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Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

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Page 1: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-1

Chapter 41Animal Nutrition

Taken in

Taken apart

Taken up

Page 2: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-4

Page 3: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-6a

Humpback whale, a suspension feeder

Baleen

Fig. 41-6b

Leaf miner caterpillar,a substrate feeder

Mosquito, a fluid feederRock python, a bulk feeder

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Fig. 41-18

Incisors

(c) Omnivore

Molars

(b) Herbivore

(a) Carnivore

Canines Premolars

Evolutionary and Adaptations

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Fig. 41-9Esophagus

Mouth

Pharynx

Crop Gizzard

Typhlosole

Intestine

Lumen of intestine

Anus

(b) Grasshopper

Foregut

(c) Bird

(a) Earthworm

Midgut Hindgut

Esophagus RectumAnus

Mouth

Crop

Gastric cecae

Esophagus

Mouth

Crop

Anus

StomachGizzard

Intestine

Variation in alimentary canals

Page 6: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-19

Cecum

Small intestine

HerbivoreCarnivore

Colon(largeintestine)

StomachSmall intestine

Stomach and intestinal adaptions

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Fig. 41-20

Esophagus

OmasumAbomasum

Intestine

Rumen Reticulum1 2

43

Mutualistic adaptation瘤胃

蜂巢胃

重瓣胃皺胃

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Concept 41.2: The main stages of food processing are ingestion, digestion, absorption, and elimination

Ingestion Digestion Absorption Elimination

Undigestedmaterial

Chemical digestion(enzymatic hydrolysis)

Nutrientmoleculesenter bodycells

Smallmolecules

Mechanicaldigestion

Food

Piecesof food

1 2 3 4

Page 9: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-10a

Cecum

Anus

Ascendingportion oflarge intestine

Gall-bladder

Smallintestine

Largeintestine

Smallintestine

Rectum

Pancreas

Liver

Salivary glands

TongueOral cavity

Pharynx

Esophagus

Sphincter

Stomach

Sphincter

Duodenum ofsmall intestine

Appendix

Peristalsis

sphincters

Page 10: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

Essential Nutrients

• There are four classes of essential nutrients:

– Essential amino acids

– Essential fatty acids

– Vitamins

– Minerals

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Beans and otherlegumes

Corn (maize)and other grains

Lysine

Essential amino acids for adults

Tryptophan

Isoleucine

Leucine

Phenylalanine

Threonine

ValineMethionine

insufficient essential amino acids-----Malnutrition or called protein deficiency

•Vegetarian diet---

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Fig. 41-3

Storing protein for growth

Muscle protein

Feather protein

Page 13: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

Essential Fatty Acids

• Animals can synthesize most of the fatty acids they need

• The essential fatty acids are certain unsaturated fatty acids that must be obtained from the diet

• Deficiencies in fatty acids are rare

Page 14: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

Unsaturated fatty acids

– Palmitoleic acid (16:1): 棕櫚烯酸

– Oleic acid (18:1): 油酸

– Linoleic acid (18:2): 亞麻油酸

– -Linolenic acid (18:3): α- 亞麻油酸

– Arachidonic acid (20:4): 花生四烯酸

– -Linolenic acid (18:3): γ- 亞麻油酸

– Linoleic acid – Arachidonic acid – eicosanoids -- postaglandins

動物無法合成

植物沒有

Page 15: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

羅倫佐的油

• 羅倫佐得了什麼病?adrenoleukodystrophy (ALD) 腎上腺腦白質退化症

• 過氧化小體 (peroxisome)

– 「非常長鏈飽和性脂肪酸」 (very long-chain fatty acids, VLCFA) 特別是 C24 、 C26的代謝異常

http://www.myelin.org/aboutlorenzo.htm

Page 16: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

Vitamins

• Vitamins are organic molecules required in the diet in small amounts

• 13 vitamins essential to humans have been identified

• Vitamins are grouped into two categories: fat-soluble and water-soluble

Page 17: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

Assessing Nutritional NeedsCan diet influence the frequency of birth

defects?

• Insights into human nutrition have come from

epidemiology, the study of human health and disease in populations

• Richard Smithells

-Women who had had one or more babies with neural tube defect.

Page 19: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

Dietary Deficiencies

• Undernourishment

• Malnourishment

• Overnourishment

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Fig. 41-21

Homeostasis:90 mg glucose/100 mL blood

Stimulus:Blood glucose

level risesafter eating.

Stimulus:Blood glucose

level dropsbelow set point.

Hometic regulation of cellular fuel

Role of blood glucose in providing energy

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Absorptive phase

Page 22: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Postabsorptive state

Page 23: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-12

Interior surfaceof stomach

Esophagus

Chief cells

Small intestine

Epithelium

Stomach

Sphincter

Parietal cell

Pepsinogen and HClare secreted.

HCl convertspepsinogen to pepsin.

Pepsin activatesmore pepsinogen.

Chief cell

Folds ofepithelialtissue

Pepsin

Sphincter

Pepsinogen

HCl

H+

Cl–

Parietal cells

Mucus cells

Gastric gland

1

2

2

3

3

1

5 µ

m

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Fig. 41-UN1

Bloodstream

Veins to heart

Lymphaticsystem

Small intestine

Esophagus

StomachLipids

Mouth

Hepatic portal vein

Absorbed food(except lipids)

Absorbedwater

Secretions fromthe gastric glandsof the stomach

Secretions from the pancreas and the liver

Liver

Rectum

Anus

Largeintestine

Page 25: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-10b

Anus

Liver

Pancreas

Smallintestine

Largeintestine

Rectum

Stomach

Gall-bladder

A schematic diagram of thehuman digestive system

Esophagus

Salivaryglands

Mouth

Page 26: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-12b

Interior surfaceof stomach

Chief cells

Epithelium

Parietal cell

Pepsinogen and HClare secreted.

HCl convertspepsinogen to pepsin.

Pepsin activatesmore pepsinogen.

Chief cell

PepsinPepsinogen

HCl

H+

Cl–

Parietal cells

Mucus cells

Gastric gland2

3

1

1

2

3

•Helicobacter pylori

Page 27: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-15

Muscle layers

Microvilli (brushborder) at apical(lumenal) surface

Vein carrying bloodto hepatic portal vein

Villi

Intestinal wall

Key

Nutrientabsorption

Largecircularfolds

Bloodcapillaries

Epithelialcells

Villi

Lymphvessel

Basal surface

Lacteal

Epithelial cells

Lumen

The structure of the small intestine

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Fig. 41-13

Oral cavity,pharynx,esophagus

Stomach

Lumen ofsmall intes-tine

Epitheliumof smallintestine(brushborder)

Carbohydrate digestion

Polysaccharides

Smaller polysaccharides,maltose

Polysaccharides

Maltose and otherdisaccharides

Disaccharides

Protein digestion Nucleic acid digestion Fat digestion

Proteins

Small polypeptides

Pepsin

Pancreatic amylases

Salivary amylase

Disaccharidases

Monosaccharides

Small peptides

Amino acids

Amino acids

Polypeptides

Smallerpolypeptides

Pancreatic trypsin andchymotrypsin

Pancreatic carboxypeptidase

Dipeptidases, carboxypeptidase,and aminopeptidase

DNA, RNA

Pancreatic nucleases

Fat globules

NucleotidesFat droplets

Nucleosides

Nitrogenous bases,sugars, phosphates

Nucleotidases

Nucleosidasesandphosphatases

Glycerol, fattyacids, monoglycerides

Bile salts

Pancreatic lipase

(starch, glycogen) (sucrose, lactose)

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Fig. 41-13a

Oral cavity,pharynx,esophagus

Stomach

Lumen ofsmall intestine

Epitheliumof smallintestine(brushborder)

Carbohydrate digestion

Polysaccharides

Smaller polysaccharides,maltose

Polysaccharides

Maltose and otherdisaccharides

Disaccharides

Pancreatic amylases

Salivary amylase

Disaccharidases

Monosaccharides

(starch, glycogen) (sucrose, lactose)

Page 30: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-13b

Stomach

Lumen ofsmall intestine

Epitheliumof smallintestine(brushborder)

Protein digestion Proteins

Polypeptides

Smallerpolypeptides

Pancreatic trypsin andchymotrypsin

Pepsin

Dipeptidases, carboxypeptidase,and aminopeptidase

Monosaccharides

Small polypeptides

Amino acids

Pancreatic carboxypeptidase

Amino acids

Small peptides

Page 31: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-13c

Lumen ofsmall intestine

Epitheliumof smallintestine(brushborder)

Nucleic acid digestion

DNA, RNA

Nucleotides

Pancreaticnucleases

Nucleosidasesandphosphatases

Nucleosides

Nucleotidases

Nitrogenous bases,sugars, phosphates

Page 32: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-13d

Lumen ofsmall intestine

Fat digestion

Fat globules

Fat droplets

Pancreatic lipase

Bile salts

Glycerol, fattyacids, monoglycerides

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Mechanisms that help regulate body weight

Homeostatic mechanisms

Hormonessatiety center

Page 34: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Hormonal control of digestion

Secretinand CCK

Stomach

GallbladderLiver

+

Duodenum ofsmall intestine

Bile

Gastrin

Secretin

Pancreas

CCK

CCK

Key

Stimulation

Inhibition

+

+

++ –

Cholecystoknin

aa

FA

+

Chyme (fat) –

Page 35: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Hormonal control in the Digestive system: Gastric hormones

GASTRIN:

Secretion: By enteroendocrine (G) cells in gastric pits of the mucosa.

Stimulus: Stomach distention and acid pH of chyme causes Gastrin.

Action:– 1. increases HCl production in stomach– 2. increases gastric motility– 3. stimulates growth of gastric mucosa– 4. contract lower esophageal sphincter– 5. relaxes pyloric sphincter– 6. relaxes ileocecal sphincter

Page 36: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Hormonal control in the Digestive system: Gastric hormones

Somatostatin:生長抑制素Secretion: By enteroendocrine (D) cells in gastric pits of the mucosa in the pylorus.

Stimulus: continuously released, overridden by Gastrin and nerves

Action:– Inhibition of Gastrin production

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Hormonal control in the Digestive system: Small Intestinal hormones

SECRETIN:

Secretion: By Enteroendocrine (S) cells in the Crypts of Lieberkuhn of small intestine.

Stimulus: Acid chyme in small intestine causes secretion of Secretin:

Actions:– stimulate secretion of pancreatic juice and bile that is rich in

bicarbonate ions.

– inhibit production of HCl in stomach

– promote growth and maintenance of the pancreas

– enhance effects of Cholecystokinin (CCK)

– Increases rate of bile secretion by hepatocytes

所有 intestine 的 mucosa ,在 vili 之間仍然有向下凹的構造,稱為 crypt of Lieberkuhn 。

Page 38: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Hormonal control in the Digestive system: small intestinal hormones

CHOLECYSTOKININ (CCK):

Secretion: Enteroendocrine (CCK) cells in the small intestine mucosa Crypts of Lieberkuhn

Stimulus: Chyme rich in amino acids, triglycerides and fatty acids enter the small intestine.

Actions:– increases secretion of pancreatic juice rich in digestive

enzymes– opens the Sphincter of Oddi– contracts the gallbladder– Inhibits gastric secretion and motility– May reduce hunger

Page 39: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Hormonal control in the Digestive system: small intestinal hormones

Gastric Inhibitory Peptide (GIP):Secretion: Enteroendocrine cells in the small

intestine mucosa Crypts of Lieberkuhn

Stimulus: Chyme rich in triglycerides, fatty acids, and glucose enter the small intestine.

Actions:– Stimulates release of insulin by beta cells– Inhibits gastric secretion and motility– Stimulates lipogenesis by adipose tissue– Stimulates glucose use by skeletal muscle cells

Page 40: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Hormonal control in the Digestive system: small intestinal hormones

Vasoactive Intestinal Peptide (VIP):Secretion: Enteroendocrine cells in the small intestine mucosa Crypts of Lieberkuhn

Stimulus: Chyme entering the small intestine.

Actions:– Stimulates buffer secretion: H2O, electrolytes – Inhibits gastric secretion – Dilates intestinal capillaries

– stimulating pancreatic bicarbonate secretion,

Page 41: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

STOMACHHORMONAL CONTROL

CHEMICAL DIGESTION

1. Gastrin--stimulates gastric secretions

2. Histamine--stimulates HCl formation3. Somatostatin—inhibits gastric secretions4. Secretin--inhibits gastric secretions5. Gastric inhibiory peptide--inhibits gastric secretions6. Vasoactive intestinal peptide-inhibits HCl production

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LIVER GALLBLADDERNEUROLOGICAL CONTROLThe gallbladder is regulated by the autonomic nervous system. The parasympathetic division, using the vagus nerve, is excitatory and the sympathetic division inhibits the gallbladder.

HORMONAL CONTROL

The liver is stimulated by secretin to produce bile more rapidly. Cholecysto-kinin stimulates the gallbladder to contract and hepatopancreatic sphincter to relax, so that bile can enter the duodenum.

Page 43: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

PANCREAS

HORMONAL CONTROL

The pancreas is regulated hormonally by secretin and cholecystokinin (CCK). CCK induces the acinar cells to secrete the enzymes found in pancreatic juice. Secretin causes bicarbonate ions to form.

Page 44: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

segmentation

MECHANICAL DIGESTION

In segmentation, nonadjacentsegments of the intestinealternately contract andrelax, moving the chyme forward and then backwardresulting through mixing. Thisresults in the chyme being well mixed with the enzymes from the liver and the pancreas.

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peristalsis

PROPULSION 推動

Propulsion is the result of peristalsis. This causesadjacent segments to alternately contract and relax.

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- Adipocytes (fat cells) secrete

hormones (leptin) that regulate

appetite and body weight.

Role of Hormones in Appetite Regulation

- Hormones from GI:

cholecystokinin: suppressantghrelin: stimulantPYY: suppressant

(Science 299:846-849 2003)

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Fig. 41-23

LeptinPYY

Insulin

Ghrelin

The appetite –regulating hormoneby affecting a “satiety center’ in the brain

Lose weight, ghrelin increases

Body fat decreases, leptin levels fall

An appetite suppressant that counters the ghrelin

Suppresses appetite

Page 48: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

PYY and GhrelinPeptide YY is a short (36-amino acid) protein released by cells in the ileum and colon in response to feeding. In humans it appears to reduce appetite.

also known as PYY, Peptide Tyrosine Tyrosine, or Pancreatic Peptide YY3-36.[1]

PYY exerts its action through NPY receptors, inhibits and increases water and electrolyte absorption in the colon.[6] PYY may also suppress pancreatic secretion. It is secreted by the neuroendocrine cells in the ileum and colon

in response to a meal, and has been shown to reduce appetite. PYY works by slowing the gastric emptying; hence, it increases efficiency of digestion and nutrient absorption after meal.

Ghrelin is a hormone produced mainly by the fundus of the human stomach and pancreas that stimulates hunger.[1]

Ghrelin levels increase before meals and decrease after meals.

It is considered the counterpart of the hormone leptin, produced by adipose tissue, which induces satiation when present at higher levels.

In some bariatric procedures, the level of ghrelin is reduced in patients, thus causing satiation before it would normally occur.

Page 49: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Overnourishment and Obesity

Obesity

contributes to diabetes (type 2), cancer of the colon and breasts, heart attacks, and strokes

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Fig. 41-24a

Obese mouse with mutantob gene (left) next to wild-type mouse.

EXPERIMENT

OB /DB X Wild type

Coleman Revealed a Satiety Factor in Mammals

Ob+ gene:

produce leptin (the satiety factor)

Db+ gene:

produce leptin receptor

Parabiosis連體共生

Page 53: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

X

Feature Investigation

Page 54: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Fig. 41-24b

Ob+ gene:

leptin (the satiety factor)

Db+ gene:

leptin receptorMost obese humans like db mice –

produce leptin but fail to respond to it

Wild type

ob+, db+

X

ob+, db

Page 55: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

Leptin's effects. Because of a gene defect, the boy doesn't make leptin, but treatment with the hormone, begun when he was 3.5 years old (top), brought his weight down to normal levels, as shown at age 8.

(Science 299:846-849 2003)

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What if ?

There are two groups of obese people. In one group, the leptin levels are abnormally high; in the other group, they are abnormallyLow.

Q: How would each group’s leptin levels changes if both groups were placed on a low-calorie diet for an extended period? Explain.

Page 57: Fig. 41-1 Chapter 41 Animal Nutrition Taken in Taken apart Taken up

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