6. Kumar V., Abbas A.K., Aster J.C. (2020). Robbins & Cotran Pathologic Basis of Disease. Elsevier.

7. Sahu S.K., Nath P., Mallick B., Praharaj D., Giri S., Panigrahi S.C., Anand A.C. (2024). Etiological profile of obstructive jaundice and acute cholangitis: three-year data from a tertiary care center in eastern India. Euroasian J Hepatogastroenterol, 14:187–90. DOI 10.5005/jp-journals-10018-1448

8. Alfehaidi M. (2022). Laparoscopic cholecystectomy for a giant gallstone: a case report. Cureus, 14:e31546. DOI 10.7759/cureus.31546

9. Gao Y., He D., Feng W., Yue J., Jian Z. (2023). Laparoscopic cholecystectomy for giant gallbladder: a case report. Medicine (Baltimore), 102:e35429. DOI 10.1097/MD.0000000000035429

10. Igwe P.O., Diri O.N. (2020). Laparoscopic cholecystectomy for giant gall stone: report of two cases. Int J Surg Case Rep, 67:107–10. DOI 10.1016/j.ijscr.2020.01.055

11. Jayant M., Dalal A.K., Attri A.K., Sachdev A. (2010). Giant staghorn stone in common bile duct. Indian J Gastroenterol, 29:212. DOI 10.1007/s12664-010-0054-8

12. Vinay V., Kumar N.S., Khan O., Azharudin S.K. (2024). Giant choledocholithiasis with choledochal cyst: a report of a rare case. Cureus, 16:e64306. DOI 10.7759/cureus.64506

13. Nissen T., Wynn R. (2014). The clinical case report: a review of its merits and limitations. BMC Res Notes, 7:264. DOI 10.1186/1756-0500-7-264

14. Clayton P.T. (2011). Disorders of bile acid synthesis. J Inherit Metab Dis, 34:593–604.

15. Gonzales E.M., Gendhardt M.A., Fabre M.O. et al. (2009). Oral cholic acid for hereditary defects of primary bile acid synthesis: a safe and effective long-term therapy. J Pediatr Gastroenterol Nutr, 49:117–20.

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Published

2026-05-20