The document discusses endocrine glands and hormones. It explains that endocrine glands secrete hormones directly into the bloodstream, lacking ducts, and hormones are carried to target cells containing receptors. Hormones affect metabolism and regulate body processes like growth and reproduction. The mechanisms of hormone action depend on their chemical structure, with some binding to nuclear receptors to alter gene expression and others using second messengers to enact cellular responses. The pituitary gland is described as having anterior and posterior lobes that secrete trophic and regulatory hormones under control of the hypothalamus.
A TRIANGULAR GLAND, WHICH HAS BOTH EXOCRINE AND ENDOCRINE CELLS, LOCATED BEHIND THE STOMACHACINAR CELLS PRODUCE AN ENZYME-RICH JUICE USED FOR DIGESTION (EXOCRINE PRODUCT)PANCREATIC ISLETS (ISLETS OF LANGERHANS) PRODUCE HORMONES INVOLVED IN REGULATING FUEL STORAGE AND USE.
Here is another topic named as sex hormones of both male and female. you get all the info from this presentation about this topic. Hope you will like it and get beneficial for you.
A TRIANGULAR GLAND, WHICH HAS BOTH EXOCRINE AND ENDOCRINE CELLS, LOCATED BEHIND THE STOMACHACINAR CELLS PRODUCE AN ENZYME-RICH JUICE USED FOR DIGESTION (EXOCRINE PRODUCT)PANCREATIC ISLETS (ISLETS OF LANGERHANS) PRODUCE HORMONES INVOLVED IN REGULATING FUEL STORAGE AND USE.
Here is another topic named as sex hormones of both male and female. you get all the info from this presentation about this topic. Hope you will like it and get beneficial for you.
Slides prepared MBBS Biochemistry lectures. Includes description of hormone signaling, hormone actions, detailed description of insulin and diabetes mellitus, metabolic syndrome, thyroid hormones, calcium and phosphate homeostasis, vitamin D and PTH.
Prepared in Nov 2015
Definitions of GI bleeding
GI Bleeding include Upper and Lower of GIB
Causes of GI bleeding
Pathogenesis of GI bleeding
Diagnosis of GI bleeding
Clinical of GI bleeding
Management of GI bleeding
Recommendation of GI bleeding
Clinical guideline of GI bleeding
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TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
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Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
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New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
2. Endocrine Glands and Hormones
Secrete biologically
active molecules into
the blood.
◦ Lack ducts.
Carry hormones to
target cells that
contain specific
receptor proteins for
that hormone.
Target cells can
respond in a specific
fashion.
3. Endocrine Glands and Hormones
(continued)
• Neurohormone:
▫ Specialized neurons that secrete chemicals into the
blood rather than synaptic cleft.
Chemical secreted is called neurohormone.
• Hormones:
▫ Affect metabolism of target organs.
Help regulate total body metabolism, growth, and
reproduction.
4. Chemical Classification of Hormones
• Amines:
▫ Hormones derived from tyrosine and tryptophan.
NE, Epi, T4.
• Polypeptides and proteins:
▫ Polypeptides:
Chains of < 100 amino acids in length.
ADH.
▫ Protein hormones:
Polypeptide chains with > 100 amino acids.
Growth hormone.
5. Chemical Classification of
Hormones (continued)
• Lipids derived from cholesterol.
▫ Are lipophilic hormones.
Testosterone.
Estradiol.
Cortisol.
Progesterone.
7. Chemical Classification of Hormones
(continued)
Glycoproteins:
◦ Long polypeptides (>100) bound to 1 or more
carbohydrate (CHO) groups.
FSH and LH.
Hormones can also be divided into:
◦ Polar:
H20 soluble.
◦ Nonpolar (lipophilic):
H20 insoluble.
Can gain entry into target cells.
Steroid hormones and T4.
◦ Pineal gland secretes melatonin:
Has properties of both H20 soluble and lipophilic hormones.
8. Prohormones and Prehormones
• Prohormone:
▫ Precursor is a longer chained polypeptide that is
cut and spliced together to make the hormone.
Proinsulin.
• Preprohormone:
▫ Prohormone derived from larger precursor
molecule.
Preproinsulin.
• Prehormone:
▫ Molecules secreted by endocrine glands that are
inactive until changed into hormones by target
cells.
T4 converted to T3.
9. Common Aspects of Neural and Endocrine
Regulation
• APs are chemical events produced by diffusion of ions
through neuron plasma membrane.
• Action of some hormones are accompanied by ion
diffusion and electrical changes in the target cell.
▫ Nerve axon boutons release NTs.
▫ Some chemicals are secreted as hormones, and also are NTs.
• In order for either a NT or hormone to function in
physiological regulation:
▫ Target cell must have specific receptor proteins.
▫ Combination of the regulatory molecule with its receptor
proteins must cause a specific sequence of changes.
▫ There must be a mechanism to quickly turn off the action of a
regulator.
10. Hormonal Interactions
• Synergistic:
▫ Two hormones work together to produce a
result.
▫ Additive:
Each hormone separately produces response,
together at same concentrations stimulate even
greater effect.
NE and Epi.
▫ Complementary:
Each hormone stimulates different step in the
process.
FSH and testosterone.
11. Hormonal Interactions (continued)
▫ Permissive effects:
Hormone enhances the responsiveness of a
target organ to second hormone.
Increases the activity of a second hormone.
▫ Prior exposure of uterus to estrogen induces formation of
receptors for progesterone.
▫ Antagonistic effects:
Action of one hormone antagonizes the effects of
another.
Insulin and glucagon.
12. Effects of [Hormone] on Tissue
Response
• [Hormone] in blood reflects the rate of
secretion.
• Half-life:
▫ Time required for the blood [hormone] to be reduced
to ½ reference level.
Minutes to days.
• Normal tissue responses are produced only
when [hormone] are present within
physiological range.
• Varying [hormone] within normal,
physiological range can affect the
responsiveness of target cells.
13. Effects of [Hormone] on Tissue
Response (continued)
• Priming effect (upregulation):
▫ Increase number of receptors formed on target
cells in response to particular hormone.
▫ Greater response by the target cell.
• Desensitization (downregulation):
▫ Prolonged exposure to high [polypeptide
hormone].
Subsequent exposure to the same [hormone] produces less
response.
Decrease in number of receptors on target cells.
▫ Insulin in adipose cells.
▫ Pulsatile secretion may prevent downregulation.
14. Mechanisms of Hormone Action
• Hormones of same chemical class have similar
mechanisms of action.
▫ Similarities include:
Location of cellular receptor proteins depends on
the chemical nature of the hormone.
Events that occur in the target cells.
• To respond to a hormone:
▫ Target cell must have specific receptors for that
hormone (specificity).
Hormones exhibit:
Affinity (bind to receptors with high bond strength).
Saturation (low capacity of receptors).
15. Hormones That Bind to Nuclear
Receptor Proteins
• Lipophilic steroid and
thyroid hormones are
attached to plasma
carrier proteins.
▫ Hormones dissociate from
carrier proteins to pass
through lipid component
of the target plasma
membrane.
• Receptors for the
lipophilic hormones are
known as nuclear
hormone receptors.
16. Nuclear Hormone Receptors
• Steroid receptors are located in cytoplasm and in the
nucleus.
• Function within cell to activate genetic transcription.
▫ Messenger RNA directs synthesis of specific enzyme proteins
that change metabolism.
• Each nuclear hormone receptor has 2 regions:
▫ A ligand (hormone)-binding domain.
▫ DNA-binding domain.
• Receptor must be activated by binding to hormone
before binding to specific region of DNA called HRE
(hormone responsive element).
▫ Located adjacent to gene that will be transcribed.
17. Mechanisms of Steroid Hormone
Action
• Cytoplasmic receptor
binds to steroid hormone.
• Translocates to nucleus.
• DNA-binding domain
binds to specific HRE of
the DNA.
• Dimerization occurs.
▫ Process of 2 receptor units
coming together at the 2
half-sites.
• Stimulates transcription
of particular genes.
18. Mechanism of Thyroid Hormone Action
• T4 passes into cytoplasm and
is converted to T3.
• Receptor proteins located in
nucleus.
▫ T3 binds to ligand-binding
domain.
▫ Other half-site is vitamin A
derivative (9-cis-retinoic)
acid.
DNA-binding domain can
then bind to the half-site of
the HRE.
▫ Two partners can bind to the
DNA to activate HRE.
Stimulate transcription of
genes.
19. Hormones That Use 2nd
Messengers
• Hormones cannot pass through plasma
membrane use 2nd
messengers.
▫ Catecholamine, polypeptide, and glycoprotein
hormones bind to receptor proteins on the
target plasma membrane.
• Actions are mediated by 2nd
messengers
(signal-transduction mechanisms).
▫ Extracellular hormones are transduced into
intracellular 2nd
messengers.
20. Adenylate Cyclase-cAMP
• Polypeptide or glycoprotein hormone binds to
receptor protein causing dissociation of a
subunit of G-protein.
• G-protein subunit binds to and activates
adenylate cyclase.
• ATP cAMP + PPi
• cAMP attaches to inhibitory subunit of
protein kinase.
• Inhibitory subunit dissociates and activates
protein kinase.
21. Adenylate Cyclase-cAMP (continued)
• Phosphorylates
enzymes within the
cell to produce
hormone’s effects.
• Modulates activity of
enzymes present in
the cell.
• Alters metabolism of
the cell.
• cAMP inactivated by
phosphodiesterase.
▫ Hydrolyzes cAMP
to inactive
fragments.
22. Phospholipase-C-Ca2+
• Binding of Epi to α-adrenergic receptor in
plasma membrane activates a G-protein
intermediate, phospholipase C.
▫ Phospholipase C splits phospholipid into IP3
and DAG.
Both derivatives serve as 2nd
messengers.
• IP3 diffuses through cytoplasm to ER.
▫ Binding of IP3 to receptor protein in ER causes
Ca2+
channels to open.
25. Tyrosine Kinase
• Insulin receptor consists of 2 units that dimerize
when they bind with insulin.
▫ Insulin binds to ligand–binding site on plasma
membrane, activating enzymatic site in the cytoplasm.
• Autophosphorylation occurs, increasing tyrosine
kinase activity.
• Activates signaling molecules.
▫ Stimulate glycogen, fat and protein synthesis.
▫ Stimulate insertion of GLUT-4 carrier proteins.
27. Pituitary Gland
• Pituitary gland
is located in the
diencephalon.
• Structurally and
functionally
divided into:
▫ Anterior lobe.
▫ Posterior lobe.
28. Pituitary Gland (continued)
• Anterior pituitary:
▫ Master gland (adenohypophysis).
▫ Derived from a pouch of epithelial tissue that
migrates upward from the mouth.
Consists of 2 parts:
Pars distalis: anterior pituitary.
Pars tuberalis: thin extension in contact with the infundibulum.
• Posterior pituitary(neurohypophysis):
▫ Formed by downgrowth of the brain during fetal
development.
▫ Is in contact with the infundibulum.
Nerve fibers extend through the infundibulum.
29. Pituitary Hormones
• Anterior
Pituitary:
▫ Trophic effects:
High blood
[hormone] causes
target organ to
hypertrophy.
Low blood
[hormone] causes
target organ to
atrophy.
30. Pituitary Hormones (continued)
• Posterior pituitary:
▫ Stores and releases 2 hormones that are
produced in the hypothalamus:
Antidiuretic hormone (ADH/vasopressin):
Promotes the retention of H20 by the kidneys.
▫ Less H20 is excreted in the urine.
Oxytocin:
Stimulates contractions of the uterus during parturition.
Stimulates contractions of the mammary gland alveoli.
▫ Milk-ejection reflex.
31. Hypothalamic Control of Posterior
Pituitary
• Hypothalamus neuron
cell bodies produce:
▫ ADH: supraoptic nuclei.
▫ Oxytocin:
paraventricular nuclei.
• Transported along the
hypothalamo-
hypophyseal tract.
• Stored in posterior
pituitary.
• Release controlled by
neuroendocrine
reflexes.
32. Hypothalamic Control of the
Anterior Pituitary
• Hormonal control rather
than neural.
• Hypothalamus neurons
synthesize releasing and
inhibiting hormones.
• Hormones are
transported to axon
endings of median
eminence.
• Hormones secreted into
the hypothalamo-
hypophyseal portal
system regulate the
secretions of the anterior
pituitary
33. Feedback Control of the Anterior
Pituitary
• Anterior pituitary and hypothalamic
secretions are controlled by the target organs
they regulate.
▫ Secretions are controlled by negative feedback
inhibition by target gland hormones.
• Negative feedback at 2 levels:
▫ The target gland hormone can act on the
hypothalamus and inhibit secretion of releasing
hormones.
▫ The target gland hormone can act on the anterior
pituitary and inhibit response to the releasing
hormone.
34. Feedback Control of the Anterior
Pituitary (continued)
• Short feedback loop:
▫ Retrograde transport of
blood from anterior
pituitary to the
hypothalamus.
Hormone released by
anterior pituitary
inhibits secretion of
releasing hormone.
• Positive feedback
effect:
▫ During the menstrual
cycle, estrogen
stimulates “LH surge.”
35. Higher Brain Function and Pituitary
Secretion
• Axis:
▫ Relationship between anterior pituitary and a
particular target gland.
Pituitary-gonad axis.
• Hypothalamus receives input from higher brain
centers.
▫ Psychological stress affects:
Circadian rhythms.
Menstrual cycle.
36. Adrenal Glands
• Paired organs that cap the kidneys.
• Each gland consists of an outer cortex and inner
medulla.
• Adrenal medulla:
▫ Derived from embryonic neural crest ectoderm
(same tissue that produces the sympathetic
ganglia).
▫ Synthesizes and secretes:
Catecholamines (mainly Epi but some NE).
37. Adrenal Glands (continued)
• Adrenal cortex:
▫ Does not receive
neural innervation.
▫ Must be stimulated
hormonally (ACTH).
• Consists of 3 zones:
▫ Zona glomerulosa.
▫ Zona fasciculata.
▫ Zona reticularis.
• Secretes
corticosteroids.
38. Functions of the Adrenal Cortex
• Zona glomerulosa:
▫ Mineralcorticoids (aldosterone):
Stimulate kidneys to reabsorb Na+
and secrete
K+
.
• Zona fasciculata:
▫ Glucocorticoids (cortisol):
Inhibit glucose utilization and stimulate
gluconeogenesis.
• Zona reticularis (DHEA):
▫ Sex steroids:
Supplement sex steroids.
40. Functions of the Adrenal Medulla
• Innervated by preganglionic sympathetic axons.
▫ Increase respiratory rate.
▫ Increase HR and cardiac output.
▫ Vasoconstrict blood vessels, thus increasing
venous return.
▫ Stimulate glycogenolysis.
▫ Stimulate lipolysis.
41. Stress and the Adrenal Gland
• Non-specific response
to stress produces the
general adaptation
syndrome (GAS).
• Alarm phase:
▫ Adrenal glands
activated.
• Stage of resistance:
▫ Stage of readjustment.
• Stage of exhaustion:
▫ Sickness and/or death if
readjustment is not
complete.
42. Thyroid Hormones
• Thyroid gland is located
just below the larynx.
• Thyroid is the largest of
the pure endocrine
glands.
• Follicular cells secrete
thyroxine.
• Parafollicular cells
secrete calcitonin.
43. Production of Thyroid Hormones
• Iodide (I-
) actively transported into the
follicle and secreted into the colloid.
• Oxidized to iodine (Io
).
• Iodine attached to tyrosine within
thyroglobulin chain.
▫ Attachment of 1 iodine produces monoiodotyrosine
(MIT).
▫ Attachment of 2 iodines produces diiodotyrosine
(DIT).
• MIT and DIT or 2 DIT molecules coupled
together.
44. Production of Thyroid Hormones
(continued)
• T3 and T4 produced.
• TSH stimulates pinocytosis into the
follicular cell.
▫ Enzymes hydrolyze T3 and T4from thyroglobulin.
• Attached to TBG and released into blood.
46. Actions of T3
• Stimulates protein synthesis.
• Promotes maturation of nervous system.
• Stimulates rate of cellular respiration by:
▫ Production of uncoupling proteins.
▫ Increase active transport by Na+
/K+
pumps.
▫ Lower cellular [ATP].
• Increases metabolic heat.
• Increases metabolic rate.
▫ Stimulates increased consumption of glucose, fatty
acids and other molecules.
47. Diseases of the Thyroid
• Iodine-deficiency
(endemic) goiter:
▫ Abnormal growth of
the thyroid gland.
In the absence of
sufficient iodine, cannot
produce adequate
amounts of T4 and T3.
Lack of negative
feedback inhibition.
▫ Stimulates TSH, which
causes abnormal
growth.
48. Diseases of the Thyroid (continued)
[Iodine-deficiency (endemic) goiter—continued]
▫ Adult myxedema:
Accumulation of mucoproteins and fluid in subcutaneous tissue.
▫ Symptoms:
Decreased metabolic rate.
Weight gain.
Decreased ability to adapt to cold.
Lethargy.
• Grave’s disease:
▫ Autoimmune disorder:
Exerts TSH-like effects on thyroid.
Not affected by negative feedback.
• Cretinism:
▫ Hypothyroid from end of 1st
trimester to 6 months postnatally.
Severe mental retardation.
49. Parathyroid Glands
• Embedded in the lateral
lobes of the thyroid gland.
• Parathyroid hormone
(PTH):
▫ Only hormone secreted by
the parathyroid glands.
• Single most important
hormone in the control of
blood [Ca2+
].
• Stimulated by decreased
blood [Ca2+
].
• Promotes rise in blood [Ca2+
]
by acting on bones, kidney
and intestines.
50. Pancreatic Islets (Islets of
Langerhans)
• Alpha cells secrete glucagon.
▫ Stimulus is decrease in blood
[glucose].
▫ Stimulates glycogenolysis
and lipolysis.
▫ Stimulates conversion of
fatty acids to ketones.
• Beta cells secrete insulin.
▫ Stimulus is increase in blood
[glucose].
▫ Promotes entry of glucose
into cells.
▫ Converts glucose to glycogen
and fat.
▫ Aids entry of amino acids
into cells.
51. Pineal Gland
• Secretes melatonin:
▫ Production stimulated by the suprachiasmatic nucleus (SCN)
in hypothalamus.
SCN is primary center for circadian rhythms.
Light/dark changes required to synchronize.
Melatonin secretion increases with darkness and peaks in middle
of night.
▫ May inhibit GnRH.
▫ May function in the onset of puberty (controversial).
53. Thymus
• Site of production of T cells (thymus-dependent
cells), which are lymphocytes.
▫ Lymphocytes are involved in cell-mediated immunity.
• Secretes hormones that are believed to stimulate
T cells after leave thymus.
▫ Thymus gland size is large in newborns and children.
• Regresses after puberty and becomes infiltrated
with strands of fibrous tissue.
54. Gonads and Placenta
• Gonads (testes and ovaries):
▫ Secrete sex hormones.
Testosterone.
Estradiol 17-β.
After menopause, produces estrone.
Progesterone.
• Placenta:
▫ Secretes large amounts of estriol, progesterone,
hCG, hCS.
55. Autocrine and Paracrine Regulation
• Autocrine:
▫ Produced and act within the same tissue of an organ.
All autocrine regulators control gene expression in target cells.
• Paracrine:
▫ Produced within one tissue and regulate a different tissue of
the same organ.
• Cytokines (lymphokines):
▫ Regulate different cells (interleukins) .
• Growth factors:
▫ Promote growth and cell division in any organ.
• Neutrophins:
▫ Guide regenerating peripheral neurons.
56. Prostaglandins
• Most diverse group of autocrine regulators.
• Produced in almost every organ.
• Wide variety of functions.
• Different prostaglandins may exert antagonistic
effects in some tissues.
▫ Immune system:
Promote inflammatory process.
▫ Reproductive system:
Play role in ovulation.
▫ Digestive system:
Inhibit gastric secretion.